WB, IP
H
Endogenous
130-180
Rabbit IgG
#P08183
5243
Product Information
Product Usage Information
Application | Dilution |
---|---|
Western Blotting | 1:1000 |
Immunoprecipitation | 1:50 |
Storage
Specificity / Sensitivity
Species Reactivity:
Human
Species predicted to react based on 100% sequence homology
The antigen sequence used to produce this antibody shares
100% sequence homology with the species listed here, but
reactivity has not been tested or confirmed to work by CST.
Use of this product with these species is not covered under
our
Product Performance Guarantee.
Monkey
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human MDR1 protein.
Background
MDR1/ABCB1 belongs to the Mdr/Tap subfamily of the ATP-binding cassette transporter superfamily (1). Multidrug resistance 1 (MDR1) serves as an efflux pump for xenobiotic compounds with broad substrate specificity. MDR1 substrates include therapeutic agents such as actinomycin D, etoposide, imatinib, and doxorubicin, as well as endogenous molecules including β-amyloids, steroid hormones, lipids, phospholipids, cholesterol, and cytokines (2). Research studies have shown that MDR1 reduces drug accumulation in cancer cells, allowing the development of drug resistance (3-5). On the other hand, MDR1 expressed in the plasma membrane of cells in the blood-brain, blood-cerebral spinal fluid, or blood-placenta barriers restricts the permeability of drugs into these organs from the apical or serosal side (6,7). MDR1 is also expressed in normal tissues with excretory function such as small intestine, liver, and kidney (7). Intracellular MDR1 has been detected in the ER, vesicles, and nuclear envelope, and has been associated with cell trafficking machinery (8). Other reported functions of MDR1 include viral resistance, cytokine trafficking (9,10), and lipid homeostasis in the peripheral and central nervous system (11-13).
- Furuya, K.N. et al. (1997) Cancer Res 57, 3708-16.
- Litman, T. et al. (1997) Biochim Biophys Acta 1361, 169-76.
- Chen, C.J. et al. (1986) Cell 47, 381-9.
- Kartner, N. et al. (1983) Cancer Res 43, 4413-9.
- Chen, G. et al. (1997) J Biol Chem 272, 5974-82.
- Brinkmann, U. and Eichelbaum, M. (2001) Pharmacogenomics J 1, 59-64.
- Fromm, M.F. (2004) Trends Pharmacol Sci 25, 423-9.
- Miller, D.S. et al. (2008) Pharmacol Rev 60, 196-209.
- Ambudkar, S.V. et al. (1999) Annu Rev Pharmacol Toxicol 39, 361-98.
- Raviv, Y. et al. (2000) FASEB J 14, 511-5.
- Meijer, O.C. et al. (2003) J Endocrinol 178, 13-8.
- Karssen, A.M. et al. (2002) J Endocrinol 175, 251-60.
- Jeannesson, E. et al. (2009) Clin Chim Acta 403, 198-202.
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
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
Limited Uses
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