Description：Rabbit polyclonal antibody to GLUR4 (Phospho-S862)Immunogen：KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S862 of human GLUR4 protein. 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), IH (1/50 - 1/100), IF/IC (1/50 - 1/200)Gene Symbol：GRIA4Alternative Names：GLUR4; Glutamate receptor 4; GluR-4; GluR4; AMPA-selective glutamate receptor 4; GluR-D; Glutamate receptor ionotropic, AMPA 4; GluA4 Entrez Gene (Human)： 2893; Entrez Gene (Mouse)： 14802; Entrez Gene (Rat)： 29629; SwissProt (Human)： P48058; SwissProt (Mouse)： Q9Z2W8; SwissProt (Rat)： P19493; 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 GLUR4 (Phospho-S862) expression in HEK293T (A), rat brain (B), mouse brain (C), MCF7 (D) whole cell lysates. (Predicted band size: 100 kD; Observed band size: 100 kD)
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  Immunohistochemical analysis of GLUR4 (Phospho-S862) 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 GLUR4 (Phospho-S862) staining in MCF7 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 AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).