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PMID: 6883722 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Determination of Gaucher's disease phenotypes with monoclonal antibody.

Clinica chimica acta; international journal of clinical chemistry ·Vol. 131 ·No. 3 ·1983-07-15 ·Pages 283-7

Ginns EI, Tegelaers FP, Barneveld R, Galjaard H, Reuser AJ, Brady RO, Tager JM, Barranger JA

Abstract

Discrimination between the three clinical subtypes of Gaucher's disease based on the molecular forms of beta-glucocerebrosidase detected by monoclonal antibody is described. In normal fibroblast extracts, cross-reacting material (CRM) to human placental glucocerebrosidase is detected at Mr approximately equal to 63 000, 61 000 and 56 000. In Type 1 Gaucher's disease, the major fibroblast CRM has a Mr approximately equal to 56 000,, with less CRM seen at 61 000 and 56 000. Type 3 fibroblast extracts have a single CRM form at Mr approximately equal to 63 000. No CRM is found in Type 2 Gaucher's disease fibroblasts with monoclonal antiglucocerebrosidase antibody 8E4.

MeSH Terms
Antibodies, Monoclonal Fibroblasts/enzymology Gaucher Disease/diagnosis,genetics Glucosidases/isolation & purification Glucosylceramidase/immunology,isolation & purification Humans Immunochemistry Phenotype
Chemicals
Antibodies, Monoclonal Glucosidases Glucosylceramidase
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Ginns E I
Tegelaers F P
Barneveld R
Galjaard H
Reuser A J
Brady R O
Tager J M
Barranger J A
Article Info
Journal
Clinica chimica acta; international journal of clinical chemistry
Abbr.
Clin Chim Acta
ISSN
0009-8981
Published
1983-07-15
Pages
283-7
Language
English
Region
Netherlands
NLM ID
1302422
Subset
IM
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