P1-2 TZ
P1-2 TZ / 30 MG1 / 3A dual-receptor peptide studied for activity across GLP-1 and GIP pathways, used in research on incretin-mediated metabolic and endocrine signaling. Its dual-agonist mechanism allows researchers to investigate how combined incretin receptor activation influences glucose homeostasis and metabolic coordination.
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Lot P1P-TZ30-001 · Janoshik
For laboratory research only. Not for human or veterinary use.
About P1-2 TZ
P1-2 TZ Overview
P1-2 TZ is a dual-receptor peptide studied for activity across GIP and GLP-1 pathways. In research settings, it is used to examine how these two receptor systems work together and how combined receptor activity influences broader metabolic and endocrine signaling. P1-2 TZ has been described in the literature as an acylated peptide engineered to activate both the GIP and GLP-1 receptors.
Mechanism of Action & Applications
P1-2 TZ is studied as a dual agonist at the GIP and GLP-1 receptors. This receptor profile allows researchers to examine how simultaneous activation of incretin-related pathways affects intracellular signaling, hormone pathway coordination, and broader metabolic system responses. Published mechanistic work also describes P1-2 TZ as having stronger relative activity at the GIP receptor and biased signaling behavior at the GLP-1 receptor, which makes it a useful compound for studying receptor-selective signaling and dual-incretin pathway biology. It is commonly used in research involving incretin receptor biology, metabolic signaling, endocrine regulation, and multi-pathway peptide signaling.
Research History
P1-2 TZ builds on earlier incretin research that first focused on GLP-1 receptor agonists and later expanded into compounds designed to engage both GIP and GLP-1 receptors. This progression led to dual-agonist peptides like P1-2 TZ, which are studied for more integrated pathway research involving incretin signaling and metabolic system coordination.
Chemical Information
- CAS Number
- 2023788-19-2
- Molecular Formula
- C225H348N48O68
- Molecular Weight
- 4,813.45 g/mol
- PubChem ID
- 166567236
The details.
- Compound
- P1-2 TZ
- Selected quantity
- 30 MG per vial
- Research area
- Metabolic & Endocrine
- Intended use
- Laboratory research only
Laboratory storage & handling
- Form
- Lyophilized powder
- Short-term
- 2–8 °C (refrigerated)
- Long-term
- −20 °C (frozen)
- Container
- Use the supplied container and follow its label
- Lot-specific stability
- Not established on this product page
- Reconstitution
- Consult the applicable research protocol and available lot record
For research use only. Not for human or veterinary use.
Detailed storage guidelinesKnow your record.
The certificate below belongs to P1-2 TZ 30 MG, lot P1P-TZ30-001. Match the lot number on your vial to the record.
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