Results 311 to 320 of about 1,097,210 (332)
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Medical Physics, 1980
A brief review of flow cytometry is presented. Emphasis is on the construction of relatively simple instruments and on their application to problems in medical physics. Among these are the problems of measuring the biological parameters that determine the response of tumors to therapy and of measuring the biological damage in people exposed to ionizing
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A brief review of flow cytometry is presented. Emphasis is on the construction of relatively simple instruments and on their application to problems in medical physics. Among these are the problems of measuring the biological parameters that determine the response of tumors to therapy and of measuring the biological damage in people exposed to ionizing
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Current Protocols in Cytometry, 2001
AbstractAlthough flow cytometry has the powerful ability to rapidly screen large collections of cells, the technology has yet to be efficiently applied to large‐scale screening operations involving multiple discrete suspensions. High‐throughput flow cytometry would be beneficial to many areas of biological investigation, such as modern drug discovery ...
B S, Edwards, L A, Sklar
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AbstractAlthough flow cytometry has the powerful ability to rapidly screen large collections of cells, the technology has yet to be efficiently applied to large‐scale screening operations involving multiple discrete suspensions. High‐throughput flow cytometry would be beneficial to many areas of biological investigation, such as modern drug discovery ...
B S, Edwards, L A, Sklar
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Differential Mobility Cytometry
Analytical Chemistry, 2009A new cell analysis method, differential mobility cytometry (DMC), was developed to monitor cells spatially and temporally or to separate cells based on affinity interactions. DMC combines an oscillation system with open-tubular capillary cell affinity chromatography (OT-CAC), although any separation volume (capillaries, channels, etc.) can be used ...
Kelong, Wang +5 more
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Current Protocols in Cytometry, 2004
AbstractThere are many tasks to which flow cytometers are unsuited, e.g., measurement of attached cells, repeated measurements of a single cell over time, and localization of probes in or on cells. Devices such as confocal microscopes and microscope‐based imaging systems allow high‐resolution analysis and provide flexibility, but typically have low ...
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AbstractThere are many tasks to which flow cytometers are unsuited, e.g., measurement of attached cells, repeated measurements of a single cell over time, and localization of probes in or on cells. Devices such as confocal microscopes and microscope‐based imaging systems allow high‐resolution analysis and provide flexibility, but typically have low ...
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2010
Cell-based arrays offer powerful tools for genomics/proteomics and drug discovery, and are widely applicable for most cell lines. However, it is challenging to apply cell-based arrays for in vitro diagnosis due to limited amount of patient samples. Here, we utilized and demonstrated microfluidic image cytometry (MIC), capable of quantitative, single ...
Ken-ichiro, Kamei +3 more
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Cell-based arrays offer powerful tools for genomics/proteomics and drug discovery, and are widely applicable for most cell lines. However, it is challenging to apply cell-based arrays for in vitro diagnosis due to limited amount of patient samples. Here, we utilized and demonstrated microfluidic image cytometry (MIC), capable of quantitative, single ...
Ken-ichiro, Kamei +3 more
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2004
Cytokine flow cytometry (CFC) is a general term that applies to flow cytometric analysis of cells using anticytokine antibodies as markers of activation. The most common version of this technique is the intracellular staining of cytokines in cells that have been fixed and permeabilized after short-term in vitro activation.
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Cytokine flow cytometry (CFC) is a general term that applies to flow cytometric analysis of cells using anticytokine antibodies as markers of activation. The most common version of this technique is the intracellular staining of cytokines in cells that have been fixed and permeabilized after short-term in vitro activation.
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Quantitative Fluorescence Cytometry
2003The phenotypes useful in distinguishing normal and neoplastic leukocytes are often identified by fluorescence staining reactions detected on flow cytometers. These reactions were originally observed by fluorescence microscopy, and cells were classified by human observers as simply negative or positive, with the positive cells sometimes distinguished as
R F, Vogt +4 more
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