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GLOSSARY

LAL Assay

Also known as: Limulus amebocyte lysate assay; Bacterial endotoxins test; BET

Limulus amebocyte lysate assay — the standard method for detecting and quantifying bacterial endotoxin in a peptide preparation.

DEFINITION

The LAL assay (Limulus amebocyte lysate assay) is the pharmacopoeial standard for detecting and quantifying bacterial endotoxin. It exploits the fact that amebocytes from the horseshoe crab (Limulus polyphemus) contain a clotting-cascade enzyme system that is activated by picogram quantities of endotoxin.

LAL is performed in three principal formats: gel-clot (a semi-quantitative pass/fail at a defined sensitivity), turbidimetric and chromogenic (both quantitative). Results are reported in Endotoxin Units per millilitre (EU / mL) and converted to EU / mg based on the peptide concentration. Recombinant Factor C (rFC) assays offer an equivalent, animal- free alternative.

WHY IT MATTERS

LAL is the assay behind every endotoxin figure reported on a Certificate of Analysis for a research peptide.

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Published: 2026-08-12Updated: 2026-08-12