COA Overview
This page summarizes SynerGen’s quality workflow and laboratory testing panels. Item-level COAs aren’t linked from product cards; instead, use this reference and contact us for batch-specific reports if needed.
QA Policy: Each batch must meet ≥ 98.7% (HPLC). If any finished batch returns < 98.7%, the batch is destroyed and re-manufactured prior to release.
Release threshold: 98.7%
Identity
MALDI-TOF / ESI-MS; amino acid composition; sequence confirmation as applicable.
Purity (HPLC)
Reversed-phase HPLC @ 214 nm. Passing: ≥ 98.7% area.
Water & Residue
Karl Fischer moisture; residue on ignition for inorganic content.
pH & Appearance
1% w/v solution pH window; visual inspection white to off-white powder.
Bioburden
TAMC/TYMC screening per compendial guidance for research materials.
Endotoxin
LAL (gel-clot/kinetic, as applicable) for process hygiene benchmarking.
In Stock → typical HPLC results reported as “≥ 98.7%”.
In Production → “Pending production” until QC release.
Batch Status Snapshot (from catalog)
Quick view of current catalog items and whether COA is pending or released.
| SKU | Name | Strength | Stock | QA |
|---|---|---|---|---|
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