Unit

UNIT 7.1 Isolation of Whole Mononuclear Cells from Peripheral Blood and Cord Blood

  1. Marjorie E. Kanof1,
  2. Phillip D. Smith2,
  3. Heddy Zola3

Published Online: 1 MAY 2001

DOI: 10.1002/0471142735.im0701s19

Current Protocols in Immunology

Current Protocols in Immunology

How to Cite

Kanof, M. E., Smith, P. D. and Zola, H. 2001. Isolation of Whole Mononuclear Cells from Peripheral Blood and Cord Blood. Current Protocols in Immunology. 19:I:7.1:7.1.1–7.1.7.

Author Information

  1. 1

    Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts

  2. 2

    National Institute of Dental Research/NIH, Bethesda, Maryland

  3. 3

    Child Health Research Institue Inc., North Adelaide, Australia

Publication History

  1. Published Online: 1 MAY 2001
  2. Published Print: SEP 1996

This is not the most recent version of the article. View current version (1 APR 2009)

Abstract

Peripheral blood is the primary source of lymphoid cells for investigations of the human immune system. Its use is facilitated by the Ficoll-Hypaque density gradient centrifugation method described here. It is a simple and rapid method of purifying peripheral blood mononuclear cells (PBMC) that takes advantage of the density differences between mononuclear cells and other elements found in the blood sample. The mononuclear cell sample can be purified from monocytes by adherence or by exposure to L-leucine methyl ester; methods are described for both procedures. Cord blood and peripheral blood from infants contain immature cells, including nucleated red cells, that can result in significant contamination of the mononuclear cell layer, and removal of these cells requires additional steps that are described. The isolation procedures presented here can also be applied to cell populations derived from tissues.