Research Capabilities
Our Services
High-purity peptide synthesis, analytical validation, and custom modifications for pharmaceutical and academic research.
SYN-SPPS-01
Turnaround: 5 – 10 days
Core Capability
Solid-Phase Peptide Synthesis
High-efficiency SPPS for rapid, scalable peptide production.
Key Features
- Standard Fmoc/tBu chemistry for high-purity yields
- Scalable synthesis from milligram to multi-gram batches
- Optimized coupling cycles for difficult sequences
- Rigorous monitoring of coupling efficiency per cycle
PUR-HPLC-02
Turnaround: 3 – 5 days
Core Capability
Advanced HPLC Purification
Precision HPLC purification for research-grade peptide purity.
Key Features
- Preparative HPLC for high-resolution separation
- Custom gradient optimization for complex mixtures
- TFA removal and counter-ion exchange services
- Lyophilization for stable, powder-form delivery
ANA-VAL-03
Turnaround: 24 – 48 hours
Core Capability
Analytical Validation Suite
Comprehensive analytical data for every synthesized batch.
Key Features
- ESI-MS and MALDI-TOF mass verification
- Analytical HPLC purity profile documentation
- Amino acid analysis for precise quantification
- Solubility and stability testing protocols
LAB-DYE-04
Turnaround: 7 – 14 days
Core Capability
Custom Dye & Isotope Labeling
Site-specific labeling for advanced imaging and tracking.
Key Features
- N-terminal and C-terminal fluorescent tagging
- Stable isotope labeling (13C, 15N) for NMR studies
- Biotin and PEGylation for enhanced solubility
- Site-specific conjugation to carrier proteins
ENG-CMP-05
Turnaround: 10 – 21 days
Core Capability
Complex Peptide Engineering
Specialized synthesis for cyclic and stapled peptide structures.
Key Features
- Head-to-tail and side-chain cyclization
- Hydrocarbon stapling for conformational stability
- D-amino acid and non-natural amino acid incorporation
- Multi-disulfide bridge formation expertise
Purity Standards
Peptide Quality Tiers
Select the validation grade that matches your research requirements. From screening to clinical trials.
Early-stage R&D
Crude Grade
Rapid synthesis for initial screening
InvestmentEntry-level pricing
Specifications
- Crude purity assessment
- Standard MS validation
- Rapid 3-day synthesis
- Basic sequence report
- Lyophilized delivery
Recommended
Immunology research
Immuno Grade
Optimized for antibody production
InvestmentMid-tier investment
Specifications
- ≥85% purity validation
- RP-HPLC analysis included
- MALDI-TOF verification
- Detailed QC certificate
- Optimized for conjugation
- Batch consistency tracking
Pre-clinical trials
Clinical Grade
cGMP-compliant research standards
InvestmentPremium validation
Specifications
- ≥98% purity validation
- Full analytical suite (AAA/MS)
- TFA removal & salt control
- Endotoxin testing included
- Stability study reports
- Full traceability audit
Analytical Matrix
Validation Comparison
Analytical techniques by grade
| Metric | Crude | Immuno | Clinical |
|---|---|---|---|
| Analytical Validation | |||
Purity Threshold | Crude | ≥85% | ≥98% |
Mass Verification | Standard MS | MALDI-TOF | High-Res MS/MS |
Amino Acid Analysis | Not included | Upon request | Standard inclusion |
| Quality Control Protocols | |||
QC Reporting | Basic summary | Standard COA | Full documentation |
Endotoxin Testing | Not included | Optional | Included |
Salt/Counter-ion | Standard | Controlled | TFA-free/Custom |
| Service & Compliance | |||
Turnaround Time | 3-5 days | 7-10 days | 14+ days |
Regulatory Support | null | Standard | Full cGMP-ready |
Technical Support | Email support | Dedicated lead | Scientific liaison |
Need custom validation for your specific research?
Contact Our LabSynthesis Inquiry
Submit Your Peptide Specifications
Provide your sequence, purity requirements, and quantity targets. Our team will conduct a rapid feasibility assessment to ensure your research goals are met with precision.
No-cost feasibility
Expert validation
Strict compliance
48h Response
Rapid Feasibility Review
Direct consultation with lead chemists to evaluate your sequence complexity and synthesis requirements.
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Secure Data Protocol
Enterprise-grade confidentiality for all proprietary peptide sequences and research specifications.
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Custom Synthesis Plan
Receive a detailed technical proposal including purity targets and analytical validation methods.
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