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A 31-residue GLP-1 receptor agonist with a fatty-acid side chain at Lys26 for albumin-mediated half-life extension. Lyophilized from acetate buffer; reconstitute with bacteriostatic water for in-vitro receptor assays.
Semaglutide is a long-acting glucagon-like peptide-1 receptor agonist used as a reference standard in metabolic and incretin-axis research. The C18 fatty diacid attached at Lys26 binds serum albumin reversibly, conferring a 165-hour effective half-life in mammalian models and reducing assay-to-assay drift in time-course studies.
Each vial is lyophilized from acetate-buffered solution at pH 4.0, sealed under nitrogen, and held at −20 °C through ship. Cold-chain insulation is maintained from our Kelowna facility to your bench.
In-vitro GLP-1R potency assays, β-arrestin recruitment screens, comparative pharmacokinetics versus exenatide and liraglutide, and structural studies of receptor-bound conformations. Compatible with HEK293, CHO, and INS-1E cell lines.
Sold for laboratory research only. This material is not a drug, food, or cosmetic and is not intended for diagnostic, therapeutic, or recreational use.
| Parameter | Value |
|---|---|
| Molecular formula | C₁₈₇H₂₉₁N₄₅O₅₉ |
| Molecular weight | 4113.58 g/mol |
| CAS number | 910463-68-2 |
| Sequence length | 31 residues |
| Modification | γ-Glu-C18 diacid at Lys26 |
| Test | Specification |
|---|---|
| HPLC purity | ≥ 99.0% (lot 26-A031: 99.41%) |
| Mass confirmation | ESI-MS within 0.5 Da |
| Net peptide content | ≥ 80% by AAA |
| Endotoxin | < 0.5 EU/mg (LAL) |
| Bioburden | < 10 CFU/g |
| Residual TFA | < 1.0% |
Manufactured 04 Mar 2026 · Released 11 Mar 2026 · Tested by Lumera QC, Kelowna BC. Retain samples held under storage spec for five years from release date.
| Method | Result |
|---|---|
| RP-HPLC at 220 nm | 99.41% main peak |
| ESI-MS (positive) | 4113.6 Da (theor. 4113.58) |
| Amino acid analysis | 82.1% net peptide |
| LAL endotoxin | < 0.05 EU/mg |
| Karl Fischer (water) | 2.8% w/w |
Allow vial to reach room temperature before opening (≥ 20 minutes). Reconstitute with 1.0–2.5 mL of sterile bacteriostatic water (0.9% benzyl alcohol). Inject solvent slowly down the inner wall of the vial; do not direct stream onto the lyophilized cake.
Swirl gently for 30 seconds. Do not vortex. Allow to dissolve for 5 minutes; clarity should be complete with no visible particulates.
Reconstituted solution is stable for 28 days at 2–8 °C in original vial. For longer storage, aliquot into low-binding tubes and hold at −80 °C; avoid repeated freeze-thaw cycles. Discard if turbidity, color change, or particulate matter is observed.
Knudsen LB, Lau J. The discovery and development of liraglutide and semaglutide. Front Endocrinol. 2019;10:155.
Lau J et al. Discovery of the once-weekly GLP-1 analogue semaglutide. J Med Chem. 2015;58(18):7370–80.
Semaglutide reference standard, ≥99% (HPLC), Lumera Labs Inc., Cat. No. LUM-SEMA-5, Lot 26-A031.
Semaglutide is a long-acting GLP-1 analog, classified within the incretin signaling pathway. Structurally it is a C20 fatty-diacid GLP-1R agonist. Semaglutide is a 31-residue analog of human glucagon-like peptide-1 (GLP-1) bearing a C18 diacid attachment via a γ-glutamyl spacer at Lys26. Lau et al. (2015) reported its discovery and characterized its sub-nanomolar GLP-1R potency and extended functional half-life. Marso et al. (2016) followed with the SUSTAIN-6 cardiovascular outcomes data.
In an in-vitro setting, Semaglutide interacts with its target receptor(s) at low-nanomolar affinities under standard binding-assay conditions. Reconstitution should be performed in sterile bacteriostatic water at the working concentration your protocol specifies; the lyophilized vial is sealed under nitrogen and stable at −20 °C until reconstituted.
Semaglutide arrives lyophilized at −20 °C in cold-chain insulated packaging. On receipt, transfer immediately to a −20 °C freezer. Once reconstituted, store at 2-8 °C and use within the window noted on the lot's COA. Avoid repeated freeze-thaw cycles.
For laboratory research only. Semaglutide is sold strictly as an in-vitro reference standard. It is not approved for human or veterinary use by Health Canada or the FDA.