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Adenosine triphosphate (ATP), a potassium efflux agent, can trigger the activation of NLRP3 inflammasome in response to PAMPs, such as LPS and peptidoglycan.It stimulates the caspase-1-dependent cle……
Adenosine triphosphate (ATP), a potassium efflux agent, can trigger the activation of NLRP3 inflammasome in response to PAMPs, such as LPS and peptidoglycan.
It stimulates the caspase-1-dependent cleavage and secretion of IL-1β from LPS-stimulated cells.
Working concentration: 5 mM
CAS number: 987-65-5
Molecular Weight: 551.14
Formula: C10H14N5O13P3 .2Na
Purity: ≥99.0% (HPLC)
Solubility: 400 mg/ml (725 mM) in water
1g ATP (adenosine 5’-triphosphate disodium salt) provided lyophilized
ATP is shipped at room temperature.
Store at -20°C.
Adenosine triphosphate (ATP), a potassium efflux agent, can trigger the activation of NALP3 inflammasome in response to PAMPs, such as LPS and peptidoglycan.
It stimulates the caspase-1-dependent cleavage and secretion of IL-1β from LPS-stimulated cells [1].
ATP triggers the opening of the non- selective cation channel of the purinergic P2X7 receptor, followed by the gradual opening of a larger pore.
The larger pore is attributed to pannexin-1, which is recruited upon P2X7 receptor activation [2].
Activation of the P2X7 receptor results in potassium efflux which is necessary for activation of the post- translational maturation of IL-1β [3].
References:
1. Mariathasan S. et al., 2006. Cryopyrin activates the inflammasome and ATP. Nature 440;228-32.
2. Locovei S. et al., 2007. Pannexin1 is part of the pore forming unit of the P2X(7) receptor death complex. FEBS Lett. 581(3):483-8.
3. Perregaux d. & Gabel ca., 1994. Interleukin-1β maturation and release in response to ATP and nigericin. J Biol. Chem. 269:15195-15203.
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