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PMID: 3131277 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

C4 allotyping on plasma or serum: application to routine laboratories.

Human immunology ·Vol. 21 ·No. 3 ·1988-03-00 ·Pages 165-71

Zhang WJ, Kay PH, Cobain TJ, Dawkins RL

Abstract

Allotypes of the fourth component of complement (C4) can be detected by electrophoresis and immunofixation after treatment of EDTA plasma with neuraminidase (NAse). We have assessed the value of additional treatment with carboxypeptidase B (CPseB). Following treatment with CPseB + NAse, each allele is resolved into a single band, permitting clear definition of overlapping bands seen following treatment with NAse alone. More importantly, C4 allotypes can be determined using stored heparinized plasma or serum. Most C4 null alleles can be assigned without requiring family studies. The approach described is suitable for routine use by tissue typing laboratories.

MeSH Terms
Alleles Carboxypeptidase B Carboxypeptidases/metabolism Complement C4/genetics,immunology Edetic Acid Electrophoresis, Polyacrylamide Gel Heparin In Vitro Techniques Isoantigens/immunology Neuraminidase/metabolism Phenotype
Chemicals
Complement C4 Isoantigens Heparin Edetic Acid Neuraminidase Carboxypeptidases Carboxypeptidase B
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Zhang W J
Department of Clinical Immunology, Royal Perth Hospital, Queen Elizabeth II Medical Centre, Western Australia.
Kay P H
Cobain T J
Dawkins R L
Article Info
Journal
Human immunology
Abbr.
Hum Immunol
ISSN
0198-8859
Published
1988-03-00
Pages
165-71
Language
English
Region
United States
NLM ID
8010936
Subset
IM
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