> Semaglutide 10 mg · Lumera Labs
For laboratory research use only. Not for human consumption. Free cold-chain shipping over $110 CAD · Ships from Kelowna, BC
Free cold-chain shipping over $200 CAD · Ships from Kelowna, BC
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Semaglutide 10 mg vial
4.6 · 209 researcher reviews
GLP-1 · Metabolic Axis

Semaglutide

SKU LUM-SEMA-5 · C₁₈₇H₂₉₁N₄₅O₅₉ · 4113.58 g/mol · CAS 910463-68-2

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.

Purity (HPLC)
≥ 99.41%
Net peptide
5.00 mg ± 2%
Endotoxin
< 0.5 EU/mg
Format
Lyophilized vial
Storage
−20 °C, desiccated
Shelf life
24 months from MFG
$110CAD / 10 mg vial
In stock · Lot 26-A031
Qty
Bulk 10+: $24 / vial
Add $200 for free cold-chain shipping
  • HPLC + MS verified per lot
  • Cold-chain to your door
  • COA bundled with shipment
  • Lot retains kept 5 years

Overview

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.

Research applications

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.

Identity

ParameterValue
Molecular formulaC₁₈₇H₂₉₁N₄₅O₅₉
Molecular weight4113.58 g/mol
CAS number910463-68-2
Sequence length31 residues
Modificationγ-Glu-C18 diacid at Lys26

Quality

TestSpecification
HPLC purity≥ 99.0% (lot 26-A031: 99.41%)
Mass confirmationESI-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%

Lot 26-A031

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.

Verification

MethodResult
RP-HPLC at 220 nm99.41% main peak
ESI-MS (positive)4113.6 Da (theor. 4113.58)
Amino acid analysis82.1% net peptide
LAL endotoxin< 0.05 EU/mg
Karl Fischer (water)2.8% w/w

Reconstitution

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.

Storage after reconstitution

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.

Selected references

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.

Citing this material

Semaglutide reference standard, ≥99% (HPLC), Lumera Labs Inc., Cat. No. LUM-SEMA-5, Lot 26-A031.

Related · Metabolic axis

Often paired in studies.

View catalog

Why Lumera

  • Janoshik Analytical HPLC ≥ 99.41% on this lot
  • LC-MS identity confirmed before release
  • LAL endotoxin below detection limit
  • Cold-chain shipped −20°C from Kelowna, BC
Background research

What the literature says about Semaglutide.

Mechanism

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.

Common research applications

  • In-vitro receptor-binding and dose-response screens against the incretin signaling target panel.
  • Comparative pharmacology against related class members and previously published reference standards.
  • Time-course studies leveraging Semaglutide's known stability profile.
  • Cross-batch HPLC fingerprint comparison against the lot-specific COA we publish for every release.

Storage & handling

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.

References

  1. Lau J et al. J Med Chem. 2015;58(18):7370-80.
  2. Marso SP et al. N Engl J Med. 2016;375(19):1834-44.
  3. Knudsen LB. Front Endocrinol. 2019;10:155.

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.

$110 CAD