Anti-PLA2G4A (Phospho-S505) Antibody 
Datasheet
MSDS
Description: Rabbit polyclonal antibody to PLA2G4A (Phospho-S505) Immunogen: KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S505 of human PLA2G4A 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 (1/100 - 1/200), IF/IC (1/100 - 1/500) Gene Symbol: PLA2G4A Alternative Names: CPLA2; PLA2G4; Cytosolic phospholipase A2; cPLA2; Phospholipase A2 group IVAEntrez Gene (Human): 5321Entrez Gene (Mouse) : 18783SwissProt (Human): P47712SwissProt (Mouse) : P47713SwissProt (Rat) : P50393Storage/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 PLA2G4A (Phospho-S505) expression in Hela (A), mouse brain (B), rat kidney (C) whole cell lysates. -
Immunohistochemical analysis of PLA2G4A (Phospho-S505) staining in human breast cancer 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 PLA2G4A (Phospho-S505) 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 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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