硕肯生物硕肯生物Soken.bio
查看试用产品 →开放浏览 · 登录后申请
抗人 MRP2 抗体对
试剂盒

抗人 MRP2 抗体对

01AB02375

ATP binding cassette subfamily C member 2 (MRP2) is an ATP-dependent efflux transporter that mediates the export of a wide range of organic anions, including conjugated bilirubin, bile salts, and various drug conjugates. It is predominantly localized to the apical membrane of hepatocytes, as well as the renal proximal tubule and intestinal epithelial cells, where it facilitates hepatic detoxification and biliary excretion. Structurally, MRP2 consists of two transmembrane domains, two nucleotide-binding domains, and a regulatory domain that modulates substrate selectivity and transport activity. This transporter plays a critical role in chemoprotection and drug disposition. Pathogenic variants in the ABCC2 gene cause Dubin-Johnson syndrome, a condition characterized by conjugated hyperbilirubinemia. Additionally, alterations in MRP2 expression or function are associated with multidrug resistance in various cancers.

Human
规格起售价
登录后可查看

技术参数

靶点基因名
ABCC2
基因别名
CMOAT; CMOAT1; CMRP; MRP2
蛋白别名
ATP binding cassette subfamily C member 2; MRP2
UniProt
Q92887
物种
Human

产品详情

靶点名称
MRP2
蛋白名称
ATP binding cassette subfamily C member 2
蛋白别名
ATP-binding cassette sub-family C member 2; Canalicular multidrug resistance protein; Canalicular multispecific organic anion transporter 1; Multidrug resistance-associated protein 2
靶点基因名
ABCC2
基因别名
CMOAT; CMOAT1; CMRP; MRP2
UniProt
Q92887
来源物种
Homo sapiens (Human)
物种反应性
Human

背景介绍

ATP binding cassette subfamily C member 2 (MRP2) is an ATP-dependent efflux transporter that mediates the export of a wide range of organic anions, including conjugated bilirubin, bile salts, and various drug conjugates. It is predominantly localized to the apical membrane of hepatocytes, as well as the renal proximal tubule and intestinal epithelial cells, where it facilitates hepatic detoxification and biliary excretion. Structurally, MRP2 consists of two transmembrane domains, two nucleotide-binding domains, and a regulatory domain that modulates substrate selectivity and transport activity. This transporter plays a critical role in chemoprotection and drug disposition. Pathogenic variants in the ABCC2 gene cause Dubin-Johnson syndrome, a condition characterized by conjugated hyperbilirubinemia. Additionally, alterations in MRP2 expression or function are associated with multidrug resistance in various cancers.