Unit

UNIT 6.13 Immunophenotyping Using a Laser Scanning Cytometer

  1. Attila Tárnok,
  2. Andreas O.H. Gerstner

Published Online: 1 FEB 2003

DOI: 10.1002/0471142956.cy0613s23

Current Protocols in Cytometry

Current Protocols in Cytometry

How to Cite

Tárnok, A. and Gerstner, A. O. 2003. Immunophenotyping Using a Laser Scanning Cytometer. Current Protocols in Cytometry. 23:6.13:6.13.1–6.13.15.

Author Information

  1. University of Leipzig, Leipzig, Germany

Publication History

  1. Published Online: 1 FEB 2003
  2. Published Print: JAN 2003

Abstract

Three- and four-color immunophenotyping is routine in traditional flow cytometry, as is measurement of cell proliferation, but there are drawbacks. The techniques cannot analyze cell morphology or permit restaining of cells of interest. This unit describes a slide-based method of immunophenotyping using a laser scanning cytometer. In general, many assays originally developed for flow can be adapted to LSC. Although the speed of analysis is comparatively slow, LSC has the advantage that cells are not lost. Considerable additional information can be obtained by morphological examination and/or by further staining because specimens can be repeatedly analyzed and archived. The method has potential to become a powerful tool in clinical diagnosis.