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  • 產(chǎn)品名稱：SPATA19 抗原（重組蛋白）

  • 產(chǎn)品型號：100ug
  • 產(chǎn)品廠商：通蔚生物
  • 產(chǎn)品價格：800
  • 產(chǎn)品庫存：35
  • 產(chǎn)品文檔：
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詳情介紹：

中文名稱： SPATA19 抗原（重組蛋白）

英文名稱： SPATA19 Antigen (Recombinant Protein)

別     名：  spermatogenesis associated 19; CT132; SPAS1; spergen1

儲     存：  冷凍（-20℃）

儲     存：  冷凍（-20℃）

相關類別： 抗原

概     述：
 
Fusion protein corresponding to a region derived from 27-167 amino acids of human SPATA19
   
技術規(guī)格

Full name:

spermatogenesis associated 19

Synonyms:

CT132; SPAS1; spergen1

Swissprot:

Q7Z5L4

Gene Accession:

BC058039

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

SPATA19(spermatogenesis associated 19), also known as spergen1 (spermatogenic cell-specific gene 1 protein), CT132 or SPAS1, is a 167 amino acid mitochondrial outer membrane protein suggested to function in spermiogenesis. Expressed specifically in testis, SPATA19 is encoded by a gene that maps to human chromosome 11, which comprises approximately 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxiatelangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms’ tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.





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