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PMID: 11309812 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

High throughput flow cytometry.

Cytometry ·Vol. 44 ·No. 1 ·2001-05-01 ·Pages 83-90

Kuckuck FW, Edwards BS, Sklar LA

Abstract

Conventional flow cytometry does not allow the rapid analysis of multiple samples. This has limited its uses in drug discovery, for which the standard for throughput is 100,000 samples per day. We describe a simple method in which commercial peristaltic tubing is connected from a commercial autosampler to a flow cytometer. The samples are delivered via a peristaltic pump from source wells in a multiwell plate. The samples are separated by air bubbles. Throughput rates approach the limit of the autosampler (up to 100 wells per minute). Using optimal tubing and flow rates, particles remain within appropriate light scatter and fluorescence gates. The carryover between wells is typically less than 5% without and 1% with a wash step. The volumes of sample delivered are in the microliter scale. The approach has been validated with instruments from three manufacturers. Flow cytometry has potential throughput of 100,000 samples or more per day starting with the method described. The method is currently best suited to end-point assays. However, combined with high-speed sorting and single- cell assays, the number of assays could approach 1 billion per day.

MeSH Terms
Flow Cytometry/instrumentation,methods Humans Sensitivity and Specificity Time Factors U937 Cells
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kuckuck F W
Cytometry, Cancer Research and Treatment Center, University of New Mexico Health Sciences Center, Albuquerque, New Mexico.
Edwards B S
Sklar L A
Article Info
Journal
Cytometry
Abbr.
Cytometry
ISSN
0196-4763
Published
2001-05-01
Pages
83-90
Language
English
Region
United States
NLM ID
8102328
Subset
IM
Grants
NIGMS NIH HHS · GM 60799 · United States
External Links
PubMed source
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