"1700016L21Rik" Activators comprise a series of chemical compounds that are designed to enhance the functionality of the "1700016L21Rik" protein through various biochemical pathways. Forskolin, Isoproterenol, 8-Br-cAMP, db-cAMP, and Rolipram are all agents that increase intracellular cAMP levels, which subsequently activate protein kinase A (PKA). PKA is known to phosphorylate a myriad of proteins, potentially including "1700016L21Rik", thus augmenting its activity within cAMP-dependent signaling processes. Ionomycin and A23187, both calcium ionophores, and Bay K8644, an L-type calcium channel agonist, elevate intracellular calcium concentrations. This rise in calcium may activate calcium/calmodulin-dependent protein kinases, which could subsequently enhance the activity of "1700016L21Rik" if it is a part of or regulated by calcium-dependent signaling mechanisms. The activation by these compounds suggests a role for "1700016L21Rik" in pathways sensitive to fluctuations in cAMP or intracellular calcium levels.
Moreover, Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which is integral to numerous signaling cascades and could enhance "1700016L21Rik" activity if it is a PKC substrate or involved in PKC-mediated pathways. S-Nitroso-N-acetylpenicillamine (SNAP) and Zaprinast work by increasing cellular levels of cGMP, a secondary messenger that activates protein kinases like PKG. If "1700016L21Rik" is part of the cGMP-dependent signaling pathways, its activity would be enhanced by these compounds. IBMX, a non-specific phosphodiesterase inhibitor, raises levels of both cAMP and cGMP, suggesting a potential broad activation of "1700016L21Rik" across multiple cyclic nucleotide-dependent pathways. Collectively, these activators suggest that "1700016L21Rik" operates within a network of signaling pathways regulated by cyclic nucleotides and calcium, and its activation is crucial for the proper functioning of these pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $78.00 $270.00 | 80 | |
Ionomycin acts as a calcium ionophore, elevating intracellular calcium levels. This triggers calcium-dependent protein kinases, potentially enhancing the activity of "1700016L21Rik" if it is regulated by calcium-sensitive pathways. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $28.00 $38.00 | 5 | |
Isoproterenol is a β-adrenergic agonist that increases intracellular cAMP levels, similar to forskolin, thus activating PKA. PKA may then phosphorylate and enhance "1700016L21Rik" within the relevant signaling pathways. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $41.00 $132.00 $214.00 $500.00 $948.00 | 119 | |
PMA activates protein kinase C (PKC), which can phosphorylate a variety of proteins. If "1700016L21Rik" is a substrate or is regulated by PKC-mediated pathways, this would lead to its activation. | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $55.00 $131.00 $203.00 $317.00 | 23 | |
A23187 is a calcium ionophore that increases intracellular calcium, similar to ionomycin. This could enhance "1700016L21Rik" by activating calcium/calmodulin-dependent protein kinases if "1700016L21Rik" is influenced by calcium signaling. | ||||||
8-Bromoadenosine 3′,5′-cyclic monophosphate | 23583-48-4 | sc-217493B sc-217493 sc-217493A sc-217493C sc-217493D | 25 mg 50 mg 100 mg 250 mg 500 mg | $108.00 $169.00 $295.00 $561.00 $835.00 | 2 | |
8-Br-cAMP is a cAMP analog that activates PKA. By activating PKA, it can enhance the activity of "1700016L21Rik" if it is involved in cAMP-responsive pathways. | ||||||
Dibutyryl-cAMP | 16980-89-5 | sc-201567 sc-201567A sc-201567B sc-201567C | 20 mg 100 mg 500 mg 10 g | $47.00 $136.00 $492.00 $4552.00 | 74 | |
db-cAMP is another cAMP analog that activates PKA and can enhance the activity of "1700016L21Rik" by promoting its function in cAMP-dependent signaling cascades. | ||||||
(±)-Bay K 8644 | 71145-03-4 | sc-203324 sc-203324A sc-203324B | 1 mg 5 mg 50 mg | $84.00 $196.00 $817.00 | ||
Bay K8644 acts as an L-type calcium channel agonist, enhancing calcium influx and potentially increasing the activity of "1700016L21Rik" through calcium-dependent signaling pathways. | ||||||
Zaprinast (M&B 22948) | 37762-06-4 | sc-201206 sc-201206A | 25 mg 100 mg | $105.00 $250.00 | 8 | |
Zaprinast inhibits phosphodiesterase 5 (PDE5), leading to increased cGMP levels, which may enhance "1700016L21Rik" activity if it operates within cGMP-dependent signaling mechanisms. | ||||||
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $260.00 $350.00 $500.00 | 34 | |
IBMX is a non-specific inhibitor of phosphodiesterases, increasing both cAMP and cGMP levels. This could enhance "1700016L21Rik" activity by affecting various cyclic nucleotide-dependent pathways. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $77.00 $216.00 | 18 | |
Rolipram is a selective inhibitor of PDE4, which specifically increases cAMP levels. By elevating cAMP, it can enhance "1700016L21Rik" activity in pathways that are responsive to cAMP-mediated signaling. | ||||||