Date published: 2025-9-12

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FAM221B Activators

Forskolin, a well-known adenylate cyclase activator, effectively increases intracellular cAMP levels, which in turn can activate protein kinase A (PKA). The activation of PKA is a pivotal step in the phosphorylation of numerous target proteins, which can result in altered protein function and activity. AICAR, through its activation of AMP-activated protein kinase (AMPK), plays a crucial role in cellular energy homeostasis, influencing various aspects of protein activity and cellular metabolism. In the context of intracellular signaling, Lithium chloride emerges as an inhibitor of glycogen synthase kinase-3 beta (GSK-3β), thereby potentially activating proteins involved in the Wnt signaling pathway, a pathway integral to cell proliferation and differentiation. Trichostatin A and 5-Azacytidine, by modulating chromatin structure and DNA methylation respectively, exert profound effects on gene expression and, consequently, protein synthesis and activity. Additionally, the proteasome inhibitor MG132 prevents the degradation of proteins, which could lead to the stabilization and accumulation of target proteins, including FAM221B.

Further along the spectrum of cellular signaling modulation, Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), a kinase that regulates a multitude of cellular functions, including cell growth and apoptosis. SB431542 acts on the transforming growth factor-beta (TGF-β) signaling pathway by inhibiting the ALK5 kinase, affecting the SMAD signaling cascade. Y-27632, by inhibiting Rho-associated kinase (ROCK), can impact cytoskeletal dynamics, which is closely linked to the regulation of protein activity. JNK inhibitors like SP600125 influence the activity of transcription factor AP-1, further affecting protein function. PI3K and mTOR are central nodes in cell survival and metabolism signaling networks, with LY294002 inhibiting PI3K and Rapamycin targeting mTOR, each leading to a cascade of effects on downstream protein activities.

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