PDGFR beta Rabbit Monoclonal Antibody(C1723)
WB | 1:500 - 1:1000 |
IHC | 1:500 - 1:200 |
IF/ICC | 1:50 - 1:200 |
IP | 1:10 - 1:50 |
Description | Recombinant rabbit monoclonal antibody to PDGFR beta |
Specificity | Recognizes endogenous levels of PDGFR beta protein |
Antibody Type | Primary antibody, Recombinant |
Imnunogen | KLH-conjugated synthetic peptide encompassing a sequence within human PDGFR beta protein. The exact sequence is proprietary. |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 123 kD; Observed: 170 kD |
Form/Buffer | Liquid in PBS, pH 7.4, containing 50% glycerol, 0.2% BSA and 0.01% sodium azide. |
Alternative Names | PDGFR; PDGFR1; Platelet-derived growth factor receptor beta; PDGF-R-beta; PDGFR-beta; Beta platelet-derived growth factor receptor; Beta-type platelet-derived growth factor receptor; CD140 antigen-like family member B; Platelet-derived growth factor receptor 1; PDGFR-1; CD140b |
Gene Symbol | PDGFRB |
Entrez Gene | 5159(Human); 18596(Mouse); 24629(Rat) |
SwissProt | P09619(Human); P05622(Mouse); Q05030(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of PDGFR beta expression in U87 (A), HepG2 (B), Hela (C), mouse kidney (D), mouse kidney (E), rat brain (F), rat liver whole cell lysates. (Predicted band size: 123 kD; Observed band size: 170 kD)

Immunohistochemical analysis of PDGFR beta staining in human uterus formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of PDGFR beta staining in Hela cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a AREX® Fluor 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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