4.5 Article Book Chapter

Chemical Cytometry: Fluorescence-Based Single-Cell Analysis

期刊

ANNUAL REVIEW OF ANALYTICAL CHEMISTRY
卷 1, 期 -, 页码 165-190

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev.anchem.1.031207.113104

关键词

fluorescence; capillary electrophoresis; single-cell analysis; cytometry

资金

  1. National Institutes of Helath [R01NS061767-01, R01GM071666, R33CA122900, P50HG002360]
  2. NATIONAL CANCER INSTITUTE [R33CA122900] Funding Source: NIH RePORTER
  3. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [P50HG002360] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM071666] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS061767] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Cytometry deals with the analysis of the composition of single cells. Flow and image cytometry employ, antibody-based stains to characterize a handful of components in single cells. Chemical cytometry in contrast, employs a suite of powerful analytical tools to characterize a large number of components. Tools have been developed to characterize nucleic acids, proteins, and metabolites in single cells. Whereas nucleic acid analysis employs powerful polymerase chain reaction-based amplification techniques, protein and metabolite analysis tends to employ capillary electrophoresis separation and ultrasensitive laser-induced fluorescence detection. It is now possible to detect yoctomole amounts of many analytes in single cells.

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