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Rabbit Anti-MRP2  antibody (bsm-61068R)
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说明书: 50ul  100ul  
50ul/1580.00元
100ul/2500.00元
大包装/询价

产品编号 bsm-61068R
英文名称 Rabbit Anti-MRP2  antibody
中文名称 多药耐药相关蛋白2抗体
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.  
抗体来源 Rabbit
克隆类型 Monoclonal
交叉反应 Human
产品应用 WB=1:500-2000,IHC-P=1:200-500,IHC-F=1:100-400,Flow-Cyt=1:100,ICC=1:50-200,IF=1:100-400
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 174kDa
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MRP2 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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.

Function:
Mediates hepatobiliary excretion of numerous organic anions. May function as a cellular cisplatin transporter.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Found on the apical membrane of polarized cells in liver, kidney and intestine. The highest expression is found in liver.

DISEASE:
Defects in ABCC2 are the cause of Dubin-Johnson syndrome (DJS) [MIM:237500]. DJS is an autosomal recessive disorder characterized by conjugated hyperbilirubinemia, an increase in the urinary excretion of coproporphyrin isomer I, deposition of melanin-like pigment in hepatocytes, and prolonged retention of sulfobromophthalein, but otherwise normal liver function.

Similarity:
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.

SWISS:
Q8VI47

Gene ID:
12780

Database links:

Entrez Gene: 1244 Human

Entrez Gene: 12780 Mouse

Entrez Gene: 25303 Rat

Omim: 601107 Human

SwissProt: Q92887 Human

SwissProt: Q8VI47 Mouse

SwissProt: Q63120 Rat

Unigene: 368243 Human

Unigene: 39054 Mouse

Unigene: 10265 Rat



MRP-2作为一种结合输出泵,转运许多不同的药物结合物的蛋白。
MRP2蛋白的染色阳性产物分布于细胞浆/膜中。
产品图片
Paraformaldehyde-fixed, paraffin embedded Human Liver; Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15 min; Antibody incubation with MRP2 Monoclonal Antibody, Unconjugated(bsm-61068R) at 1:200 overnight at 4°C, followed by conjugation to the SP Kit (Rabbit, SP-0023) and DAB (C-0010) staining DAB staining.
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