ZAP70 (Phospho-Y315) Rabbit Polyclonal Antibody
WB | 1:500 - 1:1000 |
IHC | 1:50 - 1:100 |
IF/ICC | 1:50 - 1:200 |
Description | Rabbit polyclonal antibody to ZAP70 (Phospho-Y315) |
Specificity | Recognizes endogenous levels of ZAP70 protein only when phosphorylated at Y315. |
Antibody Type | Primary antibody |
Imnunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding Y315 of human ZAP70 protein. The exact sequence is proprietary. |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 69 kD; Observed: 70 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 | SRK; Tyrosine-protein kinase ZAP-70; 70 kDa zeta-chain associated protein; Syk-related tyrosine kinase |
Gene Symbol | ZAP70 |
Entrez Gene | 7535(Human); 22637(Mouse) |
SwissProt | P43403(Human); P43404(Mouse) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of ZAP70 (Phospho-Y315) expression in Jurkat H2O2-treated (A), HeLa H2O2-treated (B), Ramos lambda phosphatase-treated (C), mouse kidney (D), rat kidney (E) whole cell lysates. (Predicted band size: 69 kD; Observed band size: 70 kD)

Immunohistochemical analysis of ZAP70 (Phospho-Y315) staining in human lymph node 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 ZAP70 (Phospho-Y315) 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 AREX® Fluor 488 -conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AREX® Fluor 594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
FAQs
New Products
Datasheet
