For in vitro research use only. For research and identification purposes only. Not for human or veterinary use; not a food, cosmetic, or drug product.
In stock
For In Vitro Research Use Only
Not for Human or Veterinary Application
Survodutide is a synthetic acylated peptide that acts as a dual agonist at the glucagon receptor (GCGR) and the GLP-1 receptor (GLP-1R). It is used as a research tool for studying dual glucagon and GLP-1 receptor activation in cell-based models.
Quantity: 10 mg
Form: Lyophilized Powder
Molecular Formula: C192H289N47O61
CAS: 2805997-46-8
Molecular Weight: 4,231.6 Da
Purity: Printed on the lot certificate
Storage: -20°C long-term; 4°C short-term (use within 4 weeks of reconstitution)
Every lot is tested by an independent laboratory. The certificate for this product is shown on this page and on the Test Results page.
This compound is intended strictly for in vitro laboratory research by qualified professionals. It is not a drug, food, or cosmetic and is not approved for:
Human use
Veterinary use
Food, drug, diagnostic, or cosmetic applications
This compound has not been evaluated by the U.S. Food and Drug Administration (FDA). It is not intended to diagnose, treat, cure, or prevent any disease.
It is sold strictly as a research material with no medical or therapeutic claims.
All handling and use must comply with applicable institutional, local, state, and federal regulations.
By purchasing from Axis Peptide Labs, the buyer confirms that they are a qualified researcher, laboratory, or institution and acknowledge that the product is for research use only.
The purchaser assumes full responsibility for compliant handling, storage, and use.
Resale for human consumption is strictly prohibited.
Research Use Only
Axis Peptide Labs sells research peptides exclusively to qualified researchers and laboratories for in vitro and laboratory use. Please confirm before continuing.
By proceeding you affirm the statements above are true. Products are not for human or veterinary use, not for use in diagnostic procedures, and have not been evaluated by the U.S. Food and Drug Administration.
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