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For Research Teams
An academic lab cites a standard for years; a discovery team needs a locked route from pilot to scale-up; a CRO needs documentation that reconciles across sites; a core facility needs one stable catalogue identity its whole department can reference. Each page below covers how that buyer qualifies, documents, and re-orders Lyochem reference standards.
Universities, medical schools, and government institutes qualifying a reference standard for a method-development or in-vivo workflow.
Global · concentrated in USA · EU · UK · Japan · Australia
How they source
Biotech R&DPreclinical biotech and pharma discovery teams sourcing characterized peptides for receptor-pharmacology, screening, and method-development campaigns.
USA · EU · UK · Switzerland · Singapore · APAC discovery hubs
How they source
CROsCROs running preclinical and translational studies for sponsors who need traceable reference material reconciled across multi-site campaigns.
Global · USA · EU · India · China · APAC CRO clusters
How they source
Core facilitiesShared instrumentation cores and mass-spec facilities holding reference standards for cross-PI method validation and reagent qualification.
Global · concentrated at university medical centres + national labs
How they source
First reply under 12 hours from a synthesis chemist or analytical contact — not a templated auto-response. Lot-specific HPLC chromatogram, ESI-MS identity, MS/MS sequence (on request), KF water, and stability data returned with the quote.