A. Western blot analysis on HeLa cell lysates using anti-Phospho-Pin1 (pS16) RabMAb (Cat. #AJ1611b), 1:500 dilution. Cells were either (A) untreated or (B) treated with FBS + Calyculin A.
Essential PPIase that regulates mitosis presumably by interacting with NIMA and attenuating its mitosis-promoting activity. Displays a preference for an acidic residue N-terminal to the isomerized proline bond. Catalyzes pSer/Thr-Pro cis/trans isomerizations. Down-regulates kinase activity of BTK. Can transactivate multiple oncogenes and induce centrosome amplification, chromosome instability and cell transformation Required for the efficient dephosphorylation and recycling of RAF1 after mitogen activation
Tissue Specificity
The phosphorylated form at Ser-71 is expressed in normal breast tissue cells but not in breast cancer cells
Cellular Localization
Nucleus. Nucleus speckle. Cytoplasm. Note=Co-localizes with NEK6 in the nucleus. Mainly localized in the nucleus but phosphorylation at Ser-71 by DAPK1 results in inhibition of its nuclear localization
A. Western blot analysis on HeLa cell lysates using anti-Phospho-Pin1 (pS16) RabMAb (Cat. #AJ1611b), 1:500 dilution. Cells were either (A) untreated or (B) treated with FBS + Calyculin A.
Application Notes
WB:1:500
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer
50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.