Have a personal or library account? Click to login
En(a–) phenotype in a Japanese blood donor Cover

En(a–) phenotype in a Japanese blood donor

Paid access
|Jun 2020

Abstract

The first Japanese En(a–) individual (T.N.) was found by screening red cells from 250,000 Japanese blood donors with monoclonal anti-Ena. His serum contained no atypical antibodies and his partial red cell phenotype was M–N–S+s–, although a trypsinresistant N antigen was detected. His red cells were En(a–) and Wr(b–), as determined by various human and mouse monoclonal antibodies. The absence of glycophorin A (GPA) and the presence of apparently normal glycophorin B (GPB) were demonstrated by immunoblotting with antibodies to the extracellular and cytoplasmic domain of GPA and to epitopes common to GPA and GPB. Sialic acid levels of T.N.’s intact red cells were substantially lower than those of control MN cells. Serologic tests suggested that both of T.N.’s parents were heterozygous for a recessive GPA deficiency gene. Immunohematology 1993;9:105.

DOI: https://doi.org/10.21307/immunohematology-2019-969 | Journal eISSN: 1930-3955 | Journal ISSN: 0894-203X
Language: English
Page range: 105 - 108
Published on: Jun 12, 2020
Published by: American National Red Cross
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2020 Y. Okubo, T. Seno, H. Yamaguchi, Y. Miyata, C.A. Green, G.L. Daniels, published by American National Red Cross
This work is licensed under the Creative Commons License.