产品
编 号：F613603
分子式：C226H338N60O64S
分子量：4951.53
分子式：C226H338N60O64S
分子量：4951.53
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规格
价格
是否有货
结构图
CAS No: 299898-52-5
产品详情
生物活性：
(Pro3) GIP, human ((Pro3) Gastric Inhibitory Peptide, human) is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human has high binding affinity for human GIPR with Ki/ Kd values of 0.90 nM. (Pro3) GIP, human can be used for the research of obesity-related diabetes.
体内研究：
(Pro3) GIP, human has comparatively weak partial agonist effect in rodent models.
体外研究：
(Pro3) GIP, human induces cAMP accumulation with an EC50 value of 0.026 nM.(Pro3) GIP, human has high binding affinity for human GIPR, Rat GIPR and Mouse GIPR with Ki/ Kd values of 0.90 nM, 1.1 nM and 0.72 nM, respectively.
(Pro3) GIP, human ((Pro3) Gastric Inhibitory Peptide, human) is an efficacious, stable and specific human GIP receptor (hGIPR) full agonist. (Pro3) GIP, human has high binding affinity for human GIPR with Ki/ Kd values of 0.90 nM. (Pro3) GIP, human can be used for the research of obesity-related diabetes.
体内研究：
(Pro3) GIP, human has comparatively weak partial agonist effect in rodent models.
体外研究：
(Pro3) GIP, human induces cAMP accumulation with an EC50 value of 0.026 nM.(Pro3) GIP, human has high binding affinity for human GIPR, Rat GIPR and Mouse GIPR with Ki/ Kd values of 0.90 nM, 1.1 nM and 0.72 nM, respectively.
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