MRP2 rabbit pAb

MRP2 rabbit pAb

AO-06-ES4715-50

MRP2 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES4715
Product nameMRP2 rabbit pAb
ReactivityHuman;Rat;Mouse;
ApplicationsWB;ELISA
Other nameABCC2; CMOAT; CMOAT1; CMRP; MRP2; Canalicular multispecific organic anion transporter 1; ATP-binding cassette sub-family C member 2; Canalicular multidrug resistance protein; Multidrug resistance-associated protein 2
Size50μL
Unit price ($)148
Human gene ID1244
Human Swiss-ProtQ92887
SourceRabbit
IsotypeIgG
TargetMRP2
Fields>>Antifolate resistance;>>Platinum drug resistance;>>ABC transporters;>>Bile secretion
Gene nameABCC2
Protein nameCanalicular multispecific organic anion transporter 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID
Mouse gene link
Mouse Swiss-ProtQ8VI47
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human ABCC2. AA range:991-1040
SpecificityMRP2 Polyclonal Antibody detects endogenous levels of MRP2 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)175kD
BackgroundThe 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, Jul 2008],
Functiondisease: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.,function:Mediates hepatobiliary excretion of numerous organic anions. May function as a cellular cisplatin transporter.,similarity:Belongs to the ABC transporter family. Conjugate transporter (TC 3.A.1.208) subfamily.,similarity:Contains 2 ABC transmembrane type-1 domains.,similarity:Contains 2 ABC transporter domains.,tissue specificity:Found on the apical membrane of polarized cells in liver, kidney and intestine. The highest expression is found in liver.,
Subcellular locationApical cell membrane ; Multi-pass membrane protein .
ExpressionExpressed by polarized cells in liver, kidney and intestine. The highest expression is found in liver.

Additional Images

Image 1
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Western Blot analysis of 3T3 cells using MRP2 Polyclonal Antibody diluted at 1:1000
Image 2
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Western blot analysis of ABCC2 Antibody. The lane on the right is blocked with the ABCC2 peptide.
Image 3
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Western blot analysis of the lysates from HeLa cells using ABCC2 antibody.
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: AO-06-ES4715-50
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Hurry! only 10 items left in stock.

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