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货号: YP-Ab-12397
促销价:

产品介绍

反应种属
Human;Rat;Mouse;
应用范围
WB
抗体类型
多克隆抗体
基因名称(Gene Name)
DAZ1 DAZ SPGY
蛋白名称
DAZ1
分子量(DA)
免疫原
Synthesized peptide derived from human DAZ1 AA range: 547-597
特异性
This antibody detects endogenous levels of DAZ1 at Human
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源
Polyclonal, Rabbit,IgG
稀释比例
WB 1:500-2000
纯化工艺
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
浓度
1 mg/ml
储存
-20°C/1 year
其他名称
背景
This gene is a member of the DAZ gene family and is a candidate for the human Y-chromosomal azoospermia factor (AZF). Its expression is restricted to premeiotic germ cells, particularly in spermatogonia. It encodes an RNA-binding protein that is important for spermatogenesis. Four copies of this gene are found on chromosome Y within palindromic duplications; one pair of genes is part of the P2 palindrome and the second pair is part of the P1 palindrome. Each gene contains a 2.4 kb repeat including a 72-bp exon, called the DAZ repeat; the number of DAZ repeats is variable and there are several variations in the sequence of the DAZ repeat. Each copy of the gene also contains a 10.8 kb region that may be amplified; this region includes five exons that encode an RNA recognition motif (RRM) domain. This gene contains three copies of the 10.8 kb repeat. However, no transcripts containing three copies of the RRM domain have been described; thus the RefSeq for this gene contains only two RRM domains. [provided by RefSeq, Jul 2008],
功能
caution:DAZ4 is the only DAZ gene whose expression has not been clearly demonstrated. PubMed:10936047 could not exclude the possibility that the transcript they isolated derives from DAZ1.,disease:AZFc deletions in the Yq11.23 region, including the DAZ genes, are a cause of azoospermia or oligospermia. They lead to male infertility due to impaired spermatogenesis and are found 2-10% of azoospermic or severe oligospermic males.,disease:AZFc deletions in the Yq11.23 region, including the DAZ genes, are a cause of azoospermia or oligospermia. They lead to male infertility due to impaired spermatogenesis and are found 2-10% of azoospermic or severe oligospermic males. Some AZFc deletions remove only the DAZ and DAZ2 genes and cause severe oligozoospermia.,domain:The DAZ-like repeats are essential and mediate the interaction with DAZAP1 and DAZAP2.,function:RNA-binding protein that plays an e

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