p27 Background Information Cell cycle progression is regulated by a series of cyclin-dependent kinases consisting of catalytic subunits, designated Cdks, as well as activating subunits, designated cyclins. Orderly progression through the cell cycle requires the activation and inactivation of different cyclin-Cdks at appropriate times. A series of proteins has recently been described that function as “mitotic inhibitors.” These include p21, the levels of which are elevated upon DNA damage in G1 in a p53-dependent manner; p16; and a more recently described p16-related inhibitor designated p15. A p21-related protein, p27, has been described as a negative regulator of G1 progression and speculated to function as a possible mediator of TGF∫-induced G1 arrest. p27 interacts strongly with D-type cyclins and Cdk4 in vitro and, to a lesser extent, with cyclin E and Cdk2.
p27 (SX53G8.5)
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p27 (SX53G8.5): sc-53871. Western blot analysis of p27 expression in SK-BR-3 (A), MDA-MB-231 (B) and MCF7 (C) whole cell lysates.
p27 (SX53G8.5): sc-53871. Western blot analysis of p27 expression in non-transfected: sc-110760 (A) and human p27 transfected: sc-110470 (B) 293 whole cell lysates.
p27 (SX53G8.5): sc-53871. Western blot analysis of p27 expression in non-transfected 293T: sc-117752 (A), mouse p27 transfected 293T: sc-122312 (B) and Jurkat (C) whole cell lysates.