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Item 1 of 3
Anti-SGK1 (Phospho-S422) Antibody
Catalog Number: orb393192
| Catalog Number | orb393192 |
|---|---|
| Category | Antibodies |
| Description | Rabbit polyclonal antibody to SGK1 (Phospho-S422) |
| Target | SGK1 |
| Clonality | Polyclonal |
| Species/Host | Rabbit |
| Conjugation | Unconjugated |
| Reactivity | Human, Mouse, Primate |
| Form/Appearance | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
| Buffer/Preservatives | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
| Immunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S422 of human SGK1 protein. The exact sequence is proprietary. |
| UniProt ID | O00141 |
| Tested applications | IF, IH, WB |
| Dilution range | WB: 1:500:1000, IHC-P: 1:100:200, IF/ICC: 1:100:500 |
| Antibody Type | Primary Antibody |
| Source | Rabbit |
| Storage | Maintain 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. |
| Alternative names | SGK; Serine/threonine-protein kinase Sgk1; Serum/g Read more... |
| Note | For research use only |
| Entrez | 6446 |
Western blot analysis of SGK1 (Phospho-S422) expression in AML12 (A), LO2 (B), MCF7 (C) whole cell lysates. (Predicted band size: 48 kD; Observed band size: 54 kD)
Immunohistochemical analysis of SGK1 (Phospho-S422) staining in human prostate cancer 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.
Immunofluorescent analysis of SGK1 (Phospho-S422) 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).
