CREB (Phospho-S129) kanin polyklonal antikropp
WB | 1:500 - 1:2000 |
IHC | 1:50 - 1:200 |
IF/ICC | 1:50 - 1:100 |
Beskrivning | Kanin polyklonal antikropp mot CREB (Phospho-S129) |
Specificitet | Känner igen endogena nivåer av CREB-protein endast när det fosforyleras vid S129. |
Antikroppstyp | Primär antikropp |
Imnunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding S129 of human CREB protein. The exact sequence is proprietary. |
Rening | Antikroppen renades genom immunogenaffinitetskromatografi. |
Molekylvikt | Förutspått: 35 kD; Observerad: 38 kD |
Form/buffert | Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Alternativa namn | Cyclic AMP-responsive element-binding protein 1; CREB-1; cAMP-responsive element-binding protein 1 |
Gensymbol | CREB1 |
Entrez Gene | 1385 (Human); 12912(mus); 81646(råtta) |
SwissProt | P16220 (Human); Q01147(mus); P15337(råtta) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of CREB (Phospho-S129) expression in RAW264.7 UV-treated (A) whole cell lysates. (Predicted band size: 35 kD; Observed band size: 38 kD)

Immunohistochemical analysis of CREB (Phospho-S129) 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 CREB (Phospho-S129) staining in RAW264.7 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.
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