JAK2 (Phospho-Y1007) Rabbit Polyclonal Antibody
WB | 1:500 - 1:1000 |
IHC | 1:50 - 1:200 |
IF/ICC | 1:50 - 1:200 |
Description | Rabbit polyclonal antibody to JAK2 (Phospho-Y1007) |
Specificity | Recognizes endogenous levels of JAK2 protein only when phosphorylated at Y1007. |
Antibody Type | Primary antibody |
Imnunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding Y1007 of human JAK2 protein. The exact sequence is proprietary. |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 130 kD; Observed: 130 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 | Tyrosine-protein kinase JAK2; Janus kinase 2; JAK-2 |
Gene Symbol | JAK2 |
Entrez Gene | 3717(Human); 16452(Mouse); 24514(Rat) |
SwissProt | O60674(Human); Q62120(Mouse); Q62689(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of JAK2 (Phospho-Y1007) expression in HeLa (A), TF1 (B), NIH3T3 (C), rat kidney (D) whole cell lysates. (Predicted band size: 130 kD; Observed band size: 130 kD)

Immunohistochemical analysis of JAK2 (Phospho-Y1007) 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 JAK2 (Phospho-Y1007) staining in Jurkat 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 AREX® Fluor 488 -conjugated secondary antibody (green) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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