MKI67IP (Phospho-T234) Rabbit Polyclonal Antibody
WB | 1:500 - 1:2000 |
IHC | 1:50 - 1:200 |
IF/ICC | 1:50 - 1:100 |
Description | Rabbit polyclonal antibody to MKI67IP (Phospho-T234) |
Specificity | Recognizes endogenous levels of MKI67IP protein only when phosphorylated at T234. |
Antibody Type | Primary antibody |
Imnunogen | KLH-conjugated synthetic phosphopeptide corresponding to residues surrounding T234 of human MKI67IP protein. The exact sequence is proprietary. |
Purification | The antibody was purified by immunogen affinity chromatography. |
Molecular Weight | Predicted: 34 kD; Observed: 36 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 | MKI67IP; NOPP34; MKI67 FHA domain-interacting nucleolar phosphoprotein; Nucleolar phosphoprotein Nopp34; Nucleolar protein interacting with the FHA domain of pKI-67; hNIFK |
Gene Symbol | MKI67IP |
Entrez Gene | 84365(Human); 67949(Mouse); 246042(Rat) |
SwissProt | Q9BYG3(Human); Q91VE6(Mouse); Q5RJM0(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of MKI67IP (Phospho-T234) expression in HGC27 (A), H446 (B) whole cell lysates. (Predicted band size: 34 kD; Observed band size: 36 kD)

Immunohistochemical analysis of MKI67IP (Phospho-T234) staining in human brain 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 MKI67IP (Phospho-T234) 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 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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