She Activators encompass a range of chemical compounds that facilitate the enhancement of She's functional role within cellular signaling pathways. For example, Forskolin, through its capacity to raise intracellular cAMP levels, indirectly encourages She's activity by promoting PKA-related phosphorylation events that She is implicated in. PMA, by activating PKC, might phosphorylate proteins that interact with She, thus strengthening its involvement in growth and differentiation signals. Similarly, Ionomycin and A23187, both calcium ionophores, elevate intracellular calcium levels, which can activate calcium-sensitive signaling molecules that enhance She's activity in these pathways. Sphingosine-1-phosphate, by engaging its G protein-coupled receptors, could initiate She activation in pathways pertinent to cell movement and vascular development.
Further, compounds like LY294002 and U0126, which inhibit PI3K and MEK1/2 respectively, can reduce Akt and ERK pathway activity, thereby relieving inhibitory feedback on pathways where She is active, leading to its enhanced functional role. SB203580's selective inhibition of p38 MAPK could similarly shift signaling dynamics to favor She activation in response to cellular stress. Thapsigargin, by disrupting calcium homeostasis, can indirectly potentiate She's involvement in calcium-dependent signaling.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine is a broad spectrum protein kinase inhibitor that can lead to selective activation of She by inhibiting kinases that normally suppress She’s involvement in particular signaling pathways. | ||||||