Description: Rabbit polyclonal antibody to Beta-2 Adrenergic Receptor (Phospho-S346) Immunogen: KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S346 of human Beta-2 Adrenergic Receptor protein. The exact sequence is proprietary. Purification: The antibody was purified by immunogen affinity chromatography. Clonality: Polyclonal Form: 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), IH (1/50 - 1/100), IF/IC (1/50 - 1/200) Gene Symbol: ADRB2 Alternative Names: ADRB2R; B2AR; Beta-2 adrenergic receptor; Beta-2 adrenoreceptor; Beta-2 adrenoceptorEntrez Gene (Human): 154Entrez Gene (Mouse) : 11555SwissProt (Human): P07550SwissProt (Mouse) : P18762SwissProt (Rat) : P10608Storage/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 Beta-2 Adrenergic Receptor (Phospho-S346) expression in PC3 (A), HepG2 (B), HEK293T (C) whole cell lysates.
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Immunohistochemical analysis of Beta-2 Adrenergic Receptor (Phospho-S346) staining in human brain 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.
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Immunofluorescent analysis of Beta-2 Adrenergic Receptor (Phospho-S346) 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 hidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark.
Intermittent maternofetal oxygenation during late gestation improved birthweight, neonatal growth, body symmetry, and muscle metabolism in intrauterine growth-restricted lambs