Cloning and sequencing of cDNAs encoding the human sperm protein, Sp17
被引:47
作者:
Lea, IA
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机构:Dept. of Cell Biology and Anatomy, Univ. of N. Carolina at Chapel Hill, CB #7090, Chapel Hill
Lea, IA
Richardson, RT
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h-index: 0
机构:Dept. of Cell Biology and Anatomy, Univ. of N. Carolina at Chapel Hill, CB #7090, Chapel Hill
Richardson, RT
Widgren, EE
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机构:Dept. of Cell Biology and Anatomy, Univ. of N. Carolina at Chapel Hill, CB #7090, Chapel Hill
Widgren, EE
ORand, MG
论文数: 0引用数: 0
h-index: 0
机构:Dept. of Cell Biology and Anatomy, Univ. of N. Carolina at Chapel Hill, CB #7090, Chapel Hill
ORand, MG
机构:
[1] Dept. of Cell Biology and Anatomy, Univ. of N. Carolina at Chapel Hill, CB #7090, Chapel Hill
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
|
1996年
/
1307卷
/
03期
关键词:
cDNA cloning;
spermatozoon;
(human);
D O I:
10.1016/0167-4781(96)00077-2
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
In the present study we have cloned and sequenced two testis-specific cDNAs (1.3 kb and 1.6 kb) encoding a human sperm protein, designated HSp17. Each cDNA gave rise to identical protein sequences and differed only in the 5' untranslated region. The predicted amino-acid sequence revealed a protein of 17.5 kDa which exhibited a high degree of homology with both rabbit and mouse Sp17. Analysis of native and recombinant Sp17 by SDS-PAGE has shown the apparent molecular weight of the protein to be 24.5 kDa.