is a powerful and competitive antagonist of cAMP-induced activation of cAMP-dependent protein kinase (PKA) I and II. Acting
8-Bromo-cAMP sodium saltTargetMol美国生化试剂,可用于动物细胞实验Product IntroductionBioactivity英文名: 8-Bromo-cAMP sodium salt描述
8-pCPT-2-O-Me-cAMP-AMTargetMol美国生化试剂,可用于动物细胞实验Product IntroductionBioactivity英文名: 8-pCPT-2-O-Me-cAMP-AM描述: Epac
Bucladesine | MedChemExpress (MCE)MedChemExpress (MCE)美国Bucladesine (Dibutyryl cAMP; DBcAMP) 是一种膜渗透性选择性激活剂,能够激活环磷酸腺苷
Bucladesine sodiumMedChemExpress (MCE)美国Bucladesine sodium salt (Dibutyryl-cAMP sodium salt) 是一种稳定的环 AMP (cAMP) 类似物,也是
HJC0197MedChemExpress (MCE)美国HJC0197 是一种有效的 Epac1 (cAMP 1 直接激活的交换蛋白) 和 Epac2 (对 Epac2 的 IC50=5.9 μM) 拮抗剂。HJC0197 选择性阻断
, Mouse, Recombinant (His)描述: PRKAR1A, also known as PRKAR1 and PKR1, is one of the regulatory subunits of cAMP
Adenosine 3′,5′-cyclic monophosphate上海阿拉丁生化科技股份有限公司阿拉丁中国产品介绍:cAMP依赖的蛋白激酶(PKA)的激动剂。cAMP是许多系统至神经递质或荷尔蒙诱导的受体刺激的第二信使, cAMP
′,5′-cyclic monophosphate (cAMP) is an activator of cyclic-AMP-dependent protein kinase A (PKA). The cAMP/PKA signaling
messenger cAMP from ATP. Its transcript is probably degraded by endoribonuclease LS (rnlA), decreasing cAMP levels
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