Chemical activators of Olfr474 can efficiently trigger its functional activation through various mechanisms. Forskolin, a well-known activator, initiates the process by elevating intracellular cyclic adenosine monophosphate (cAMP) levels. This surge in cAMP serves as a critical signal for Olfr474 activation, ultimately leading to the activation of protein kinase A (PKA) and subsequent gene function. Isoproterenol plays a significant role in stimulating Olfr474 via beta-adrenergic receptors. Activation of these receptors sets off a series of intracellular events that activate downstream signaling pathways, resulting in the functional activation of Olfr474. 8-Br-cAMP, another chemical activator, effectively mimics the action of cAMP, which is pivotal in promoting protein kinase A (PKA) activity. This activation of PKA serves as a key factor in Olfr474's functional enhancement. Phorbol 12-myristate and TPA (12-O-Tetradecanoyl-dibutyrate) activate Olfr474 by stimulating protein kinase C (PKC), which, in turn, leads to the phosphorylation of target proteins, thereby increasing the gene's functional activity. Capsaicin engages transient receptor potential channels, facilitating calcium influx and resulting in the functional activation of Olfr474. Retinoic acid binds directly to Olfr474's nuclear receptor, enhancing transcription and ultimately gene function.
Ionomycin and A23187 both induce Olfr474 activation by facilitating calcium ionophore-mediated calcium influx, which in turn triggers downstream signaling cascades and functional gene activation. 8-pCPT-2'-O-Me-cAMP acts as a cAMP analog, effectively mimicking cAMP's action, leading to increased PKA activity and gene functional enhancement. Bay K 8644 modulates calcium channel activity, resulting in enhanced calcium influx and functional gene activation. Retinol, a precursor to retinoic acid, enhances Olfr474 function by binding to its nuclear receptor, subsequently activating gene function. These chemical activators collectively contribute to the efficient functional activation of Olfr474 through diverse pathways, enabling precise control of its activity.
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