GLP-3 is a triple-agonist analogue referenced in scientific literature for its role in studying GLP-1, GIP, and glucagon receptor pathways. It is frequently used in research models examining multi-receptor engagement, intracellular cAMP-related signaling, and peptide structure–function relationships. Each vial is provided as a lyophilized peptide and undergoes third-party analytical verification to confirm identity and purity for laboratory research use.
GLP-3 is a synthetic multi-agonist peptide frequently referenced in scientific literature for its relevance in studies involving GLP-1, GIP, and glucagon receptor pathways. Researchers commonly examine GLP-3 within models evaluating multi-receptor engagement, intracellular cAMP-associated signaling, and molecular mechanisms related to metabolic pathway mapping and endocrine-related biochemical cascades.
In published scientific contexts, GLP-3 is often discussed in investigations assessing its interaction across multiple incretin-related receptor families, its structural modifications designed to influence peptide stability, and its involvement in studies exploring receptor-selective biochemical signaling networks. Due to its recurring presence in these research domains, GLP-3 is widely utilized in laboratory environments focused on peptide structure–function characterization, receptor-binding analysis, and multi-pathway endocrine signaling models.
This research material is supplied as a lyophilized peptide and undergoes third-party analytical verification to confirm identity and purity before distribution.
Molecular Weight: ~4800–5000 g/mol (approx., depending on reference sequence)
Storage: Store in a cool, dry environment away from direct light
Intended Use: Laboratory research and analytical reference only
Commitment to Analytical Verification
At BioFusion Peptides, every compound is supported by formal analytical documentation to validate composition, quality, and consistency. Certificates of Analysis serve as a cornerstone of our quality framework, providing objective data derived from standardized laboratory testing.
Each certificate reflects method-driven evaluation performed using industry-recognized analytical techniques, ensuring materials meet clearly defined specifications before release.
What Our Documentation Confirms
Compound Authentication Advanced analytical methods are used to verify molecular structure and confirm alignment with the intended reference profile.
Compositional Integrity Chromatographic analysis establishes the relative abundance of the primary compound and quantifies the presence of secondary components.
Verified Content Accuracy Measured quantities are assessed to ensure alignment between calculated concentration and documented specifications.
Quality & Safety Parameters Samples are evaluated to confirm acceptable limits for residual processing agents and the absence of microbial contamination.
Lot-Level Traceability Each unit is associated with identifiable batch records, supporting traceability and internal quality control continuity.
