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MRP2 Antibody Blocking Peptide

(bs-1092P)-500ug
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  • bs-1092P
  • 2025年10月16日
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      500ug

    产品编号bs-1092P
    英文名称MRP2 Antibody Blocking Peptide
    中文名称多药耐药相关蛋白2封闭多肽
    英文别名multidrug resistance-associated protein2; ABC30; ABCC2; ATP binding cassette sub family C (CFTR/MRP) member 2; ATP binding cassette subfamily C member 2; Canalicular multidrug resistance protein; Canalicular multispecific organic anion transporter 1; CMOAT; CMOAT1; cMRP; DJS; KIAA1010; MRP 2; MRP-2; MRP2; Multidrug resistance associated protein 2; MRP2_HUMAN; ATP-binding cassette sub-family C member 2; Multidrug resistance-associated protein 2.
    性状Lyophilized
    纯化方法HPLC
    研究领域

    Cancer > Drug resistance > MRP-related proteins

    Signal Transduction > Metabolism > Plasma Membrane > Channels

    亚细胞定位Membrane; Multi-pass membrane protein.
    组织特异性Found on the apical membrane of polarized cells in liver, kidney and intestine. The highest expression is found in liver.
    相似性Belongs to the ABC transporter superfamily. ABCC family. Conjugate transporter (TC 3.A.1.208) subfamily.
    Contains 2 ABC transmembrane type-1 domains.
    Contains 2 ABC transporter domains.
    功能Mediates hepatobiliary excretion of numerous organic anions. May function as a cellular cisplatin transporter.
    保存条件Shipped at 4℃. Stored at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    背景资料multidrug resistance-associated protein 2 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. Belongs to the ABC transporter family.

     

     

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