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Anti-GLUR4 (Phospho-S862) Antibody

Catalog Number: orb214009

DispatchUsually dispatched within 5-10 working days
$ 160.00
Catalog Numberorb214009
CategoryAntibodies
DescriptionRabbit polyclonal antibody to GRIA4
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, WB
ReactivityHuman, Mouse, Primate, Rat, Zebrafish
ImmunogenKLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S862 of human GLUR4 protein. The exact sequence is proprietary.
Antibody TypePrimary Antibody
Dilution rangeWB: 1-500-1-1000
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetGRIA4
Entrez14802, 29629, 2893
UniProt IDP48058, Q9Z2W8, P19493
SourceRabbit
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti GLUR4 antibody, anti Glutamate receptor 4 ant
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-GLUR4 (Phospho-S862) Antibody

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)

Anti-GLUR4 (Phospho-S862) Antibody

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 (Phospho-H 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.

Anti-GLUR4 (Phospho-S862) Antibody

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).