GIP(3-42)

≥98%

Reagent Code: #190953
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CAS Number 1802086-25-4

science Other reagents with same CAS 1802086-25-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 4749.9 g/mol
Formula C₂₁₄H₃₂₄N₅₈O₆₃S
inventory_2 Storage & Handling
Storage -20°C

description Product Description

GIP(3-42) is a truncated form of Glucose-dependent Insulinotropic Polypeptide (GIP), functioning primarily as a competitive antagonist or weak partial agonist at the GIP receptor. Its main application lies in research settings, particularly in studies related to glucose metabolism and insulin secretion. Scientists use GIP(3-42) to investigate the role of endogenous GIP by selectively blocking its receptor activity, helping to clarify the hormone’s contribution to the incretin effect. It is also employed in metabolic research to explore conditions such as type 2 diabetes and obesity. By inhibiting full-length GIP action, researchers can assess changes in insulin response, glucose tolerance, and energy balance. Additionally, GIP(3-42) supports studies examining the interaction between GIP and GLP-1 pathways, which is relevant for developing dual or multi-receptor agonist therapies for metabolic disorders. Due to its specific mode of action, it serves as a valuable tool for dissecting receptor-specific effects in cell cultures and animal models.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1mg
10-20 days ฿21,010.00
GIP(3-42)
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GIP(3-42) is a truncated form of Glucose-dependent Insulinotropic Polypeptide (GIP), functioning primarily as a competitive antagonist or weak partial agonist at the GIP receptor. Its main application lies in research settings, particularly in studies related to glucose metabolism and insulin secretion. Scientists use GIP(3-42) to investigate the role of endogenous GIP by selectively blocking its receptor activity, helping to clarify the hormone’s contribution to the incretin effect. It is also employed in metabolic research to explore conditions such as type 2 diabetes and obesity. By inhibiting full-length GIP action, researchers can assess changes in insulin response, glucose tolerance, and energy balance. Additionally, GIP(3-42) supports studies examining the interaction between GIP and GLP-1 pathways, which is relevant for developing dual or multi-receptor agonist therapies for metabolic disorders. Due to its specific mode of action, it serves as a valuable tool for dissecting receptor-specific effects in cell cultures and animal models.
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