Endotoxin testing
LAL endotoxin testing for research samples
LAL-based bacterial endotoxin detection for research materials. A separate sample is required to reduce cross-contamination risk. Results are reported as quantitative EU/mL with comparison to an agreed specification where provided.
Research use only. Not for human or veterinary use, clinical application, or administration.
What we report
- ✓LAL kinetic turbidimetric assay (where selected for scope)
- ✓Method sensitivity stated on the certificate for the run performed
- ✓Quantitative EU/mL result
- ✓Outcome vs client specification where an agreed limit is supplied
- ✓QR-linked registry certificate
- ✓Estimated turnaround communicated at order acceptance (typically several working days)
LAL testing detects bacterial endotoxin in research materials. Results are reported for documentation and batch review — not as a clinical safety assessment, release for human use, or regulatory approval.
Some endotoxin methods may be performed by qualified partner laboratories, including facilities in the European Union where required. See our laboratory partner disclosure.