HPLC/UPLC purity assessment
Technical scope, quality level, batch documents and delivery requirements can be configured according to project stage.
Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.
Analytical characterization for identity, purity, batch consistency and development decision making.
Project Discussion
Share your target sequence, purity, scale, modification, delivery format and documentation requirements. Quantai will review feasibility and respond with a practical quotation route.
Core Capabilities
LC-MS and MALDI-TOF confirmation
Technical scope, quality level, batch documents and delivery requirements can be configured according to project stage.
Amino acid composition and impurity review
Technical scope, quality level, batch documents and delivery requirements can be configured according to project stage.
Batch documentation and method support
Technical scope, quality level, batch documents and delivery requirements can be configured according to project stage.
Typical Workflow
1Requirement review
2Technical feasibility
3Quotation and timeline
4Synthesis or process execution
5QC documentation
6Shipment and follow-up
| Development Stage | Our Peptide Support |
|---|---|
| Concept & Feasibility | Peptide design strategy, sequence optimization and feasibility assessment |
| Discovery Research | Custom peptide synthesis, targeting peptide design and functional screening support |
| Lead Optimization | Peptide modification, conjugation strategy and structure-function optimization |
| Process Development | Route optimization, process robustness and impurity control strategy |
| GMP Manufacturing | GMP-compliant peptide synthesis, quality documentation and batch release support |