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糖蛋白缺乏个体的人类红细胞膜血型糖蛋白A和血型糖蛋白B基因研究。

Studies on human red-cell membrane glycophorin A and glycophorin B genes in glycophorin-deficient individuals.

作者信息

Tate C G, Tanner M J, Judson P A, Anstee D J

机构信息

Department of Biochemistry, School of Medical Sciences, University of Bristol, U.K.

出版信息

Biochem J. 1989 Nov 1;263(3):993-6. doi: 10.1042/bj2630993.

Abstract
  1. Genomic DNA derived from individuals who lack glycophorin A (GPA), glycophorin B (GPB) or both of these proteins was subjected to Southern-blot analysis using GPA and GPB cDNA probes. 2. Bands on the Southern blots were assigned to the GPA gene, GPB gene or to a putative pseudogene. 3. Genomic DNA derived from an individual of the Mk phenotype was shown to have deletions in the GPA and GPB genes. The simplest model for the results obtained is that a single deletion spans the GPA and GPB genes in the individual studied.
摘要
  1. 从缺乏血型糖蛋白A(GPA)、血型糖蛋白B(GPB)或这两种蛋白的个体中提取的基因组DNA,使用GPA和GPB cDNA探针进行Southern印迹分析。2. Southern印迹上的条带被归为GPA基因、GPB基因或一个假定的假基因。3. 来自Mk血型个体的基因组DNA显示在GPA和GPB基因中有缺失。所得结果的最简单模型是,在被研究个体中,一个单一的缺失跨越了GPA和GPB基因。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e801/1133532/6fcfaae64a8c/biochemj00196-0361-a.jpg

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