Immunohistochemical analysis of CK1 alpha (Phospho-Y321) staining in human colon 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.
Western blotting analysis of CK1 alpha (Phospho-Y321) expression in HEK293T UV-treated (A), Jurkat (B), K562 (C), mouse liver (D), H9C2 UV-treated (E) whole cell lysates.
Species Reactivity: Human, mouse, rat, chicken, pig, zebrafish
Applications Tested: Western blotting (WB), immunohistochemistry (IHC)
Immunogen
A synthesized peptide derived from human Phospho-CK1 alpha (Y321)
Isotype
Rabbit IgG
Storage Buffer
Supplied in PBS (pH 7.3) containing 30% glycerol, and 0.01% sodium azide.
Storage
Store at -20 °C for one year.
Recommended Dilutions
Western Blotting (WB): 1:500-1:1,000 Immunohistochemistry (IHC): 1:50-1:100
Note
This product is for research use only.
Picture
Immunohistochemical analysis of CK1 alpha (Phospho-Y321) staining in human colon 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.
Western blotting analysis of CK1 alpha (Phospho-Y321) expression in HEK293T UV-treated (A), Jurkat (B), K562 (C), mouse liver (D), H9C2 UV-treated (E) whole cell lysates.
Immunohistochemical analysis of CK1 alpha (Phospho-Y321) staining in human colon 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.
Western blotting analysis of CK1 alpha (Phospho-Y321) expression in HEK293T UV-treated (A), Jurkat (B), K562 (C), mouse liver (D), H9C2 UV-treated (E) whole cell lysates.
