keep away from moisture
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Highly potent GIP receptor agonist (EC50 = 630 ± 119 pM). Displays equivalent cAMP stimulating properties and improved resistance to enzymatic degradation compared to native GIP in cells expressing wild type GIP receptor. Improves glucose tolerance, insulin release and cognitive function in various animal models of obesity and diabetes. Displays neuroprotective effects in an MPTP model of PD.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | 35 days | $ 1,180.00 |
Description | Highly potent GIP receptor agonist (EC50 = 630 ± 119 pM). Displays equivalent cAMP stimulating properties and improved resistance to enzymatic degradation compared to native GIP in cells expressing wild type GIP receptor. Improves glucose tolerance, insulin release and cognitive function in various animal models of obesity and diabetes. Displays neuroprotective effects in an MPTP model of PD. |
Molecular Weight | 4983.58 |
Formula | C226H338N60O66S |
CAS No. | 444073-04-5 |
keep away from moisture
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 1 mg/mL
You can also refer to dose conversion for different animals. More
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[D-Ala2]-GIP (human) 444073-04-5 [DAla2]GIP (human) [D-Ala2]-GIP [D Ala2] GIP (human) [D-Ala-2]-GIP (human) inhibitor inhibit