ABCC8 polyclonal antibody (A01)-抗体-抗体-生物在线
亚诺法生技股份有限公司（Abnova)
ABCC8 polyclonal antibody (A01)

ABCC8 polyclonal antibody (A01)

商家询价

产品名称： ABCC8 polyclonal antibody (A01)

英文名称： ABCC8 polyclonal antibody (A01)

产品编号： H00006833-A01

产品价格： null

产品产地： 台湾

品牌商标： Abnova

更新时间： null

使用范围：

亚诺法生技股份有限公司（Abnova)
  • 联系人 :
  • 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
  • 邮编 : 11493
  • 所在区域 : 台湾
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  • 邮箱 : sales@abnova.com.tw
进入展台

  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a partial recombinant ABCC8.
  • Immunogen:
  • ABCC8 (NP_000343, 611 a.a. ~ 710 a.a) partial recombinant protein with GST tag.
  • Sequence:
  • SEFLSSAEIREEQCAPHEPTPQGPASKYQAVPLRVVNRKRPAREDCRGLTGPLQSLVPSADGDADNCCVQIMGGYFTWTPDGIPTLSNITIRIPRGQLTM
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Storage Buffer:
  • 50 % glycerol
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00006833-A01
    Western Blot detection against Immunogen (37.11 KDa) .
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Recombinant protein)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 6833
  • Gene Name:
  • ABCC8
  • Gene Alias:
  • ABC36,HHF1,HI,HRINS,MRP8,PHHI,SUR,SUR1,TNDM2
  • Gene Description:
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 8
  • Gene Summary:
  • The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions as a modulator of ATP-sensitive potassium channels and insulin release. Mutations and deficiencies in this protein have been observed in patients with hyperinsulinemic hypoglycemia of infancy, an autosomal recessive disorder of unregulated and high insulin secretion. Mutations have also been associated with non-insulin-dependent diabetes mellitus type II, an autosomal dominant disease of defective insulin secretion. Alternative splicing of this gene has been observed; however, the transcript variants have not been fully described. [provided by RefSeq
  • Other Designations:
  • ATP-binding cassette, sub-family C, member 8,sulfonylurea receptor (hyperinsulinemia)

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