Revision 1

#4446Store at -20C

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
Applications:

WB, IP, IF-IC

REACTIVITY:

H

SENSITIVITY:

Endogenous

MW (kDa):

> 200

SOURCE:

Rabbit

UniProt ID:

#Q92887

Entrez-Gene Id:

1244

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:100
Immunofluorescence (Immunocytochemistry) 1:800

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA and 50% glycerol. Store at –20°C. Do not aliquot the antibody.

Specificity / Sensitivity

MRP2/ABCC2 (R260) Antibody detects endogenous levels of total MRP2 protein.

Species Reactivity:

Human

Source / Purification

Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Arg260 of human MRP2 protein. Antibodies were purified by protein A and peptide affinity chromatography.

Background

Multi-drug resistance protein 2 (MRP2), also known as cMRP, cMOAT, and ABCC2, is an ATP binding cassette (ABC) transporter and part of the multi-drug resistance (MRP) family (1,2). The MRP proteins are membrane proteins that function as organic anion pumps involved in the cellular removal of cancer drugs (2). MRP2 is associated with resistance to a number of cancer drugs, such as cisplatin, etoposide, doxorubicin, and methotrexate (3-5). MRP2 is predominately expressed on the apical membranes in the liver (6-9) and kidney proximal tubules (10). It is responsible for the ATP-dependent secretion of bilirubin glucuronides and other organic anions from hepatocytes into the bile, a process important for the excretion of endogenous and xenobiotic substances. Loss of MRP2 activity is the cause of Dubin-Johnson syndrome, an autosomal recessive disorder characterized by defects in the secretion of anionic conjugates and the presence of melanin like pigments in hepatocytes (11-13).

  1. Keppler, D. and Konig, J. (1997) FASEB J 11, 509-16.
  2. Borst, P. et al. (2000) J Natl Cancer Inst 92, 1295-302.
  3. Taniguchi, K. et al. (1996) Cancer Res 56, 4124-9.
  4. Hooijberg, J.H. et al. (1999) Cancer Res 59, 2532-5.
  5. Cui, Y. et al. (1999) Mol Pharmacol 55, 929-37.
  6. Büchler, M. et al. (1996) J Biol Chem 271, 15091-8.
  7. Paulusma, C.C. et al. (1996) Science 271, 1126-8.
  8. Mayer, R. et al. (1995) J Cell Biol 131, 137-50.
  9. Ito, K. et al. (1998) J Biol Chem 273, 1684-8.
  10. Schaub, T.P. et al. (1997) J Am Soc Nephrol 8, 1213-21.
  11. Dubin, I.N. and Johnson, F.B. (1954) Medicine (Baltimore) 33, 155-97.
  12. Kartenbeck, J. et al. (1996) Hepatology 23, 1061-6.
  13. Paulusma, C.C. et al. (1997) Hepatology 25, 1539-42.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Western Blot Buffer

IMPORTANT: For western blots, incubate membrane with diluted primary antibody in 5% w/v BSA, 1X TBS, 0.1% Tween® 20 at 4°C with gentle shaking, overnight.

Applications Key

WB: Western Blotting IP: Immunoprecipitation IF-IC: Immunofluorescence (Immunocytochemistry)

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

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