WB result of MDR1/ABCB1 Rabbit mAb
Primary antibody: MDR1/ABCB1 Rabbit mAb at 1/1000 dilution
Lane 1: unboiled SH-SY5Y whole cell lysate 10 µg
Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 141 kDa
Observed MW: 180 kDa
Product Details
Product Details
Product Specification
Host | Rabbit |
Synonyms | ATP-dependent translocase ABCB1, TP-binding cassette sub-family B member 1, Multidrug resistance protein 1, P-glycoprotein 1, Phospholipid transporter ABCB1, CD243, PGY1 |
Immunogen | Recombinant Protein |
Location | Cytoplasm, Cell membrane |
Accession | P08183 |
Clone Number | SDT-872-21 |
Antibody Type | Recombinant mAb |
Isotype | IgG |
Application | WB, IHC-P |
Reactivity | Hu |
Purification | Protein A |
Concentration | 0.5 mg/ml |
Conjugation | Unconjugated |
Physical Appearance | Liquid |
Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
application | dilution | species |
WB | 1:1000 | |
IHC-P | 1:500-1:1000 |
Background
MDR1 is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. MDR1 is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is an ATP-dependent drug efflux pump for xenobiotic compounds with broad substrate specificity. It is responsible for decreased drug accumulation in multidrug-resistant cells and often mediates the development of resistance to anticancer drugs. This protein also functions as a transporter in the blood-brain barrier.
Picture
Picture
Western Blot
Immunohistochemistry


IHC shows positive staining in paraffin-embedded human kidney. Anti-MDR1/ABCB1 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.





