Show your work.
The COA registry indexes the analytical reports for every active lot we distribute — third-party HPLC purity, LC-MS identity, and lot-level traceability.
Analytical scope
What the COA covers
Method
What it verifies
Read-out
HPLC / UPLC
Purity, related-substance profile
% target peptide vs. impurities
LC-MS
Identity, molecular weight
Observed m/z vs. theoretical
Mass / content
Quantitative dose per vial
mg recovered, batch-averaged where noted
Sterility screen
Microbiological burden (select lots)
Pass / fail per laboratory scope
How to read it
Five fields to check on every report.
- 01Lot number. Should match the printed lot on the vial label.
- 02Issuing laboratory. Named third party; not Lumineris.
- 03Report date. Tied to the lot, not the product line.
- 04Purity result. Typically ≥99% by HPLC; method noted.
- 05Identity result. Observed mass vs. theoretical mass for the target peptide.
Browse the registry
The full library is mirrored to a public spreadsheet, updated as new lots are tested.
Lumineris materials are Research Use Only (RUO). The COA registry compiles analytical results from internal, contracted, and independent laboratories; data is provided for documentation only and should be independently reviewed before experimental application. Not for human or animal consumption.