Laser scanning cytometry: principles and applications.
Methods in molecular biology (Clifton, N.J.), ISSN: 1064-3745, Vol: 319, Page: 165-192
2006
- 67Citations
- 31Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations67
- Citation Indexes67
- 67
- CrossRef48
- Captures31
- Readers31
- 28
Book Chapter Description
The laser scanning cytometer (LSC) is the microscope-based cytofluorometer that offers a plethora of analytical capabilities. Multilaser-excited fluorescence emitted from individual cells is measured at several wavelength ranges, rapidly (up to 5000 cells/min), with high sensitivity and accuracy. The following applications of LSC are reviewed: (1) identification of cells that differ in degree of chromatin condensation (e.g., mitotic or apoptotic cells or lymphocytes vs granulocytes vs monocytes); (2) detection of translocation between cytoplasm vs nucleus or nucleoplasm vs nucleolus of regulatory molecules such as NF-kappaB, p53, or Bax; (3) semiautomatic scoring of micronuclei in mutagenicity assays; (4) analysis of fluorescence in situ hybridization; (5) enumeration and morphometry of nucleoli; (6) analysis of phenotype of progeny of individual cells in clonogenicity assay; (7) cell immunophenotyping; (8) visual examination, imaging, or sequential analysis of the cells measured earlier upon their relocation, using different probes; (9) in situ enzyme kinetics and other time-resolved processes; (10) analysis of tissue section architecture; (11) application for hypocellular samples (needle aspirate, spinal fluid, etc.); (12) other clinical applications. Advantages and limitations of LSC are discussed and compared with flow cytometry.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=33747421048&origin=inward; http://dx.doi.org/10.1007/978-1-59259-993-6_8; http://www.ncbi.nlm.nih.gov/pubmed/16719355; http://link.springer.com/10.1007/978-1-59259-993-6_8; https://dx.doi.org/10.1007/978-1-59259-993-6_8; https://link.springer.com/protocol/10.1007/978-1-59259-993-6_8; http://www.springerlink.com/index/10.1007/978-1-59259-993-6_8; http://www.springerlink.com/index/pdf/10.1007/978-1-59259-993-6_8
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