DUAL GIP / GLP-1 AGONIST
In stock
GLP-2T pairs two of the body's incretin signals — GIP and GLP-1 — in a single peptide. Dual-target compounds like this sit at the center of modern metabolic research, and this is the reference version of the class in our catalog.
Researchers reach for it to see what two receptors do together that one can't do alone: how the signals overlap, where they differ, and how the combination shifts metabolic pathways in lab models.
Keep the sealed vials in the fridge and out of direct light — they’ll hold up for a long time that way. Once a vial is mixed, keep it refrigerated and use it within the window your protocol calls for.
Every batch we sell is tested by an independent U.S. lab before it goes up for sale — that report is the certificate of analysis, and a copy is included with every order. Want the one for your exact vial? Email the lot number printed on the label to [email protected] and we’ll send it over within one business day.
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Also referenced as: dual GIP/GLP-1 receptor agonist · twincretin
GLP-2T is a 39-amino-acid synthetic peptide built on a GIP backbone and tuned so it activates both the GIP receptor and the GLP-1 receptor — the two incretin signals the gut releases when food arrives. Compounds with this dual profile are sometimes called twincretins, and they sit at the center of modern metabolic pharmacology.
A fatty-diacid chain on the peptide binds serum albumin, protecting it from clearance and giving it a long duration of action. That engineering is what separates research-grade dual agonists from the native hormones, which survive only minutes in circulation.
The scientific question behind GLP-2T is crosstalk: what do GIP and GLP-1 signalling do together that neither does alone? Published work spans receptor-bias studies (the compound engages the GIP receptor with full potency and the GLP-1 receptor with deliberately imbalanced potency), insulin-secretion assays in islet preparations, and appetite and glucose models in rodents.
Because dual agonism outperformed single agonism in so much preclinical work, GLP-2T has become the class reference — the molecule newer multi-receptor designs are measured against. Labs building comparative studies usually anchor one arm with it.
Each vial is lyophilized powder, verified at 98.9% purity by HPLC with CAS-confirmed identity and endotoxin screening below 0.5 EU/mg. Store lyophilized at −20 °C away from light; reconstituted material belongs at 2–8 °C and should be used within your protocol's window.
For ladder or comparison designs, our GLP-1 vial covers the single-agonist arm and GLP-3R the triple-agonist arm, all tested to the same standard.
The published record runs deeper than any product page should. For the primary literature, browse GLP-2T studies on PubMed. For how every batch we sell is verified, see how we test.
From our research library: The incretin ladder: one, two, three receptors.
No. GLP-2T is supplied strictly for laboratory research. It is not for human or veterinary use, and every order requires agreement to our research-use policy.
One peptide, two receptors. GLP-2T binds and activates both the GIP receptor and the GLP-1 receptor, so a single compound can probe how the two incretin pathways interact — something you can't cleanly do by co-dosing two separate peptides with different half-lives.
For years GIP was the overlooked incretin. Dual-agonist studies revived it: preclinical work suggests GIP-receptor activity shapes insulin response and adipose-tissue signalling in ways that complement GLP-1 activity, and much of the current literature is untangling that contribution.
The current batch is 98.9% pure by HPLC, tested by an independent US laboratory before sale — along with identity confirmation and endotoxin screening below 0.5 EU/mg. The certificate of analysis is included with every order, and the report for any specific vial is available by emailing its lot number.
GLP-2T is available in 10mg, 20mg, 30mg and 50mg vials of lyophilized powder. Quantity discounts apply automatically at checkout.
Keep sealed vials frozen at −20 °C and away from light. Once reconstituted, hold the solution at 2–8 °C and use it within the window your laboratory protocol defines.
