Description:Rabbit polyclonal antibody to GHRH ReceptorImmunogen:KLH-conjugated synthetic peptide encompassing a sequence within the C-term region of human GHRH Receptor. The exact sequence is proprietary.Purification:The antibody was purified by immunogen affinity chromatography.Clonality:PolyclonalForm:Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.Dilution:WB (1/500 - 1/1000), IF/IC (1/100 - 1/500)Gene Symbol:GHRHRAlternative Names:Growth hormone-releasing hormone receptor; GHRH receptor; Growth hormone-releasing factor receptor; GRF receptor; GRFR
Entrez Gene (Human):
    2692;
Entrez Gene (Mouse):
    14602;
Entrez Gene (Rat):
    25321;
SwissProt (Human):
Q02643;
SwissProt (Mouse):
    P32082;
SwissProt (Rat):
    Q02644;
Storage/Stability:Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
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             Western blot analysis of GHRH Receptor expression in mouse kidney (A), rat kidney (B) whole cell lysates. (Predicted band size: 47 kD; Observed band size: 47; 55 kD) Western blot analysis of GHRH Receptor expression in mouse kidney (A), rat kidney (B) whole cell lysates. (Predicted band size: 47 kD; Observed band size: 47; 55 kD)
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             Immunofluorescent analysis of GHRH Receptor staining in LOVO 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue). Immunofluorescent analysis of GHRH Receptor staining in LOVO 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 DyLight 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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