GSK3 alpha (Phospho-S21) Rabbit Polyclonal Antibody
WB | 1:500 - 1:1000 |
IHC | 1:100 - 1:200 |
IF/ICC | 1:100 - 1:500 |
IP | 1:10 - 1:100 |
Description | Rabbit polyclonal antibody to GSK3 alpha (Phospho-S21) |
Specificity | Recognizes endogenous levels of GSK3 alpha protein only when phosphorylated at S21. |
Antibody Type | Primary antibody |
Imnunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S21 of human GSK3 alpha protein. The exact sequence is proprietary. |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 50 kD; Observed: 51 kD |
Form/Buffer | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Alternative Names | Glycogen synthase kinase-3 alpha; GSK-3 alpha; Serine/threonine-protein kinase GSK3A |
Gene Symbol | GSK3A |
Entrez Gene | 2931(Human); 606496(Mouse); 50686(Rat) |
SwissProt | P49840(Human); Q2NL51(Mouse); P18265(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of GSK3 alpha (Phospho-S21) expression in Hela (A), H466 (B) whole cell lysates. (Predicted band size: 50 kD; Observed band size: 51 kD)

Immunohistochemical analysis of GSK3 alpha (Phospho-S21) 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 GSK3 alpha (Phospho-S21) staining in PC12 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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