| Pcs | Single Vial, Pack of 10 |
|---|---|
| Strength | 10mg, 15mg, 30mg |
GLP-2T
$89.00 – $1,620.00Price range: $89.00 through $1,620.00
VERIFICATION
Every result against its specification.
How to read this report
GLP-2T, in structural terms.
- Sequence
- GLP-2T is a 39-residue acylated analogue built on the human gastric inhibitory polypeptide (GIP) backbone. The native reference sequence, GIP(1-42), is: Tyr-Ala-Glu-Gly-Thr-Phe-Ile-Ser-Asp-Tyr-Ser-Ile-Ala-Met-Asp-Lys-Ile-His-Gln-Gln-Asp-Phe-Val-Asn-Trp-Leu-Leu-Ala-Gln-Lys-Gly-Lys-Lys-Asn-Asp-Trp-Lys-His-Asn-Ile-Thr-Gln One-letter representation: YAEGTFISDYSIAMDKIHQQDFVNWLLAQKGKKNDWKHNITQ The native peptide is 42 residues, corresponding to residues 52–93 of the human GIP precursor (UniProt P09681). The analogue supplied here is shorter at 39 residues and is C-terminally amidated. It carries alpha-aminoisobutyric acid at two positions in the N-terminal region, which resists dipeptidyl peptidase-4 cleavage, and a C20 diacid fatty-acid chain attached to a lysine through a gamma-glutamate unit and two AEEA spacers. Its receptor binding profile spans more than one class B receptor, which is the property that distinguishes it from single-receptor analogues of this family. Identity for each lot is confirmed by mass spectrometric match to the labelled compound and reported on the certificate of analysis published on this page.
- Molecular formula
- C₂₂₅H₃₆₀N₆₂O₈₅
- Molecular weight
- 4813.5 g/mol
- CAS number
- 2023788-19-2
- Structure type
- Linear peptide
- Primary molecular target
- Class B (secretin-family) G protein-coupled incretin receptorsReceptors in this family share a large extracellular domain that binds the C-terminal portion of the peptide ligand, while the N-terminal portion engages the transmembrane core to drive receptor activation. This two-domain binding model is established in the structural literature for the class.
- Physical form
- Lyophilized powder
- PubChem CID
- 166567236
GLP-2 continues to be evaluated for its relevance in experimental biology, particularly within studies involving incretin signaling, receptor-level interactions, and biochemical pathway analysis.The peptide is manufactured by solid-phase peptide synthesis.
Where GLP-2T appears in the literature.
- Published experimental use of class B incretin receptor ligands includes:
- Receptor binding and competition studies at recombinant receptors
- cAMP accumulation and β-arrestin recruitment assays
- Cryo-electron microscopy of peptide–receptor–G protein complexes
- Receptor selectivity profiling across related class B receptors
- Biased signalling and receptor internalisation studies
- Analytical characterisation of synthetic peptide analogues by HPLC and high-resolution mass spectrometry
- These areas describe experimental research contexts and do not establish therapeutic efficacy or safety in humans.
- Experimental systems reported in this literature include:
- HEK293 and CHO cell lines stably expressing recombinant class B receptors
- Purified receptor–G protein complexes for structural determination
- Membrane preparations for radioligand binding
- Cell-free biophysical systems for peptide conformational study
- Isolated cell models used in published receptor pharmacology
- Assay formats reported in this literature include:
- Competition radioligand and fluorescent ligand binding assays
- HTRF and BRET cAMP accumulation assays
- β-arrestin recruitment and receptor internalisation assays
- Single-particle cryo-EM structure determination
- Reversed-phase HPLC with UV and mass spectrometric detection
- Circular dichroism for secondary structure assessment
- Endpoints reported in published research on this receptor class include:
- Binding affinity (Ki) and functional potency (EC50)
- Receptor selectivity ratios across related class B receptors
- cAMP accumulation and β-arrestin recruitment relative to reference ligand
- Receptor–ligand complex resolution and modelled contacts
- Chromatographic purity and mass accuracy for synthetic preparations
- Research use only. Not for human or animal consumption.
What has been studied, and in what systems.
In preclinical and laboratory research models, GLP-2T has been examined across hormonal, cellular, and molecular research systems. Research focus includes:
GLP-1 receptor signaling pathways
GIP receptor interaction models
Dual incretin receptor activity
Cellular signaling mechanisms
These observations are limited to controlled experimental environments and support ongoing laboratory investigations.
These are published research systems. They do not describe approved clinical applications, and they do not establish efficacy or safety in humans.
Brubaker PL et al., 2002. Structure-function of the glucagon receptor family of G protein-coupled receptors: the glucagon, GIP, GLP-1, and GLP-2 receptors. Recept Channels. PMID 12529935. https://pubmed.ncbi.nlm.nih.gov/12529935/
Novikoff A et al., 2021. Spatiotemporal GLP-1 and GIP receptor signaling and trafficking/recycling dynamics induced by selected receptor mono- and dual-agonists. Mol Metab. PMID 33556643. https://pubmed.ncbi.nlm.nih.gov/33556643/
Dinsmore I et al., 2024. Potent and Protease Resistant Azapeptide Agonists of the GLP-1 and GIP Receptors. Angew Chem Int Ed Engl. PMID 39151024. https://pubmed.ncbi.nlm.nih.gov/39151024/
About this compound and its batch data.
What purity did this GLP-2 batch achieve?
Lot 2026/02 was analysed by Krause Analytical and returned chromatographic purity of >99.9 % by HPLC with UV detection coupled to mass spectrometry. Identity was confirmed by mass spectral match. The full certificate is published on this page, and every figure shown here is taken from it.
How much GLP-2 is in the vial?
The laboratory measured 8.65 mg, which is 86.5% of the label claim. Net content is reported on a per-vial basis. Astramide publishes the measured figure rather than the label claim, whether it falls above or below.
Was this GLP-2 batch tested for endotoxins?
Yes. Endotoxin testing was performed using the Limulus Amebocyte Lysate assay in accordance with USP <85>, and this batch returned <0.5 EU/mL. The result appears on the certificate published on this page.
How should GLP-2 be stored for research use?
As supplied, the lyophilized powder should be held at -20°C and protected from light and moisture. Once reconstituted, store at 2-8°C and use within 14 to 30 days. Avoid repeated freeze-thaw cycles and follow the handling procedures appropriate to your laboratory.
What is the difference between research-grade and pharmaceutical-grade GLP-2?
These are separate classifications. Research-grade material is supplied for laboratory research use only and is not intended for human or animal consumption. Pharmaceutical-grade is an FDA classification that applies to drugs manufactured for human use. Astramide supplies research-grade material only.
How can I verify this GLP-2 certificate independently?
The certificate was issued by Krause Analytical under lot 2026/02, laboratory reference 205082. Quote that reference to the laboratory directly. The same document is published here in full, and is not summarised or reformatted by Astramide.
This product is intended strictly for in-vitro laboratory research conducted by qualified professionals. It is not intended for human or animal consumption, clinical use, or therapeutic application. The statements on this page have not been reviewed by the FDA. These research peptides are not intended to diagnose, treat, cure, or prevent any disease. Research Use Only.
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