99.84%View COAGLP2-TZ
Dual GIP / GLP-1 receptor agonist for incretin-signalling research.

Long-acting GLP-1 receptor agonist analogue for metabolic pathway studies.
RFID on the vial. Hold it to the back of your phone and its certificate of analysis opens automatically.
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Long-acting GLP-1 receptor agonist analogue for metabolic pathway studies.
20 mg per vial, as a lyophilized powder in a sealed glass vial with a crimped cap. The lot number on the label matches the certificate of analysis in the COA library, and the RFID tag on the vial opens that certificate when you hold it to the back of your phone.
Store lyophilized powder frozen (−20 °C) or refrigerated, sealed and away from light. Once reconstituted, keep refrigerated (2–8 °C).
Handle in a laboratory setting using appropriate protective equipment. Consult the certificate of analysis and safety data for lot-specific information.
GLP1-SG is a long-acting analogue of glucagon-like peptide-1 (GLP-1), a 31-residue lipidated peptide that activates the GLP-1 receptor. It is supplied for laboratory research into incretin signalling, glucose-dependent insulin secretion and the central pathways that regulate appetite and energy balance.
GLP-1 is an incretin hormone released by enteroendocrine L-cells of the intestine after a meal. Through the GLP-1 receptor, a class B G protein-coupled receptor, it amplifies insulin secretion when glucose is elevated, restrains glucagon release, slows gastric emptying and signals satiety in the brain1,2.
Native GLP-1 is cleared within minutes because dipeptidyl peptidase-4 (DPP-4) cleaves its N-terminus and the kidney filters it rapidly. Long-acting analogues such as GLP1-SG are engineered to resist that: amino-acid substitutions protect the cleavage site, and an attached fatty-acid side chain lets the peptide bind serum albumin, which markedly protracts its action in pharmacokinetic studies2,3.
Because a long-acting analogue keeps the receptor engaged between administrations in study models, researchers can examine sustained receptor activation rather than the brief post-meal pulse of the native hormone. That has made the class a reference point for metabolic research and for newer multi-receptor compounds such as the dual GIP / GLP-1 agonist GLP2-TZ and the triple agonist GLP3-RT4.
Findings from receptor pharmacology, animal models and clinical studies of related medicines are not interchangeable: results depend on the exact molecule, the model and the study design. This research compound is not a medicine, has not been evaluated by the FDA, and is sold for laboratory research only.
They differ in how many receptors they act on. GLP1-SG is a GLP-1 receptor agonist; GLP2-TZ acts on both the GIP and GLP-1 receptors; GLP3-RT acts on the GLP-1, GIP and glucagon receptors.
Native GLP-1 is cleaved by DPP-4 and cleared within minutes. Long-acting analogues protect the cleavage site and carry a fatty-acid chain that binds albumin, which slows clearance2,3.
Sealed vials of lyophilized peptide are kept frozen (−20 °C) or refrigerated, dry and away from light. Peptide storage and stability explains why.
Every lot is tested by an independent laboratory for identity (mass spectrometry) and purity (HPLC). The certificate for the lot on your vial is published in the COA library and linked from this page.
Research summary reviewed 2026-10-26 against the cited literature.
99.84%View COADual GIP / GLP-1 receptor agonist for incretin-signalling research.
99.91%View COATriple-agonist peptide studied at the GLP-1, GIP and glucagon receptors.
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