6080yyy午夜理论av片,黄片aaawww,国产色婷婷激情片,久久午夜国产精品,久久色av网址导航,销魂美女做爰免费视频,日韩黄色三级电影在线观看,在线电影人妻在线观看,日本高清成人片www网站免费,长途公共汽车上的轮杆

歡迎來到上海通蔚!

021-54845833/15800441009

品質(zhì)保證 · 通蔚試劑

當(dāng)前位置: 首頁 > 科研產(chǎn)品 > 科研抗體 > 其他抗體 > SPATA19 抗原(重組蛋白)

產(chǎn)品中心

  • SPATA19 抗原(重組蛋白)

    規(guī)格:
    數(shù)量:

    購買數(shù)量

    價格:
    • 品牌 : 通蔚生物
    • 目錄號 : TW17674
    • 應(yīng)用 : 僅供科研使用
    • 保存條件 : 低溫保存
    • 貨期 : 現(xiàn)貨
    • 商品庫存:90
  • 商品詳情
  • 參考文獻(xiàn)
  • 說明書下載
  • 商品評論0
  • 相關(guān)產(chǎn)品

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℃)

相關(guān)類別 抗原

概  述:

Fusion protein corresponding to a region derived from 27-167 amino acids of human SPATA19


技術(shù)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.