Endotoxin testing
LAL endotoxin testing for research peptides
LAL-based bacterial endotoxin detection. Separate sample required to prevent cross-contamination. Quantitative EU/mL result with pass/fail certification and QR-verified certificate.
What we report
- ✓LAL kinetic turbidimetric assay
- ✓Sensitivity: 0.005 EU/mL
- ✓Quantitative EU/mL result
- ✓Pass/fail certification against your specification
- ✓QR-verified certificate
- ✓48–72h typical turnaround
A peptide can test at high purity and still contain bacterial endotoxin. LAL testing is the standard approach to detect these heat-stable contaminants in research materials. Results are reported for documentation and batch review — not as a clinical safety assessment.