[Pro3]-GIP (Rat)

• Description :

  High affinity rat GIP receptor partial agonist (Kd = 13 nM) . Increases cAMP accumulation in COS-7 cells transfected with rat GIP receptor, while also acting as a competitive antagonist of GIP.

• Stability :

  ≥ 2 years

• Purity :

  >98% (HPLC)

• Weight :

  4970.63

• Molecular Formula :

  C226H343N61O64S

• Notes :

  Research use only, not for human use.

• Receptor :

  ——