CA2307280A1 - Analyte assay using particulate labels - Google Patents
Analyte assay using particulate labels Download PDFInfo
- Publication number
- CA2307280A1 CA2307280A1 CA002307280A CA2307280A CA2307280A1 CA 2307280 A1 CA2307280 A1 CA 2307280A1 CA 002307280 A CA002307280 A CA 002307280A CA 2307280 A CA2307280 A CA 2307280A CA 2307280 A1 CA2307280 A1 CA 2307280A1
- Authority
- CA
- Canada
- Prior art keywords
- particle
- light
- particles
- scattered
- analyte
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54313—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being characterised by its particulate form
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6816—Hybridisation assays characterised by the detection means
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Electro-optical investigation, e.g. flow cytometers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/58—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
- G01N33/585—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with a particulate label, e.g. coloured latex
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Electro-optical investigation, e.g. flow cytometers
- G01N15/1425—Electro-optical investigation, e.g. flow cytometers using an analyser being characterised by its control arrangement
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Electro-optical investigation, e.g. flow cytometers
- G01N15/1456—Electro-optical investigation, e.g. flow cytometers without spatial resolution of the texture or inner structure of the particle, e.g. processing of pulse signals
- G01N15/1459—Electro-optical investigation, e.g. flow cytometers without spatial resolution of the texture or inner structure of the particle, e.g. processing of pulse signals the analysis being performed on a sample stream
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N2015/0038—Investigating nanoparticles
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/14—Electro-optical investigation, e.g. flow cytometers
- G01N2015/1493—Particle size
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/805—Optical property
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/817—Steroids or hormones
Abstract
Method for specific detection of one or more analytes in a sample. The method includes specifically associating any one or more analytes in the sample with a scattered-light detectable particle, illuminating any particle associated with the analytes with light under conditions which produce scattered light from the particle and in which light scattered from one or more particles can be detected by a human eye with less than 500 times magnification and without electronic amplification. The method also includes detecting the light scattered by any such particles under those conditions as a measure of the presence of the analytes.
Claims (63)
1. A method for selection of a particle type for detection of an analyte by light scattering, said method comprising the steps of:
a) providing light scattering signal strength versus particle size information for candidate particles; and b) selecting a particle of a size between 1 and 500 nm inclusive which provides acceptable dynamic range, acceptable low concentration detection sensitivity, and acceptable detection resolution based on said information, wherein the acceptable dynamic range, acceptable low concentration detection sensitivity, and acceptable detection resolution are determined by the concentration levels expected for said analyte in samples to be analyzed and are sufficient to allow non-evanescent light scattered from one or more said particles to be detected by a human eye with less than 500 times magnification and without electronic amplification.
a) providing light scattering signal strength versus particle size information for candidate particles; and b) selecting a particle of a size between 1 and 500 nm inclusive which provides acceptable dynamic range, acceptable low concentration detection sensitivity, and acceptable detection resolution based on said information, wherein the acceptable dynamic range, acceptable low concentration detection sensitivity, and acceptable detection resolution are determined by the concentration levels expected for said analyte in samples to be analyzed and are sufficient to allow non-evanescent light scattered from one or more said particles to be detected by a human eye with less than 500 times magnification and without electronic amplification.
2. The method of claim 1, wherein said detection of an analyte by light scattering is performed in a solid-phase assay, and said selecting further comprises identification of a light scattering particle which co-optimizes particle density and particle size, thereby providing a useful combination of signal strength and dynamic range.
3. The method of claim 2, wherein the light scattering signal consists of an integrated scattered light signal.
4. The method of claim 2, wherein the light scattering signal consists of light scattered from an individual particle or a single aggregate containing a plurality of particles.
5. The method of claim 1, wherein said detection of an analyte is performed in a liquid phase assay.
6. The method of claim 5, wherein the light scattering signal consists of an integrated scattered light signal.
7. The method of claim 5, wherein the light scattering signal consists of light scattered from an individual particle or a single aggregate containing a plurality of particles.
8. A method for specific detection of one or more analytes in a sample, comprising the steps of:
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive;
illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification; and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said particles or a multi-particle structure comprising a plurality of said particles is detected singly, wherein said particles are flowed by at least one detector.
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive;
illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification; and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said particles or a multi-particle structure comprising a plurality of said particles is detected singly, wherein said particles are flowed by at least one detector.
9. The method of claim 8, wherein said particles are flowed by said at least one detector in a structure selected from the group consisting of capillaries, microchannels, and spectrophotometric or flow cytometry flow cells.
10. The method of claim 8, wherein said analyte comprises a nucleic acid sequence, and at least one scattered light detectable particle is attached to at least two probe nucleic acid strands, wherein said at least two probe nucleic acid strands bind to different regions of said nucleic acid sequence; and said detecting further comprises flowing said nucleic acid sequences by the detector one at a time and distinguishing single particles from two or more particles, wherein detection of two or more particles is indicative of the presence of said nucleic acid sequence.
11. The method of claim 8, wherein said analyte comprises a cell or a cellular constituent and said detecting further comprises discriminating light scattering of said scattered light detectable particles from light scattering from said cell.
12. The method of claim 11, wherein said discriminating comprises providing two detectors such that the relative levels of cell specific light scattering and particle specific light scattering differ for said two detectors.
13. The method of claim 8, wherein said detecting provides a light scattering signal consisting of light scattered from an individual particle or a single aggregate containing a plurality of particles.
14. The method of claim 8, wherein said detecting provides a light scattering signal the characteristics which comprise at least one of intensity, polarization , wavelength, and angle of observation.
15. The method of claim 8, wherein said detecting provides a light scattering signal indicative of changes in one or more properties of the scattered light detectable properties of individual particles or multi-particle aggregates as said particles or aggregates move in a solution.
16. The method of claim 8, wherein a plurality of different particles with different sizes or compositions or both are distinguishably detected, each said different particle specifically associating with a different analyte.
17. A method for specific detection of one or more analytes in a sample, comprising the steps of:
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive;
illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification; and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said detecting comprises spatially discriminating or classifying or both scattered light from said particles, thereby separately identifying individual particles or mufti-particle structures.
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive;
illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification; and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said detecting comprises spatially discriminating or classifying or both scattered light from said particles, thereby separately identifying individual particles or mufti-particle structures.
18. The method of claim 17, wherein said discriminating or classifying comprises electronic image processing and analysis.
19. The method of claim 17, wherein said detection of an analyte by light scattering is performed in a solid-phase assay.
20. The method of claim 17, wherein said detection of an analyte is performed in a liquid phase assay.
21. The method of claim 17, wherein the characteristics of the light scattering signal measured comprise at least one of intensity, polarization, wavelength, and angle of observation.
22. The method of claim 17, wherein the light scattering signal measured detects changes in one or more properties of the scattered light detectable properties of individual particles or mufti-particle aggregates as said particles or aggregates move in a solution.
23. The method of claim 17, wherein a plurality of different particles with different sizes or compositions or both are distinguishably detected, each said different particle specifically associating with a different analyte.
24. A method for specific detection of one or more analytes in a sample, comprising the steps of:
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said scattered light detectable particles also possess magnetic or electrophoretic properties, and said properties are used to localize said particles during performance of an assay or to separate particles associated with any said one or more analytes from particles not so associated or both.
specifically associating any said one or more analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, illuminating any said particles associated with said analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more analytes, wherein said scattered light detectable particles also possess magnetic or electrophoretic properties, and said properties are used to localize said particles during performance of an assay or to separate particles associated with any said one or more analytes from particles not so associated or both.
25. The method of claim 24, wherein said detection of an analyte by light scattering is performed in a solid-phase assay.
26. The method of claim 24, wherein said detection of an analyte is performed in a liquid phase assay.
27. The method of claim 24, wherein the characteristics of the light scattering signal measured comprise at least one of intensity, polarization, wavelength, and angle of observation.
28. The method of claim 24, wherein the light scattering signal measured detects changes in one or more properties of the scattered light detectable properties of individual particles or multi-particle aggregates as said particles or aggregates move in a solution.
29. The method of claim 24, wherein a plurality of different particles with different sizes or compositions or both are distinguishably detected, each said different particle specifically associating with a different analyte.
30. A method for specific detection of one or more nucleic acid analytes comprising target nucleic acid sequences in a sample, comprising the steps of:
specifically associating any of said one or more nucleic acid analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, wherein said specific associating involves specific hybridization of at least one analyte-specific nucleic acid probe with any of said one or more nucleic acid analytes, wherein said particle is directly attached to a said probe or a said probe has a ligand for attachment of said particle, illuminating any said particles associated with said nucleic acid analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more nucleic acid analytes.
specifically associating any of said one or more nucleic acid analytes in said sample with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, wherein said specific associating involves specific hybridization of at least one analyte-specific nucleic acid probe with any of said one or more nucleic acid analytes, wherein said particle is directly attached to a said probe or a said probe has a ligand for attachment of said particle, illuminating any said particles associated with said nucleic acid analytes with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions as a measure of the presence of said one or more nucleic acid analytes.
31. The method of claim 30, wherein said detection of an analyte by light scattering is performed in a solid-phase assay.
32. The method of claim 30, wherein said detection of an analyte is performed in a liquid phase assay.
33. The method of claim 30, wherein said one or more nucleic acid analytes comprise a plurality of target nucleic acid sequences;
said plurality of nucleic acid analytes or a plurality of nucleic acid probes are attached in separate spots to a solid surface; and light scattering from one or more of said separate spots is detected as a measure of the presence or amount of at least one of said one or more nucleic acid analytes in said sample.
said plurality of nucleic acid analytes or a plurality of nucleic acid probes are attached in separate spots to a solid surface; and light scattering from one or more of said separate spots is detected as a measure of the presence or amount of at least one of said one or more nucleic acid analytes in said sample.
34. The method of claim 33, wherein determination of an integrated scattered light intensity of a said spot is used as an indicator of the amount of said nucleic acid analyte in said sample.
35. The method of claim 33, wherein the number of said scattered light detectable particles in at least a portion of a said spot is used as an indicator of the amount of a said nucleic acid analyte in said sample.
36. The method of claim 35, wherein the light scattering signals from individual scattered light detectable particles in said at least a portion of a said spot are summed to provide a summed light scattering signal indicative of the amount of a said nucleic acid analyte in said sample.
37. The method of claim 33, wherein light scattering from each said spot is detected by scanning of said separate spots.
38. The method of claim 33, wherein light scattering from each said spot is detected using separate detectors for each said spot.
39. The method of claim 33, wherein light scattering from each said spot is detected using simultaneous imaging of said plurality of spots.
40. The method of claim 39, wherein at least one image of said plurality of spots is analyzed using electronic image processing.
41. The method of claim 33, wherein said plurality of spots comprises an array.
42. The method of claim 41, wherein said array is adapted for sequencing by hybridization or determination of expression level of at least one nucleic acid sequence.
43. The method of claim 30 wherein a plurality of different particles with different sizes or compositions or both are distinguishably detected, each said different particle specifically associating with a different nucleic acid analyte.
44. A method for identifying the presence or amount of at least one cell type or organism in a sample, comprising detecting the presence or amount of at least one scattered light detectable particle of a size between 1 and 500 nm inclusive specifically associated with said at least one cell type or organism:
wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification, and light scattered by any of said at least one particle is detected as a measure of the presence or amount of any of said at least one cell type or organism.
wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification, and light scattered by any of said at least one particle is detected as a measure of the presence or amount of any of said at least one cell type or organism.
45. The method of claim 44, wherein said identifying the amount of said cell type or organism further comprises determining the amount of cells or organisms with at least one of said particles specifically associated with said cell or organism relative to cells or organisms without said at least one of said particles specifically associated therewith.
46. The method of claim 44, wherein the presence or amount of at least one of a plurality of different yell types or organisms is distinguished or identified using a plurality of different particle types, wherein each of said plurality of different particle types specifically associates with a different cell type or organism, and the light scattering signal from each of said plurality of different particle types is distinguishable from each of the other particle types of said plurality of different particle types.
47. The method of claim 44, wherein the presence or amount of at least one of a plurality of different cell types or organisms is distinguished or identified using a plurality of different particle types, wherein each of said plurality of different particle types specifically associates with at least one of said plurality of different cell types or organisms, and the light scattering signal from each of said plurality of different particle types is distinguishable from each of the other particle types of said plurality of different particle types.
48. The method of claim 44, wherein said determining the presence or amount of at least one cell type or organism comprises identifying said at least one cell type or organism.
49. The method of claim 44, wherein said particle is intracellular.
50. The method of claim 44, wherein a said particle comprises gold or silver or both.
51. A method for detecting the presence or amount of at least one analyte in a cell type or organism, comprising the step of detecting the presence or amount of at least one scattered light detectable particle of a size between 1 and 500 nm inclusive specifically associated with said at least one cell type or organism:
wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification, and light scattered by any of said at least one particle is detected as a measure of the presence or amount of said at least one analyte in a said cell type or organism.
wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification, and light scattered by any of said at least one particle is detected as a measure of the presence or amount of said at least one analyte in a said cell type or organism.
52. The method of claim 51, wherein at least one said analyte is an intracellular protein.
53. The method of claim 51, wherein said at least one analyte is a plurality of analytes, and said at least one scattered light detectable particle is a plurality of distinguishable particles.
54. A method for monitoring a cell or organism, comprising the steps of:
placing at least one scattered light detectable particle of a size between 1 and 500 nm inclusive within a cell; and detecting the presence of at least one said scattered light detectable particle within said cell or organism as an indication of the presence of said cell or organism, wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification.
placing at least one scattered light detectable particle of a size between 1 and 500 nm inclusive within a cell; and detecting the presence of at least one said scattered light detectable particle within said cell or organism as an indication of the presence of said cell or organism, wherein said at least one scattered light detectable particle is illuminated with non-evanescent wave light under conditions which produce scattered light from said at least one particle and in which light scattered from said at least one particle can be detected by a human eye with less than 500 times magnification and without electronic amplification.
55. A method for identifying or characterizing a potential pharmaceutical agent, comprising the steps of:
screening a library comprising a plurality of potential targets or a plurality of potential pharmaceutical agents to detect an interaction between a target and a said potential pharmaceutical agent, wherein said screening comprises specifically associating any of said plurality of potential targets or potential pharmaceutical agents or an expression product or mRNA with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, illuminating any said particles associated with any said plurality of potential targets or potential pharmaceutical agents or expression product or mRNA with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions such that detection of said light is indicative of a said interaction.
screening a library comprising a plurality of potential targets or a plurality of potential pharmaceutical agents to detect an interaction between a target and a said potential pharmaceutical agent, wherein said screening comprises specifically associating any of said plurality of potential targets or potential pharmaceutical agents or an expression product or mRNA with a scattered-light detectable particle of a size between 1 and 500 nm inclusive, illuminating any said particles associated with any said plurality of potential targets or potential pharmaceutical agents or expression product or mRNA with non-evanescent wave light under conditions which produce scattered light from said particle and in which light scattered from one or more said particles can be detected by a human eye with less than 500 times magnification and without electronic amplification, and detecting said light scattered by any said particles under said conditions such that detection of said light is indicative of a said interaction.
56. The method of claim 55, wherein said interaction comprises a binding interaction between a target or potential target and a said potential pharmaceutical agent.
57. The method of claim 55, wherein said interaction comprises modulation of a drug target system.
58. The method of claim 57, wherein said determination of said modulation comprises determination of the level of expression of a component of said system.
59. The method of claim 55, wherein said detecting said light scattered by any said particles is performed in a homogeneous assay.
60. The method of claim 55, wherein said plurality of potential targets or plurality of potential pharmaceutical agents is in a spatially addressable library.
61. The method of claim 55, wherein each of said plurality of potential pharmaceutical agents is attached to a solid substrate particle.
62. The method of claim 61, wherein a said scattered-light detectable particle also comprise a magnetic or ferro-electric composition, and said method further comprises manipulating the position of said particles associated with a said potential pharmaceutical agent attached to a said solid substrate particle.
63. The method of claim 55, wherein the amount of said expression product or mRNA is altered by said interaction.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2719432A CA2719432A1 (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/953,713 US6586193B2 (en) | 1996-04-25 | 1997-10-17 | Analyte assay using particulate labels |
US08/953,713 | 1997-10-17 | ||
PCT/US1998/023160 WO1999020789A1 (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2719432A Division CA2719432A1 (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2307280A1 true CA2307280A1 (en) | 1999-04-29 |
CA2307280C CA2307280C (en) | 2010-12-14 |
Family
ID=25494434
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2719432A Abandoned CA2719432A1 (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
CA2307280A Expired - Fee Related CA2307280C (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2719432A Abandoned CA2719432A1 (en) | 1997-10-17 | 1998-10-16 | Analyte assay using particulate labels |
Country Status (11)
Country | Link |
---|---|
US (7) | US6586193B2 (en) |
EP (1) | EP1023456A1 (en) |
JP (1) | JP4247770B2 (en) |
CN (1) | CN100379876C (en) |
AU (1) | AU1294399A (en) |
BR (1) | BR9814821A (en) |
CA (2) | CA2719432A1 (en) |
HK (1) | HK1034291A1 (en) |
IL (1) | IL135696A (en) |
RU (1) | RU2217498C2 (en) |
WO (1) | WO1999020789A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109957503A (en) * | 2017-12-14 | 2019-07-02 | 长光华大基因测序设备(长春)有限公司 | A kind of processing chip and its application for high-throughput gene sequencing equipment |
Families Citing this family (253)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6586193B2 (en) * | 1996-04-25 | 2003-07-01 | Genicon Sciences Corporation | Analyte assay using particulate labels |
US6506564B1 (en) | 1996-07-29 | 2003-01-14 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
US6361944B1 (en) | 1996-07-29 | 2002-03-26 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
US6582921B2 (en) | 1996-07-29 | 2003-06-24 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses thereof |
ES2287956T3 (en) | 1996-07-29 | 2007-12-16 | Nanosphere Inc. | NANOPARTICLES THAT HAVE OLIGONUCLEOTIDES UNITED TO THE SAME AND USES OF THE SAME. |
US6984491B2 (en) | 1996-07-29 | 2006-01-10 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
US7098320B1 (en) | 1996-07-29 | 2006-08-29 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
US6750016B2 (en) | 1996-07-29 | 2004-06-15 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
US6974669B2 (en) | 2000-03-28 | 2005-12-13 | Nanosphere, Inc. | Bio-barcodes based on oligonucleotide-modified nanoparticles |
EP1060455A4 (en) * | 1998-02-10 | 2002-08-07 | Ey Lab Inc | Reflectometry system with compensation for specimen holder topography and with lock-rejection of system noise |
US20030153023A1 (en) * | 1999-05-13 | 2003-08-14 | Starzl Timothy W. | Enumeration method of analyte detection |
AU1219800A (en) * | 1998-10-20 | 2000-05-08 | Ljl Biosystems, Inc. | Improvements in luminescence assays |
US20030096321A1 (en) * | 1999-05-19 | 2003-05-22 | Jose Remacle | Method for the identification and/or the quantification of a target compound obtained from a biological sample upon chips |
WO2001051665A2 (en) | 2000-01-13 | 2001-07-19 | Nanosphere Inc. | Nanoparticles having oligonucleotides attached thereto and uses therefor |
WO2001071322A2 (en) * | 2000-03-22 | 2001-09-27 | Goh M Cynthia | Method and apparatus for multiple-analyte assay |
US7829313B2 (en) | 2000-03-24 | 2010-11-09 | Eppendorf Array Technologies | Identification and quantification of a plurality of biological (micro)organisms or their components |
US7875442B2 (en) | 2000-03-24 | 2011-01-25 | Eppendorf Array Technologies | Identification and quantification of a plurality of biological (micro)organisms or their components |
US8288128B2 (en) | 2004-11-18 | 2012-10-16 | Eppendorf Array Technologies S.A. | Real-time quantification of multiple targets on a micro-array |
WO2001090748A2 (en) * | 2000-05-19 | 2001-11-29 | Iowa State University Research Foundation, Inc. | High-throughput methods of distinguishing at least one molecule individually in a sample comprising multiple molecules and systems for use therein |
US6784981B1 (en) | 2000-06-02 | 2004-08-31 | Idexx Laboratories, Inc. | Flow cytometry-based hematology system |
AU2001275475A1 (en) * | 2000-06-12 | 2001-12-24 | Genicon Sciences Corporation | Assay for genetic polymorphisms using scattered light detectable labels |
US6602669B2 (en) | 2000-07-11 | 2003-08-05 | Northwestern University | Method of detection by enhancement of silver staining |
EP1319179B1 (en) * | 2000-07-19 | 2008-03-05 | Genisphere Inc. | Methods for detecting and assaying nucleic acid sequences |
US20020049682A1 (en) * | 2000-09-01 | 2002-04-25 | Nobuko Yamamoto | Authentication certificate, authentication certificate issuance system, and authentication system |
WO2002025630A2 (en) * | 2000-09-20 | 2002-03-28 | Molecular Reflections | Microfabricated ultrasound array for use as resonant sensors |
WO2002029411A2 (en) * | 2000-10-03 | 2002-04-11 | Minerva Biotechnologies Corporation | Magnetic in situ dilution |
US20030175994A1 (en) * | 2000-10-05 | 2003-09-18 | Yoram Palti | Geometrically efficient particle agglutination, particularly to detect low affinity |
WO2002040998A2 (en) * | 2000-11-17 | 2002-05-23 | Zeptosens Ag | Kit and method for determining multiple analytes |
WO2002068932A2 (en) * | 2001-02-23 | 2002-09-06 | Genicon Sciences Corporation | Methods for providing extended dynamic range in analyte assays |
FR2824001B1 (en) * | 2001-04-26 | 2003-10-10 | Bio Merieux | METHOD FOR DEPOSITING A SPOT OF A PRODUCT OF INTEREST, AND APPLICATION FOR ISOLATING AND / OR DETERMINING AN ANALYTE |
US20040166593A1 (en) * | 2001-06-22 | 2004-08-26 | Nolte David D. | Adaptive interferometric multi-analyte high-speed biosensor |
US20040161741A1 (en) * | 2001-06-30 | 2004-08-19 | Elazar Rabani | Novel compositions and processes for analyte detection, quantification and amplification |
US6714299B2 (en) | 2001-07-13 | 2004-03-30 | Genicon Sciences Corporation | Use of light scattering particles in design, manufacture, and quality control of small volume instruments, devices, and processes |
US20030013083A1 (en) * | 2001-07-16 | 2003-01-16 | Tsai Tenlin S. | Particle analysis as a detection system for particle-enhanced assays |
WO2003021231A2 (en) * | 2001-09-05 | 2003-03-13 | Genicon Sciences Corporation | Method and apparatus for normalization and deconvolution of assay data |
US20030049866A1 (en) * | 2001-09-05 | 2003-03-13 | Genicon Sciences Corporation | Sample device preservation |
CA2460212C (en) | 2001-09-06 | 2013-01-22 | Genomic Profiling Systems, Inc. | Rapid and sensitive detection of cells and viruses |
JP3685119B2 (en) * | 2001-10-18 | 2005-08-17 | 株式会社日立製作所 | Biomolecule recovery method |
WO2003081202A2 (en) | 2001-11-09 | 2003-10-02 | Nanosphere, Inc. | Bioconjugate-nanoparticle probes |
JP2005509871A (en) * | 2001-11-20 | 2005-04-14 | エグザクト サイエンシーズ コーポレイション | Automated sample preparation method and apparatus |
GR1004178B (en) * | 2001-11-29 | 2003-03-05 | "����������" | Integrated optoelectronic silicon biosensor for the detection of biomolecules labeled with chromophore groups or nanoparticles |
JP3856214B2 (en) * | 2002-03-11 | 2006-12-13 | 横河電機株式会社 | Fluorescence intensity enhancement beads |
US20040038264A1 (en) * | 2002-05-14 | 2004-02-26 | Souza Glauco R. | Fractal dimension analysis of nanoparticle aggregates using angle dependent light scattering for the detection and characterization of nucleic acids and proteins |
KR20040044336A (en) * | 2002-11-12 | 2004-05-28 | 마쯔시다덴기산교 가부시키가이샤 | Specific coupling reaction measuring method and reagent kit and specific coupling reaction measuring apparatus for use in the same |
WO2004046100A2 (en) * | 2002-11-15 | 2004-06-03 | University Of Maryland, Baltimore | Release of the self-quenching of fluorescence near silver metallic surfaces |
JP2004184312A (en) * | 2002-12-05 | 2004-07-02 | Yokogawa Electric Corp | Biopolymer detection method and biochip |
US7053783B2 (en) | 2002-12-18 | 2006-05-30 | Biovigilant Systems, Inc. | Pathogen detector system and method |
AU2003292599A1 (en) * | 2002-12-20 | 2004-07-14 | Shigeki Higashiyama | Method of screening cell growth inhibitor and cell growth inhibitor |
JP4740111B2 (en) * | 2003-02-13 | 2011-08-03 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Methods and compositions for detecting and analyzing polynucleotide binding protein interactions using light collecting multichromophores |
US20080050842A1 (en) * | 2003-02-15 | 2008-02-28 | Golovlev Valeri V | Method of visualization and quanitification of biopolymer molecules immobilized on solid support |
US20040161862A1 (en) * | 2003-02-15 | 2004-08-19 | Golovlev Valeri V. | Method of visualization and quantification of biopolymer molecules immobilized on solid support |
JP2007524347A (en) * | 2003-02-27 | 2007-08-30 | ナノスフェアー インコーポレイテッド | Label-free gene expression profiling using universal nanoparticle probes in microarray format assays |
US7341841B2 (en) * | 2003-07-12 | 2008-03-11 | Accelr8 Technology Corporation | Rapid microbial detection and antimicrobial susceptibility testing |
AU2004273783A1 (en) | 2003-07-12 | 2005-03-31 | Accelr8 Technology Corporation | Sensitive and rapid biodetection |
US20120077206A1 (en) | 2003-07-12 | 2012-03-29 | Accelr8 Technology Corporation | Rapid Microbial Detection and Antimicrobial Susceptibility Testing |
US7641971B2 (en) * | 2003-08-13 | 2010-01-05 | Crane Company | Metal-treated particles for remediation |
US20060035242A1 (en) | 2004-08-13 | 2006-02-16 | Michelitsch Melissa D | Prion-specific peptide reagents |
US7352467B2 (en) * | 2003-10-24 | 2008-04-01 | University Of Washington | Surface plasmon resonance imaging system and method |
US20050112586A1 (en) * | 2003-11-24 | 2005-05-26 | Roland Janzen | Method and composition for stabilizing liquid reagents |
US7329391B2 (en) * | 2003-12-08 | 2008-02-12 | Applera Corporation | Microfluidic device and material manipulating method using same |
WO2005066613A1 (en) | 2003-12-31 | 2005-07-21 | President And Fellows Of Harvard College | Assay device and method |
US20050141843A1 (en) * | 2003-12-31 | 2005-06-30 | Invitrogen Corporation | Waveguide comprising scattered light detectable particles |
AU2005207302B2 (en) * | 2004-01-14 | 2010-05-20 | Luminex Corporation | Methods for altering one or more parameters of a measurement system |
CN102357352B (en) | 2004-01-26 | 2015-08-12 | 哈佛大学 | Fluid delivery system and method |
US8030057B2 (en) * | 2004-01-26 | 2011-10-04 | President And Fellows Of Harvard College | Fluid delivery system and method |
CN1667418B (en) * | 2004-03-10 | 2010-10-06 | 马杰 | Multifunctional portable unit for measurement, analysis and diagnosis |
US7623234B2 (en) * | 2004-03-22 | 2009-11-24 | Quantaspec, Inc. | System and method for detecting and identifying an analyte |
US20070095393A1 (en) * | 2004-03-30 | 2007-05-03 | Piero Zucchelli | Devices and methods for programmable microscale manipulation of fluids |
US7771660B2 (en) * | 2004-05-04 | 2010-08-10 | University Of North Carolina At Chapel Hill | Electrophoretic interactive spectral methods and devices for the detection and/or characterization of biological particles |
AU2005246415B8 (en) | 2004-05-19 | 2011-09-01 | Vp Holding, Llc | Optical sensor with layered plasmon structure for enhanced detection of chemical groups by SERS |
US20050287680A1 (en) * | 2004-06-25 | 2005-12-29 | Srivatsa Venkatasubbarao | Multianalyte assay method |
KR101170859B1 (en) | 2004-07-30 | 2012-08-02 | 바이오비질런트 시스템즈 인코포레이티드 | Pathogen and particle detector system and method |
US20060024815A1 (en) * | 2004-07-30 | 2006-02-02 | Allman Steve L | High sensitivity array-based detection system |
US7750352B2 (en) * | 2004-08-10 | 2010-07-06 | Pinion Technologies, Inc. | Light strips for lighting and backlighting applications |
US20060046279A1 (en) * | 2004-08-24 | 2006-03-02 | Truong Palestrina R | Analytical methods utilizing real-time energy/particle interaction-based determination techniques |
US9494581B2 (en) | 2004-08-24 | 2016-11-15 | University Of Wyoming | System and method for Raman spectroscopy assay using paramagnetic particles |
EP1808407B1 (en) * | 2004-09-30 | 2014-12-31 | Japan Science and Technology Agency | Method of patterning self-organizing material, patterned substrate of self-organizing material and method of producing the same, and phosomask using patterned substrate of self-organizing material |
WO2006076683A2 (en) * | 2005-01-13 | 2006-07-20 | Novartis Vaccines And Diagnostics Inc. | Isolation and detection of pathogenic prions |
US20070023643A1 (en) * | 2005-02-01 | 2007-02-01 | Nolte David D | Differentially encoded biological analyzer planar array apparatus and methods |
US7910356B2 (en) * | 2005-02-01 | 2011-03-22 | Purdue Research Foundation | Multiplexed biological analyzer planar array apparatus and methods |
US7405831B2 (en) * | 2005-02-01 | 2008-07-29 | Purdue Research Foundation | Laser scanning interferometric surface metrology |
WO2006105110A2 (en) * | 2005-03-29 | 2006-10-05 | Inverness Medical Switzerland Gmbh | Assay device and methods |
US7300631B2 (en) * | 2005-05-02 | 2007-11-27 | Bioscale, Inc. | Method and apparatus for detection of analyte using a flexural plate wave device and magnetic particles |
US7749445B2 (en) * | 2005-05-02 | 2010-07-06 | Bioscale, Inc. | Method and apparatus for analyzing bioprocess fluids |
US7611908B2 (en) * | 2005-05-02 | 2009-11-03 | Bioscale, Inc. | Method and apparatus for therapeutic drug monitoring using an acoustic device |
US7991242B2 (en) | 2005-05-11 | 2011-08-02 | Optosecurity Inc. | Apparatus, method and system for screening receptacles and persons, having image distortion correction functionality |
CA2608119A1 (en) | 2005-05-11 | 2006-11-16 | Optosecurity Inc. | Method and system for screening luggage items, cargo containers or persons |
US20070036026A1 (en) * | 2005-05-16 | 2007-02-15 | Laibinis Paul E | Magnetic Particle Systems and Methods |
US20070081163A1 (en) * | 2005-06-03 | 2007-04-12 | Minhua Liang | Method and apparatus for scanned beam microarray assay |
CN101223560B (en) * | 2005-07-15 | 2012-12-12 | 百维吉伦特系统有限公司 | Pathogen and particle detector system and method |
US20070031282A1 (en) * | 2005-08-04 | 2007-02-08 | Piero Zucchelli | Devices and methods for interfacing microfluidic devices with fluid handling devices |
US20070030482A1 (en) * | 2005-08-08 | 2007-02-08 | Zhenghua Ji | Spectrophotometer with adjustable light pathlength |
US7791728B2 (en) | 2005-08-11 | 2010-09-07 | Hewlett-Packard Development Company, L.P. | System for optically analyzing a substance with a selected single-wavelength |
US20070134685A1 (en) * | 2005-09-06 | 2007-06-14 | Invitrogen Corporation | Control of chemical modification |
NZ566020A (en) | 2005-09-09 | 2012-08-31 | Novartis Ag | Prion-specific peptoid reagents |
US20120231453A1 (en) * | 2005-09-13 | 2012-09-13 | Affymetrix, Inc. | Brownian Microbarcodes for Bioassays |
EP2485052B1 (en) * | 2005-09-13 | 2015-05-06 | Affymetrix, Inc. | Encoded microparticles |
WO2007038478A2 (en) | 2005-09-26 | 2007-04-05 | Rapid Micro Biosystems, Inc | Cassette containing growth medium |
CA2632261A1 (en) * | 2005-12-05 | 2007-06-14 | Guava Technologies | Particle-based analyte characterization |
US7463358B2 (en) | 2005-12-06 | 2008-12-09 | Lumera Corporation | Highly stable surface plasmon resonance plates, microarrays, and methods |
FI120560B (en) * | 2005-12-21 | 2009-11-30 | Outotec Oyj | Method for determining elemental and / or mineral content |
JP2009524832A (en) | 2006-01-24 | 2009-07-02 | ライフ テクノロジーズ コーポレーション | Device and method for quantifying analytes |
US8460879B2 (en) | 2006-02-21 | 2013-06-11 | The Trustees Of Tufts College | Methods and arrays for target analyte detection and determination of target analyte concentration in solution |
JP2009530598A (en) * | 2006-03-17 | 2009-08-27 | ビバクタ、リミテッド | Chemical detector |
WO2007131103A2 (en) * | 2006-05-03 | 2007-11-15 | Quadraspec, Inc. | Direct printing of patterned hydrophobic wells |
ATE514086T1 (en) | 2006-05-09 | 2011-07-15 | Koninkl Philips Electronics Nv | DETECTION OF TARGET MOLECULES IN A SAMPLE USING A MAGNETIC FIELD |
US7899232B2 (en) | 2006-05-11 | 2011-03-01 | Optosecurity Inc. | Method and apparatus for providing threat image projection (TIP) in a luggage screening system, and luggage screening system implementing same |
KR20090027643A (en) * | 2006-05-17 | 2009-03-17 | 루미넥스 코포레이션 | Chip-based flow cytometer type systems for analyzing fluorescently tagged particles |
US7531774B2 (en) * | 2006-06-05 | 2009-05-12 | General Dynamics Advanced Information Systems, Inc. | Measurement-diverse imaging and wavefront sensing with amplitude and phase estimation |
US20100035243A1 (en) * | 2006-07-10 | 2010-02-11 | Nanosphere, Inc. | Ultra-sensitive detection of analytes |
JP4756270B2 (en) * | 2006-07-13 | 2011-08-24 | 独立行政法人産業技術総合研究所 | Optical spectroscopy measurement method and apparatus |
US8494210B2 (en) | 2007-03-30 | 2013-07-23 | Optosecurity Inc. | User interface for use in security screening providing image enhancement capabilities and apparatus for implementing same |
EP2059811A2 (en) * | 2006-08-18 | 2009-05-20 | 3M Innovative Properties Company | Methods of detection using acousto-mechanical detection systems |
US8207509B2 (en) * | 2006-09-01 | 2012-06-26 | Pacific Biosciences Of California, Inc. | Substrates, systems and methods for analyzing materials |
JP5151097B2 (en) * | 2006-09-01 | 2013-02-27 | 株式会社リコー | Composite metal nanoparticles, multiphoton absorption reaction materials and reaction products containing composite metal nanoparticles, and multiphoton absorption reaction aids containing composite metal nanoparticles |
US20080230605A1 (en) * | 2006-11-30 | 2008-09-25 | Brian Weichel | Process and apparatus for maintaining data integrity |
US20080144899A1 (en) * | 2006-11-30 | 2008-06-19 | Manoj Varma | Process for extracting periodic features from images by template matching |
US7522282B2 (en) * | 2006-11-30 | 2009-04-21 | Purdue Research Foundation | Molecular interferometric imaging process and apparatus |
US20100151553A1 (en) * | 2006-12-29 | 2010-06-17 | Bjork Jason W | Method of detection of bioanalytes by acousto-mechanical detection systems comprising the addition of liposomes |
WO2008088249A1 (en) * | 2007-01-17 | 2008-07-24 | Hemocue Ab | Apparatus for determining positions of objects contained in a sample |
SE530789C2 (en) * | 2007-01-17 | 2008-09-09 | Hemocue Ab | Apparatus and method for position determination of objects contained in a sample |
WO2008089495A2 (en) | 2007-01-19 | 2008-07-24 | Purdue Research Foundation | System with extended range of molecular sensing through integrated multi-modal data acquisition |
CA2681722A1 (en) * | 2007-03-26 | 2008-10-02 | Purdue Research Foundation | Method and apparatus for conjugate quadrature interferometric detection of an immunoassay |
CN101754812B (en) | 2007-05-04 | 2013-06-26 | 克拉洛诊断仪器公司 | Fluidic connectors and microfluidic systems |
JP4803125B2 (en) * | 2007-05-10 | 2011-10-26 | ソニー株式会社 | Bead group, method for producing the bead group, and method using the bead group |
US9199247B2 (en) * | 2007-05-29 | 2015-12-01 | Invitrogen Dynal As | Magnetic separation rack |
GB0724404D0 (en) | 2007-05-29 | 2008-01-30 | Invitrogen Dynal As | A sample vessel retaining portion |
US8094307B2 (en) * | 2007-07-05 | 2012-01-10 | Baxter International Inc. | Method and apparatus for measuring the presence and concentration of pharmaceutical substances in a medical fluid administered by a medication delivery system |
US8354280B2 (en) | 2007-09-06 | 2013-01-15 | Bioscale, Inc. | Reusable detection surfaces and methods of using same |
US8384033B2 (en) * | 2007-11-09 | 2013-02-26 | The Royal Institute For The Advancement Of Learning/Mcgill University | Quantification of an absorber through a scattering medium |
US20100323457A1 (en) * | 2007-12-03 | 2010-12-23 | Tokyo Institute Of Technology | Biosensing method using coated magnetic fine particles and biosensing apparatus for biosensing method |
US8628976B2 (en) * | 2007-12-03 | 2014-01-14 | Azbil BioVigilant, Inc. | Method for the detection of biologic particle contamination |
US8004669B1 (en) | 2007-12-18 | 2011-08-23 | Plexera Llc | SPR apparatus with a high performance fluid delivery system |
WO2009081406A2 (en) * | 2007-12-26 | 2009-07-02 | Yissum, Research Development Company Of The Hebrew University Of Jerusalem | Method and apparatus for monitoring processes in living cells |
CA2711151A1 (en) | 2008-01-03 | 2009-09-24 | University Of Central Florida Research Foundation, Inc. | Detection of analytes using metal nanoparticle probes and dynamic light scattering |
KR100962290B1 (en) * | 2008-02-13 | 2010-06-11 | 성균관대학교산학협력단 | Method of detecting bioproducts using localized surface plasmon resonance sensor of gold nanoparticles |
JP5344828B2 (en) * | 2008-02-28 | 2013-11-20 | 富士フイルム株式会社 | Sensing device |
US8008068B2 (en) * | 2008-02-29 | 2011-08-30 | Light Pointe Medical, Inc. | Nonhemolytic optical sensor with enhanced reflectance |
US20090219509A1 (en) * | 2008-02-29 | 2009-09-03 | Hiroshi Nomura | Optical sensor with enhanced reflectance |
KR20100135797A (en) | 2008-03-12 | 2010-12-27 | 유니버시티 오브 버지니아 페이턴트 파운데이션 | Detection of polymeric analytes |
US7995854B2 (en) * | 2008-03-28 | 2011-08-09 | Tandent Vision Science, Inc. | System and method for identifying complex tokens in an image |
EP2285491A1 (en) | 2008-04-25 | 2011-02-23 | Claros Diagnostics, Inc. | Flow control in microfluidic systems |
US20110189692A1 (en) * | 2008-04-30 | 2011-08-04 | Novartis Ag | Assay for pathogenic conformers |
US7796256B2 (en) * | 2008-05-05 | 2010-09-14 | Fluid Imaging Technologies, Inc. | Oil-immersion enhanced imaging flow cytometer |
WO2010008870A1 (en) * | 2008-06-24 | 2010-01-21 | Estill, James, A. | Small angle light scattering assay system and method for detecting malaria infection |
DE102008035770A1 (en) * | 2008-07-31 | 2010-02-18 | Eads Deutschland Gmbh | Optical particle detector and detection method |
US9151943B2 (en) | 2008-08-04 | 2015-10-06 | Fluid Imaging Technologies, Inc. | System and method for monitoring birefringent particles in a fluid |
US8345239B1 (en) | 2008-08-04 | 2013-01-01 | Fluid Imaging Technologies, Inc. | System and method for monitoring birefringent particles in a fluid |
TW201017149A (en) | 2008-08-06 | 2010-05-01 | Invitrox Inc | Use of focused light scattering techniques in biological applications |
DK3629011T3 (en) | 2008-09-16 | 2024-01-29 | Pacific Biosciences California Inc | INTEGRATED OPTICAL DEVICE |
US11865534B2 (en) | 2008-09-24 | 2024-01-09 | First Light Diagnostics, Inc. | Imaging analyzer for testing analytes |
US20100099076A1 (en) * | 2008-10-16 | 2010-04-22 | Kent State University | Sensitive and rapid detection of viral particles in early viral infection by laser tweezers |
DK2376226T3 (en) | 2008-12-18 | 2018-10-15 | Opko Diagnostics Llc | IMPROVED REAGENT STORAGE IN MICROFLUIDIC SYSTEMS AND RELATED ARTICLES AND PROCEDURES |
CA2647953A1 (en) * | 2008-12-29 | 2010-06-29 | Sqi Diagnostics Systems Inc. | Multiplex analyte detection |
DK2391451T3 (en) | 2009-02-02 | 2018-10-15 | Opko Diagnostics Llc | STRUCTURES FOR MANAGING LIGHT INTERACTION WITH MICROFLUIDIC DEVICES |
EP2223650A1 (en) * | 2009-02-25 | 2010-09-01 | The Provost, Fellows and Scholars of the College of the Holy and Undivided Trinity of Queen Elizabeth near Dublin | Method and apparatus for imaging tissue topography |
JP2012519170A (en) | 2009-02-26 | 2012-08-23 | オーエスアイ・ファーマシューティカルズ,エルエルシー | INSITU method for monitoring EMT status of tumor cells in vivo |
GB0904934D0 (en) * | 2009-03-23 | 2009-05-06 | Geneseqe As | Method and apparatus for detecting molecules |
US8477186B2 (en) * | 2009-04-06 | 2013-07-02 | Sumco Corporation | Apparatus for removing reflected light |
WO2010120686A2 (en) * | 2009-04-13 | 2010-10-21 | Parsons J Kellogg | Methods for the diagnosis and treatment of benign prostatic hyperplasia |
US8153987B2 (en) * | 2009-05-22 | 2012-04-10 | Jordan Valley Semiconductors Ltd. | Automated calibration methodology for VUV metrology system |
WO2011056215A1 (en) * | 2009-11-03 | 2011-05-12 | Landers James P | Versatile, visible method for detecting polymeric analytes |
WO2011057029A1 (en) | 2009-11-04 | 2011-05-12 | Novartis Ag | Positively charged species as binding reagents in the separation of protein aggregates from monomers |
HUE053571T2 (en) | 2009-11-24 | 2021-07-28 | Opko Diagnostics Llc | Fluid mixing and delivery in microfluidic systems |
KR101422573B1 (en) * | 2009-11-26 | 2014-07-25 | 삼성전자 주식회사 | Centrifugal Micro-fluidic Device and Method to measure biological makers from liquid specimen |
CN102667447B (en) * | 2009-11-30 | 2016-03-23 | 通用电气健康护理生物科学股份公司 | For the method and system that bonding behavior is analyzed |
US10545090B2 (en) * | 2009-11-30 | 2020-01-28 | Ge Healthcare Bio-Sciences Ab | Method and system for more reliable determination of interaction parameters for low affinity analytes |
US9339813B2 (en) | 2009-12-18 | 2016-05-17 | Koninklijke Philips N.V. | Substance determining apparatus |
US20110223587A1 (en) * | 2010-03-11 | 2011-09-15 | Schulman Joseph D | Optical particle characterization system |
US20110223586A1 (en) * | 2010-03-11 | 2011-09-15 | David Karabinus | Optical particle characterization system |
EP2369325A1 (en) | 2010-03-12 | 2011-09-28 | Eppendorf Ag | Array analysis for online detection |
CN102971629B (en) * | 2010-04-15 | 2016-10-12 | 数码传感有限公司 | Microarray |
CA3016967C (en) | 2010-04-16 | 2021-08-31 | Opko Diagnostics, Llc | Systems and devices for analysis of samples |
WO2011140387A1 (en) | 2010-05-05 | 2011-11-10 | Blue Ocean Biomedical, Llc | Diagnostic instrument and flow process |
USD645971S1 (en) | 2010-05-11 | 2011-09-27 | Claros Diagnostics, Inc. | Sample cassette |
US20130260396A1 (en) | 2010-05-25 | 2013-10-03 | Arryx, Inc. | Holographic fluctuation microscopy apparatus and method for determining mobility of particle and/or cell dispersions |
WO2012032955A1 (en) * | 2010-09-10 | 2012-03-15 | オリンパス株式会社 | Optical analysis method using optical measurement in multiple wavelength bands |
JP5945506B2 (en) * | 2010-11-25 | 2016-07-05 | オリンパス株式会社 | Optical analysis apparatus and optical analysis method using wavelength characteristics of light of single luminescent particles |
KR102523324B1 (en) | 2011-02-16 | 2023-04-18 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | Light-emitting element |
CN103492859B (en) * | 2011-02-28 | 2017-05-24 | 皇家飞利浦有限公司 | Substance determining apparatus |
US10254204B2 (en) | 2011-03-07 | 2019-04-09 | Accelerate Diagnostics, Inc. | Membrane-assisted purification |
ES2551922T3 (en) | 2011-03-07 | 2015-11-24 | Accelerate Diagnostics, Inc. | Rapid cell purification systems |
EP2693200B1 (en) * | 2011-03-29 | 2019-06-12 | Hamamatsu Photonics K.K. | Terahertz-wave spectrometer |
CN105606577B (en) | 2011-06-24 | 2019-08-13 | 贝克顿·迪金森公司 | Absorption spectrum scans flow cytometry |
TW202242379A (en) * | 2011-08-29 | 2022-11-01 | 美商安美基公司 | Methods and apparati for nondestructive detection of undissolved particles in a fluid |
KR102067367B1 (en) | 2011-09-07 | 2020-02-11 | 라피스캔 시스템스, 인코포레이티드 | X-ray inspection method that integrates manifest data with imaging/detection processing |
FR2981283B1 (en) * | 2011-10-13 | 2014-08-29 | Chambre De Commerce Et De L Ind De Paris Au Titre De Son Etablissement D Enseignement Superieur Esie | MICROFLUIDIC DEVICE FOR ANALYZING A FLUID UNDER PRESSURE. |
US8994945B2 (en) | 2011-10-27 | 2015-03-31 | Fluid Imaging Technologies, Inc. | Method of treatment analysis with particle imaging |
PL2776550T3 (en) | 2011-11-07 | 2018-05-30 | Rapid Micro Biosystems, Inc. | Cassette for sterility testing |
EP2618130A1 (en) * | 2012-01-17 | 2013-07-24 | F. Hoffmann-La Roche AG | Device for use in the detection of binding affinities |
BR112014019298A2 (en) * | 2012-02-04 | 2021-01-19 | Douglas Scientific | METHOD AND APPARATUS FOR QUICK ANALYSIS, HIGH SENSITIVITY, LOW VOLUME SAMPLES OF BIOLOGICAL MATERIALS |
MY193914A (en) | 2012-03-05 | 2022-11-01 | Oy Arctic Partners Ab | Methods and apparatuses for predicting risk of prostate cancer and prostate gland volume |
EP4060016A1 (en) | 2012-04-16 | 2022-09-21 | Rapid Micro Biosystems, Inc. | Cell culturing device |
US8879797B2 (en) | 2012-05-25 | 2014-11-04 | Fluid Imaging Technologies, Inc. | System and method for total internal reflection enhanced imaging flow cytometry |
EA030193B1 (en) * | 2012-07-27 | 2018-07-31 | Инджендер Текнолоджиз Лимитед | Method and system for microfluidic particle orientation and/or sorting |
KR101384386B1 (en) | 2012-10-25 | 2014-04-10 | 전남대학교산학협력단 | Apparatus for measuring physical properties of low permeable rocks |
US10610861B2 (en) | 2012-12-17 | 2020-04-07 | Accellix Ltd. | Systems, compositions and methods for detecting a biological condition |
EP2932266A4 (en) | 2012-12-17 | 2016-11-30 | Leukodx Ltd | Systems and methods for determining a chemical state |
US9759722B2 (en) * | 2012-12-17 | 2017-09-12 | Leukodx Ltd. | Systems and methods for determining a chemical state |
CN105324489A (en) * | 2013-03-04 | 2016-02-10 | 韦拉克斯生物医学股份有限公司 | Multi-analyte assay |
KR20150125000A (en) * | 2013-03-05 | 2015-11-06 | 에프. 호프만-라 로슈 아게 | Method and system for determining a biological response of a target to a soluble candidate sbstance |
ES2741001T3 (en) | 2013-03-13 | 2020-02-07 | Opko Diagnostics Llc | Mixing fluids in fluid systems |
US9677109B2 (en) | 2013-03-15 | 2017-06-13 | Accelerate Diagnostics, Inc. | Rapid determination of microbial growth and antimicrobial susceptibility |
CN103267854B (en) * | 2013-05-03 | 2015-08-05 | 西安交通大学 | A kind of method strengthening detection paper signal |
EP2827130A1 (en) * | 2013-07-15 | 2015-01-21 | F. Hoffmann-La Roche AG | Device for use in the detection of binding affinities |
SG10201803850YA (en) * | 2013-11-12 | 2018-06-28 | Agency Science Tech & Res | Quantitative real-time and end-point colorimetric pcr device |
EP3087370B1 (en) * | 2013-12-23 | 2022-02-16 | Siemens Healthineers Nederland B.V. | Detection apparatus for detecting particles on a surface |
US9645070B2 (en) * | 2014-06-03 | 2017-05-09 | The Regents Of The University Of California | Nanoparticle analyzer |
US10133048B2 (en) * | 2014-07-09 | 2018-11-20 | Ntp Nano Tech Projects S.R.L. | Laser optical coupling for nanoparticles detection |
KR102587637B1 (en) | 2014-12-12 | 2023-10-10 | 옵코 다이어그노스틱스, 엘엘씨 | Fluidic systems comprising an incubation channel, including fluidic systems formed by molding |
JP2018048811A (en) * | 2015-01-30 | 2018-03-29 | 京セラ株式会社 | Sensing method of detection object |
US10458990B1 (en) * | 2015-03-06 | 2019-10-29 | Scanit Technologies, Inc. | Spore state discrimination |
EP3278115A2 (en) | 2015-03-30 | 2018-02-07 | Accelerate Diagnostics, Inc. | Instrument and system for rapid microorganism identification and antimicrobial agent susceptibility testing |
US10253355B2 (en) | 2015-03-30 | 2019-04-09 | Accelerate Diagnostics, Inc. | Instrument and system for rapid microorganism identification and antimicrobial agent susceptibility testing |
USD804682S1 (en) | 2015-08-10 | 2017-12-05 | Opko Diagnostics, Llc | Multi-layered sample cassette |
EP3591439B1 (en) * | 2015-08-28 | 2021-11-17 | National University Corporation Gunma University | Charged particle radiation measuring method and charged particle radiation measuring device |
US9983115B2 (en) | 2015-09-21 | 2018-05-29 | Fluid Imaging Technologies, Inc. | System and method for monitoring particles in a fluid using ratiometric cytometry |
CN105259086B (en) * | 2015-10-29 | 2018-03-27 | 广东美的制冷设备有限公司 | The detection method and detecting system of dust concentration |
US20170160187A1 (en) * | 2015-12-08 | 2017-06-08 | Tdk Corporation | Laser Scanner Particle Counter and Imager |
EP3387447A4 (en) | 2015-12-11 | 2019-08-28 | Opko Diagnostics, LLC | Fluidic systems involving incubation samples and/or reagents |
JP6155452B1 (en) * | 2016-02-16 | 2017-07-05 | 国立大学法人電気通信大学 | Particle detection device on substrate |
EP3420563A4 (en) | 2016-02-22 | 2020-03-11 | Rapiscan Systems, Inc. | Systems and methods for detecting threats and contraband in cargo |
ITUA20161345A1 (en) * | 2016-03-04 | 2017-09-04 | Eltek Spa | SENSOR DEVICE FOR CONTAINERS OF LIQUID SUBSTANCES |
AU2017345814B2 (en) * | 2016-10-21 | 2022-07-28 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Molecular nanotags |
CN106829856A (en) * | 2016-12-14 | 2017-06-13 | 佛山旋疯纳米科技有限公司 | A kind of cluster ions beam nanoprocessing plant control unit and its control method |
JP7305611B2 (en) | 2017-03-17 | 2023-07-10 | アプトン バイオシステムズ インコーポレイテッド | Methods of sequencing and high-resolution imaging |
WO2018175039A1 (en) | 2017-03-20 | 2018-09-27 | Miller John F | Measuring electrophoretic mobility |
JP7168230B2 (en) * | 2017-06-06 | 2022-11-09 | ノースウエスタン ユニバーシティ | Trans-interfacial magnetic separation |
US11156960B2 (en) * | 2017-08-08 | 2021-10-26 | California Institute Of Technology | Focusing light inside scattering media with magnetic particle guided wavefront shaping |
CN109387460A (en) * | 2017-08-14 | 2019-02-26 | 阅美测量系统(上海)有限公司 | A kind of observation of pollution particle and test device and analysis method |
WO2019051181A1 (en) * | 2017-09-08 | 2019-03-14 | President And Fellows Of Harvard College | Nanosensor methods and apparatuses for determination of analytes |
CN109864747B (en) * | 2017-12-05 | 2023-08-25 | 心脏起搏器股份公司 | Multimode analyte sensor optoelectronic interface |
US20210341369A1 (en) * | 2018-05-18 | 2021-11-04 | President And Fellows Of Harvard College | Sample analysis with mirrors |
US11557042B2 (en) * | 2018-06-12 | 2023-01-17 | King Abdullah University Of Science And Technology | Single-camera particle tracking system and method |
JP7219390B2 (en) * | 2018-06-29 | 2023-02-08 | 澁谷工業株式会社 | Cell observation device |
CN109254022B (en) * | 2018-10-24 | 2021-07-20 | 首钢智新迁安电磁材料有限公司 | Method for measuring grain size |
CN109542186A (en) * | 2018-12-12 | 2019-03-29 | 深圳市福瑞康科技有限公司 | A kind of cabinet main box, cabinet and flash detecting device |
CN109738393B (en) * | 2019-01-10 | 2021-03-05 | 上海奥普生物医药股份有限公司 | Optical detection device and specific protein analyzer |
CN110127771B (en) * | 2019-05-31 | 2022-03-01 | 重庆科技学院 | Regulation and aggregation method of ferroferric oxide nanoparticles |
CN113049455B (en) * | 2019-12-26 | 2023-04-14 | 中核北方核燃料元件有限公司 | Cladding fuel particle and nuclear core traceability diameter auxiliary measuring device |
CN112014369B (en) * | 2020-08-25 | 2024-02-09 | 上海市皮肤病医院 | System and method for ultrasensitive digital chromatography rapid detection of analytes |
EP4271996A1 (en) * | 2020-12-31 | 2023-11-08 | 3M Innovative Properties Company | Nanopatterned films with patterned surface chemistry |
AU2021221727A1 (en) * | 2021-04-20 | 2022-11-03 | Martin Terence Cole | IMPROVEMENTS RELATED TO PARTICLE, INCLUDING SARS-CoV-2, DETECTION AND METHODS THEREFOR |
WO2022240656A1 (en) * | 2021-05-10 | 2022-11-17 | The Regents Of The University Of California | Methods of analyzing shaped particles containing cells using fluorescence activated cell sorting |
CN113340894B (en) * | 2021-05-28 | 2023-04-07 | 上海睿钰生物科技有限公司 | Detection method of non-transparent particles |
CN113552041B (en) * | 2021-06-08 | 2022-10-11 | 上海交通大学 | Exosome subtype analysis method based on single particle imaging |
US11828175B2 (en) | 2021-07-08 | 2023-11-28 | Saudi Arabian Oil Company | Systems and methods for measuring phase flow rates of a multiphase production fluid |
KR102638903B1 (en) * | 2021-12-21 | 2024-02-22 | 공주대학교 산학협력단 | Apparatus and method for vision analyzing surface fine abrasive particle of abrasive tool |
US20230194517A1 (en) * | 2021-12-21 | 2023-06-22 | Bio-Rad Laboratories, Inc. | Multiplex detection in high resolution devices through measurement of localized fluorescence ratios |
CN114295550A (en) * | 2021-12-31 | 2022-04-08 | 电子科技大学长三角研究院(湖州) | Optical flow control device based on surface lattice resonance and application thereof |
CN114152574B (en) * | 2021-12-31 | 2023-10-17 | 天津工业大学 | Portable water quality analyzer for detecting integrity of membrane assembly and detection method thereof |
CN114491387B (en) * | 2022-04-06 | 2022-07-12 | 天津美腾科技股份有限公司 | Method and device for arranging identification equipment of dry separator, electronic equipment and separation system |
CN116448637B (en) * | 2023-06-14 | 2023-09-08 | 北京建工环境修复股份有限公司 | Method for detecting nano plastic by modified gold particle marked dark field microscopic imaging |
Family Cites Families (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3975084A (en) | 1973-09-27 | 1976-08-17 | Block Engineering, Inc. | Particle detecting system |
US3939350A (en) * | 1974-04-29 | 1976-02-17 | Board Of Trustees Of The Leland Stanford Junior University | Fluorescent immunoassay employing total reflection for activation |
US4210384A (en) * | 1976-09-11 | 1980-07-01 | Carl Zeiss-Stiftung | Inverted-design optical microscope |
NL7807532A (en) | 1978-07-13 | 1980-01-15 | Akzo Nv | METAL IMMUNO TEST. |
US4245031A (en) * | 1979-09-18 | 1981-01-13 | E. I. Du Pont De Nemours And Company | Photopolymerizable compositions based on salt-forming polymers and polyhydroxy polyethers |
US4420558A (en) | 1981-02-12 | 1983-12-13 | Janssen Pharmaceutica N.V. | Bright field light microscopic method of enumerating and characterizing subtypes of white blood cells and their precursors |
GB2095258B (en) | 1981-03-19 | 1984-09-05 | Janssen Pharmaceutica Nv | A bright field light microscopic method of localizing tissue antigens |
US4480042A (en) | 1981-10-28 | 1984-10-30 | E. I. Du Pont De Nemours And Company | Covalently bonded high refractive index particle reagents and their use in light scattering immunoassays |
US4597944A (en) * | 1983-10-18 | 1986-07-01 | Cottingham Hugh V | Agglutination reagent detection system |
JPS60149130A (en) * | 1984-01-17 | 1985-08-06 | Hitachi Ltd | Method for pattern detection |
US4624923A (en) * | 1984-06-08 | 1986-11-25 | Yeda Research And Development Company Limited | Metal-coated polyaldehyde microspheres |
US4752567A (en) | 1984-06-21 | 1988-06-21 | Janssen Pharmaceutica N.V. | Method of visualizing individual submicroscopic metal particles |
US4647544A (en) * | 1984-06-25 | 1987-03-03 | Nicoli David F | Immunoassay using optical interference detection |
CA1291031C (en) * | 1985-12-23 | 1991-10-22 | Nikolaas C.J. De Jaeger | Method for the detection of specific binding agents and their correspondingbindable substances |
US5137827A (en) * | 1986-03-25 | 1992-08-11 | Midwest Research Technologies, Inc. | Diagnostic element for electrical detection of a binding reaction |
US4877647A (en) * | 1986-04-17 | 1989-10-31 | Kansas State University Research Foundation | Method of coating substrates with solvated clusters of metal particles |
US4929400A (en) * | 1986-04-28 | 1990-05-29 | California Institute Of Technology | Production of monodisperse, polymeric microspheres |
US4851329A (en) | 1986-06-06 | 1989-07-25 | Massachusetts Institute Of Technology | Immunoassay employing optical pulse particle size analysis |
US5514602A (en) | 1986-06-09 | 1996-05-07 | Ortho Diagnostic Systems, Inc. | Method of producing a metal sol reagent containing colloidal metal particles |
US5017009A (en) * | 1986-06-26 | 1991-05-21 | Ortho Diagnostic Systems, Inc. | Scattered total internal reflectance immunoassay system |
US4876208A (en) * | 1987-01-30 | 1989-10-24 | Yellowstone Diagnostics Corporation | Diffraction immunoassay apparatus and method |
DE3789547T2 (en) * | 1987-02-13 | 1994-07-14 | Toray Industries | Anti-reflective optical object and process for its production. |
US5202231A (en) | 1987-04-01 | 1993-04-13 | Drmanac Radoje T | Method of sequencing of genomes by hybridization of oligonucleotide probes |
US4806583A (en) * | 1987-06-19 | 1989-02-21 | Battaglia Charles R | Antiglare coating |
GB8803000D0 (en) | 1988-02-10 | 1988-03-09 | Ekins Roger Philip | Determination of ambient concentrations of several analytes |
US4979821A (en) * | 1988-01-27 | 1990-12-25 | Ortho Diagnostic Systems Inc. | Cuvette for receiving liquid sample |
NO164622C (en) | 1988-05-11 | 1990-10-24 | Tore Lindmo | BINAER IMMUNOMETRIC PARTICLE-BASED METHOD FOR MEASURING SPECIFIC SERUM ANTIGENS USING LIQUID FLOW MICROPHOTOMETRY AND A PREPARED TARGET SET UP THEREOF. |
DE3826055A1 (en) * | 1988-07-30 | 1990-02-01 | Boehringer Mannheim Gmbh | REAGENT-RELEASED TRAEGERMATRIX WITH REAGENT |
US5079172A (en) | 1988-11-04 | 1992-01-07 | Board Of Trustees Operating Michigan State University | Method for detecting the presence of antibodies using gold-labeled antibodies and test kit |
US5100805A (en) * | 1989-01-26 | 1992-03-31 | Seradyn, Inc. | Quantitative immunoassay system and method for agglutination assays |
US6309822B1 (en) | 1989-06-07 | 2001-10-30 | Affymetrix, Inc. | Method for comparing copy number of nucleic acid sequences |
US5145748A (en) * | 1989-06-20 | 1992-09-08 | W.R. Grace & Co. -Conn. | Waterproofing system for water-penetrable construction surfaces |
US5376556A (en) * | 1989-10-27 | 1994-12-27 | Abbott Laboratories | Surface-enhanced Raman spectroscopy immunoassay |
JP2899360B2 (en) | 1990-05-21 | 1999-06-02 | 興和株式会社 | Method and apparatus for measuring particles in fluid |
US5350697A (en) * | 1990-08-28 | 1994-09-27 | Akzo N.V. | Scattered light detection apparatus |
US5294369A (en) | 1990-12-05 | 1994-03-15 | Akzo N.V. | Ligand gold bonding |
US5784162A (en) * | 1993-08-18 | 1998-07-21 | Applied Spectral Imaging Ltd. | Spectral bio-imaging methods for biological research, medical diagnostics and therapy |
JP3115641B2 (en) | 1991-04-24 | 2000-12-11 | シスメックス株式会社 | Particle counting method |
US5286452A (en) | 1991-05-20 | 1994-02-15 | Sienna Biotech, Inc. | Simultaneous multiple assays |
JP2523227Y2 (en) | 1991-07-30 | 1997-01-22 | 株式会社堀場製作所 | Foreign matter inspection device |
US5151956A (en) | 1991-12-20 | 1992-09-29 | The United Staes Of America As Represented By The Secretary Of The Army | Waveguide polarizer using localized surface plasmons |
US5248772A (en) * | 1992-01-29 | 1993-09-28 | Coulter Corporation | Formation of colloidal metal dispersions using aminodextrans as reductants and protective agents |
US5305073A (en) | 1992-02-12 | 1994-04-19 | Precision Detectors, Inc. | Methods and apparatus for molecular characterization |
US5518887A (en) * | 1992-03-30 | 1996-05-21 | Abbott Laboratories | Immunoassays empolying generic anti-hapten antibodies and materials for use therein |
DE4404128A1 (en) * | 1993-02-19 | 1994-08-25 | Gao Ges Automation Org | Security document and method for its manufacture |
US5350911A (en) * | 1993-04-09 | 1994-09-27 | Hughes Aircraft Company | Wavefront error estimation derived from observation of arbitrary unknown extended scenes |
DE4414166C1 (en) * | 1994-04-22 | 1995-12-07 | Lorenz Mesgeraetebau | Method and device for measuring light scattering on particles |
US5734498A (en) * | 1994-05-09 | 1998-03-31 | The Regents Of The University Of California | Illuminator elements for conventional light microscopes |
US5807522A (en) * | 1994-06-17 | 1998-09-15 | The Board Of Trustees Of The Leland Stanford Junior University | Methods for fabricating microarrays of biological samples |
US5728590A (en) * | 1994-07-29 | 1998-03-17 | Nanoprobes, Inc. | Small organometallic probes |
US5498875A (en) * | 1994-08-17 | 1996-03-12 | Beckman Instruments, Inc. | Signal processing for chemical analysis of samples |
US5599668A (en) | 1994-09-22 | 1997-02-04 | Abbott Laboratories | Light scattering optical waveguide method for detecting specific binding events |
US6159748A (en) * | 1995-03-13 | 2000-12-12 | Affinitech, Ltd | Evaluation of autoimmune diseases using a multiple parameter latex bead suspension and flow cytometry |
JP3284056B2 (en) * | 1995-09-12 | 2002-05-20 | 株式会社東芝 | Substrate processing apparatus and pattern forming method |
US5981180A (en) * | 1995-10-11 | 1999-11-09 | Luminex Corporation | Multiplexed analysis of clinical specimens apparatus and methods |
WO1997015819A1 (en) * | 1995-10-25 | 1997-05-01 | University Of Washington | Surface plasmon resonance light pipe sensor |
US5851777A (en) * | 1996-02-05 | 1998-12-22 | Dade Behring Inc. | Homogeneous sol-sol assay |
US6586193B2 (en) * | 1996-04-25 | 2003-07-01 | Genicon Sciences Corporation | Analyte assay using particulate labels |
IL126544A (en) * | 1996-04-25 | 2004-08-31 | Genicon Sciences Inc | Analyte assay using scattered-light detectable particles |
US5856018A (en) * | 1996-06-17 | 1999-01-05 | Yazaki Corporation | Plastic articles having multi-layer antireflection coatings, and sol-gel process for depositing such coatings |
JP2002514046A (en) * | 1996-07-08 | 2002-05-14 | バースタイン テクノロジーズ,インコーポレイティド | Devices and methods for cleavable signaling factors |
US6165798A (en) * | 1996-10-10 | 2000-12-26 | University Of British Columbia | Optical quantification of analytes in membranes |
JPH10206603A (en) * | 1997-01-20 | 1998-08-07 | Dainippon Printing Co Ltd | Reflection preventive film and manufacture thereof |
US6122042A (en) * | 1997-02-07 | 2000-09-19 | Wunderman; Irwin | Devices and methods for optically identifying characteristics of material objects |
WO1998037417A1 (en) | 1997-02-20 | 1998-08-27 | The Regents Of The University Of California | Plasmon resonant particles, methods and apparatus |
US6294327B1 (en) | 1997-09-08 | 2001-09-25 | Affymetrix, Inc. | Apparatus and method for detecting samples labeled with material having strong light scattering properties, using reflection mode light and diffuse scattering |
JP3507319B2 (en) * | 1997-12-08 | 2004-03-15 | キヤノン株式会社 | Optical property measurement device |
US6087102A (en) * | 1998-01-07 | 2000-07-11 | Clontech Laboratories, Inc. | Polymeric arrays and methods for their use in binding assays |
US6311275B1 (en) * | 1998-08-03 | 2001-10-30 | Cisco Technology, Inc. | Method for providing single step log-on access to a differentiated computer network |
US6171793B1 (en) * | 1999-04-19 | 2001-01-09 | Affymetrix, Inc. | Method for scanning gene probe array to produce data having dynamic range that exceeds that of scanner |
US6627923B1 (en) * | 1999-07-12 | 2003-09-30 | Massachusetts Institute Of Technology | Resonant microcavities |
KR20010108656A (en) * | 2000-05-30 | 2001-12-08 | 윤종용 | Method of programing flash memory |
WO2002068932A2 (en) * | 2001-02-23 | 2002-09-06 | Genicon Sciences Corporation | Methods for providing extended dynamic range in analyte assays |
US6714299B2 (en) * | 2001-07-13 | 2004-03-30 | Genicon Sciences Corporation | Use of light scattering particles in design, manufacture, and quality control of small volume instruments, devices, and processes |
US7555173B2 (en) * | 2003-04-09 | 2009-06-30 | Cornell Research Foundation, Inc. | Electro-optic modulator on rib waveguide |
-
1997
- 1997-10-17 US US08/953,713 patent/US6586193B2/en not_active Expired - Lifetime
-
1998
- 1998-10-16 JP JP2000517107A patent/JP4247770B2/en not_active Expired - Fee Related
- 1998-10-16 AU AU12943/99A patent/AU1294399A/en not_active Abandoned
- 1998-10-16 RU RU2000112095/13A patent/RU2217498C2/en not_active IP Right Cessation
- 1998-10-16 CA CA2719432A patent/CA2719432A1/en not_active Abandoned
- 1998-10-16 CN CNB988122790A patent/CN100379876C/en not_active Expired - Fee Related
- 1998-10-16 IL IL13569698A patent/IL135696A/en not_active IP Right Cessation
- 1998-10-16 CA CA2307280A patent/CA2307280C/en not_active Expired - Fee Related
- 1998-10-16 BR BR9814821-4A patent/BR9814821A/en not_active Application Discontinuation
- 1998-10-16 WO PCT/US1998/023160 patent/WO1999020789A1/en active Application Filing
- 1998-10-16 EP EP98956415A patent/EP1023456A1/en not_active Withdrawn
-
2001
- 2001-07-12 HK HK01104872A patent/HK1034291A1/en not_active IP Right Cessation
- 2001-08-16 US US09/932,128 patent/US20030157731A1/en not_active Abandoned
- 2001-08-16 US US09/931,729 patent/US20020045276A1/en not_active Abandoned
-
2002
- 2002-10-30 US US10/283,950 patent/US20030207328A1/en not_active Abandoned
-
2004
- 2004-09-22 US US10/947,636 patent/US7255995B2/en not_active Expired - Fee Related
-
2006
- 2006-12-28 US US11/617,446 patent/US20070184471A1/en not_active Abandoned
-
2008
- 2008-06-23 US US12/144,439 patent/US8227260B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109957503A (en) * | 2017-12-14 | 2019-07-02 | 长光华大基因测序设备(长春)有限公司 | A kind of processing chip and its application for high-throughput gene sequencing equipment |
CN109957503B (en) * | 2017-12-14 | 2022-05-31 | 长春长光华大智造测序设备有限公司 | Process chip for high-throughput gene sequencing equipment and application thereof |
Also Published As
Publication number | Publication date |
---|---|
AU1294399A (en) | 1999-05-10 |
EP1023456A1 (en) | 2000-08-02 |
WO1999020789A1 (en) | 1999-04-29 |
CN100379876C (en) | 2008-04-09 |
US20050112784A1 (en) | 2005-05-26 |
US20020045276A1 (en) | 2002-04-18 |
JP2001520398A (en) | 2001-10-30 |
HK1034291A1 (en) | 2001-10-19 |
US20020028519A1 (en) | 2002-03-07 |
CA2307280C (en) | 2010-12-14 |
US20030157731A1 (en) | 2003-08-21 |
IL135696A0 (en) | 2001-05-20 |
RU2217498C2 (en) | 2003-11-27 |
US20030207328A1 (en) | 2003-11-06 |
BR9814821A (en) | 2001-11-20 |
US20070184471A1 (en) | 2007-08-09 |
CN1282378A (en) | 2001-01-31 |
CA2719432A1 (en) | 1999-04-29 |
US8227260B2 (en) | 2012-07-24 |
US20090004757A1 (en) | 2009-01-01 |
IL135696A (en) | 2004-03-28 |
US7255995B2 (en) | 2007-08-14 |
US6586193B2 (en) | 2003-07-01 |
JP4247770B2 (en) | 2009-04-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2307280A1 (en) | Analyte assay using particulate labels | |
US10670592B2 (en) | Detection of analytes using metal nanoparticle probes and dynamic light scattering | |
US6492125B2 (en) | Method to assess library X library interactions | |
JP4318859B2 (en) | Combined assay method | |
US6713271B1 (en) | Systems and methods for performing magnetic chromatography assays | |
JP4997222B2 (en) | Multifunctional and configurable assay | |
US9389223B2 (en) | Pharmacodynamic assays | |
US6730521B1 (en) | Chemical and biochemical assay method and apparatus | |
US20080293590A1 (en) | Multianalyte assay method | |
Nolan et al. | Flow cytometry: a versatile tool for all phases of drug discovery | |
JPH0754324B2 (en) | Test agent for measuring antigen and / or antibody in liquid sample | |
EP1448990B1 (en) | Particle-based ligand assay with extended dynamic range | |
EP1110090B1 (en) | Multihued labels | |
JP2005510706A5 (en) | ||
US6756014B2 (en) | Biochemical sensor and biochemical testing system using the same | |
Wang et al. | Quantitative detection of malachite green in sediment by a time-resolved immunofluorescence method combined with a portable 3D printing equipment platform | |
CA1197186A (en) | Method of enumerating serologically selected cell populations | |
Chuang et al. | Rapid point-of-care multiplex immunodetection using two-dimensional microarray technology | |
JPS61290362A (en) | Measurement of fine particle size | |
NO842501L (en) | PROCEDURE AND METHOD FOR DETECTING ANTIGENS AND / OR ANTIBODIES. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |