Public COA audit
Limulus Amebocyte Lysate (LAL) · SS-31
Audited July 28, 2026
Several fields check out, but we found issues worth reviewing before you rely on this document.
- Legitimacy
- 92
- Confidence
- 88%
- Panels
- 1/7
Document details
Fields extracted from the certificate — not order or payment data.
- Batch / lot
- 26-3-45959
- Sample date
- 2025-11-19
- Issue date
- 2025-11-19
7-panel checklist
Had data + good, had data + bad, reported without pass/fail, or missing. Missing lowers thoroughness — you decide whether that panel matters; PeptIQ’s score still factors coverage.
1 of 7 present · 1 passed · 0 failed · 0 reported · 6 missing
Missing is a thoroughness gap — not automatically bad. PeptIQ’s legitimacy score still weighs panel coverage; you can down-weight panels that don’t matter for your use case.
Identity
Not on this COA · core
Compound identity confirmed (e.g. HPLC, mass spec).
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Purity
Not on this COA · core
Reported purity percentage for the analyte.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Heavy metals
Not on this COA
Lead, arsenic, cadmium, mercury, or similar limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Microbial
Not on this COA
Bioburden / microbial limits testing.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Endotoxin
Tested · passed · core
LAL or chromogenic endotoxin assay.
< 0.050 EU/mL
Sterility
Not on this COA
Sterility testing where applicable.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
Residual solvent / water
Not on this COA
Residual solvents or water content limits.
No evidence for this panel. That lowers thoroughness — whether it matters depends on what you care about.
How to read this
Had data · good
Panel present with a pass (or clear acceptance).
Had data · bad
Panel present with a fail — a concrete quality signal.
Had data · unclear
Value reported without an explicit pass/fail mark.
Missing
Not on this certificate. Lowers thoroughness; you decide if that panel matters for your use case. PeptIQ’s score still factors coverage.
Findings
Evidence-linked observations from this audit.
Endotoxin testing performed
Endotoxin level measured at < 0.050 EU/mL, well below the acceptable threshold of 0.25 EU/mL. Sample passes endotoxin limit test using validated chromogenic LAL assay.
Batch information present
Sample lot number 26-3-45959 clearly documented with sample concentration (10 mg) and vials received (1).
Test date documented
Test date 11/19/2025 and analyst signature date 11/19/2025 are consistent and within acceptable range.
Testing lab identified
BioRegen identified as testing lab with contact information ([email protected], www.bioregen.com) and verification instructions provided.
Limited testing scope
This report only covers endotoxin testing. No identity confirmation, purity analysis, heavy metals, microbial contamination, sterility, or residual solvent testing is included. This is a specialized endotoxin-only report, not a comprehensive COA.
Professional presentation
Report includes proper header with Report ID (BL-ENDO-251911-184), validation key (BIOLABS2010), QR code for verification, analyst signature, and detailed reagent information including cartridge lot, calibration code, and spike recovery data.
PeptIQ COA reports analyze document content and publicly verifiable lab signals. They are educational and not a guarantee of product quality, legality, or safety. Always consult a qualified professional before making health decisions. We never publish purchase prices, shipping details, or uploader identity.