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Injection · 10 mg · vial
Xeno Laboratories Tirzepatide is a 10 mg lyophilized vial of a synthetic peptide that signals through two incretin receptors, GIP and GLP-1, which makes it a research standard for dual-agonist work.
GMP-manufactured and HPLC-verified, with a Certificate of Analysis per batch, reconstituted with bacteriostatic water and shipped internationally and to the United States.
Xeno Laboratories Tirzepatide is a 10 mg lyophilized vial of a synthetic peptide built to activate both the GIP and the GLP-1 receptor, a design published as the reason its signalling profile differs from single-receptor incretin drugs. A 39-amino-acid backbone with a fatty-acid side chain is what the literature describes: the chain binds albumin and stretches the duration of action, while the backbone supplies dual affinity. In the laboratory it is read against a single-agonist comparator such as Semaglutide, because the pair isolates the second receptor contribution.
Receptor pharmacology is the core of the published mechanism: GIP and GLP-1 receptor engagement produce overlapping but non-identical downstream responses, and studies measure cyclic AMP accumulation and insulin release in cultured cell lines with the receptors expressed separately or together. Animal models in the literature add gastric emptying and food-intake endpoints. The point of a dual-agonist standard is comparison, so assay design runs a single-agonist arm in parallel rather than testing the peptide alone.
Bacteriostatic water is added down the wall of the vial and the solution is swirled, not shaken, because the peptide is a fragile chain that denatures when foamed. Concentration is milligrams divided by millilitres of diluent, so the unit value on a syringe depends on the volume chosen; the published conversions for a 10 mg vial are calibration examples for laboratory work, not amounts to take. Sealed powder stays cold and dry, and reconstituted solution belongs in a refrigerator with no repeated freeze-thaw cycling.
Tirzepatide is an approved prescription medicine in several markets under another trade name, so a large supervised human dataset exists, with gastrointestinal effects the most frequently reported in the label and pharmacovigilance reviews. That dataset belongs to the licensed product in clinical use. This vial is laboratory research material, is not a licensed medicine, and carries no dose, no schedule and no instruction for human use.
For laboratory research only. Not for human or veterinary use. Information provided is for educational purposes only and does not constitute medical advice. Consult a healthcare professional before use.
| Trade Name | Tirzepatide |
| Generic Name | Tirzepatide (dual GIP/GLP-1 agonist) |
| Manufacturer | Xeno Laboratories |
| Dosage | 10 mg per vial |
| Package | Lyophilized powder, one vial |
| Drug Class | Dual incretin agonist |
| Administration | Laboratory reference material, not for administration |
| Storage | Sealed powder cold and dry, solution 2 to 8 C |
| Prescription Status | Licensed medicine elsewhere; this vial is research material |
| Verification | HPLC per batch, COA on file |
| Shipping | International and U.S. domestic options |
For laboratory research only. Consult a healthcare professional before handling any peptide. Amounts shown are research references, not recommended human doses.
Before you ask
Tirzepatide is a synthetic peptide that activates two incretin receptors, GIP and GLP-1, rather than one. Its published design uses a long backbone with a fatty-acid side chain, and the side chain is what binds albumin and extends duration of action in the body. The dual affinity is why laboratory work treats it as a comparator for single-receptor agonists instead of as another version of them.
Semaglutide engages the GLP-1 receptor alone, while Tirzepatide engages the GIP receptor as well, so receptor panels and binding assays separate the two clearly. Downstream measurements such as cyclic AMP accumulation and insulin release overlap in part, which is exactly why a study runs both compounds in parallel arms rather than comparing published numbers from different laboratories and different assay conditions.
Add bacteriostatic water down the wall of the vial and swirl gently instead of shaking, since peptide solutions foam and lose structure under hard agitation. Concentration is milligrams divided by millilitres of diluent, so the unit value follows the volume chosen and the published conversion tables are calibration examples only. Store sealed powder cold and dry, and keep the mixed solution refrigerated without repeated freezing.
The molecule is licensed as a prescription medicine in several markets under another trade name, and the approved label lists gastrointestinal effects among the commonly reported ones that supervised use manages. This 10 mg vial is a separate product from the licensed medicine: it is sold as laboratory research material and carries no dosing instruction, no titration schedule and no guidance for human use.
Keep the sealed vial cold, dry and away from light, and let it reach room temperature before opening so condensation does not enter the powder. Once reconstituted, refrigerate the solution and avoid repeated freeze-thaw cycles, which are the usual route to a loss of potency. If a protocol needs several working sessions, split the solution into single-use aliquots before freezing.
The approved medicine label for this molecule lists gastrointestinal side effects as the most frequently reported, along with other warnings that prescribing clinicians monitor. That safety record belongs to supervised clinical use of the licensed product. Research material has no equivalent profile, since laboratory exposure data is not human safety data, and no dose or schedule appears on this page.
Yes, this 10 mg vial is listed with international checkout and a U.S. domestic shipping option, and every batch carries an HPLC report and a Certificate of Analysis. Orders are handled within one to two business days. Stock, pack and the current price are shown in the product block above, so check the availability line before ordering rather than assuming a dispatch time.
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