ABCC2 polyclonal antibody (A01)-抗体-抗体-生物在线
亚诺法生技股份有限公司(Abnova)
ABCC2 polyclonal antibody (A01)

ABCC2 polyclonal antibody (A01)

商家询价

产品名称: ABCC2 polyclonal antibody (A01)

英文名称: ABCC2 polyclonal antibody (A01)

产品编号: H00001244-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
  • 电话 : +886-920**1152 点击查看
  • 传真 : 点击查看
  • 邮箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a partial recombinant ABCC2.
  • Immunogen:
  • ABCC2 (NP_000383, 214 a.a. ~ 313 a.a) partial recombinant protein with GST tag.
  • Sequence:
  • LKGYKRPLTLEDVWEVDEEMKTKTLVSKFETHMKRELQKARRALQRRQEKSSQQNSGARLPGLNKNQSQSQDALVLEDVEKKKKKSGTKKDVPKSWLMKA
  • 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.
  • Applications
  • ELISA
  • Application Image
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 1244
  • Gene Name:
  • ABCC2
  • Gene Alias:
  • ABC30,CMOAT,DJS,KIAA1010,MRP2,cMRP
  • Gene Description:
  • ATP-binding cassette, sub-family C (CFTR/MRP), member 2
  • 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 is expressed in the canalicular (apical) part of the hepatocyte and functions in biliary transport. Substrates include anticancer drugs such as vinblastine; therefore, this protein appears to contribute to drug resistance in mammalian cells. Several different mutations in this gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000020267,canalicular multispecific organic anion transporter
  • Gene Pathway

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