Our testing capabilities
A four-stage analytical workflow applied to every lot, before it ever reaches a customer.
HPLC Purity Analysis
Every batch is run through high-performance liquid chromatography to confirm peptide purity of ≥99%, with chromatograms retained for each lot.
Mass Spectrometry
MALDI-TOF and ESI-MS verify the exact molecular weight and sequence integrity of each peptide against its reference standard.
Endotoxin & Sterility
LAL endotoxin testing and USP sterility assays confirm each vial is safe for reconstitution and laboratory research use.
Content Accuracy
UV spectrophotometry and amino-acid analysis quantify net peptide content, so every reconstitution calculation is exact.
Inside our laboratory
A closer look at the facilities, equipment and processes behind every verified peptide we ship.
From synthesis to your door
A documented chain of custody that guarantees the integrity of every vial.
Raw Material Sourcing
Pharmaceutical-grade lyophilised peptides sourced from GMP-certified synthesis partners.
In-House HPLC Testing
Each lot is analysed for purity and impurities before it enters our cold store.
Mass & Sequence Verification
Molecular weight and amino-acid sequence confirmed by mass spectrometry.
Cold-Chain Storage
Verified vials are held at −20°C in monitored freezers until dispatch.
Certificate of Analysis
A lot-specific CoA is generated and retained for every batch we ship.
Monitored cold-chain storage
Verified vials are stored at −20°C in continuously monitored laboratory freezers with backup power. Orders are dispatched in insulated, cold-pack packaging so peptides arrive stable and potent anywhere in Australia.
Certificate of Analysis
Every batch ships with a lot-specific Certificate of Analysis documenting HPLC purity, mass-spec confirmation and net content. Researchers can request any lot's CoA before purchase — full transparency, no exceptions.
