Find the record
Documentation should be easy to locate.
Use the lot-document library and technical-support pathway to locate available records by catalog or lot reference.
Certificates of Analysis
Search by catalog number and lot, then review the release document and supporting data.
Storage & material notes
Product-specific handling, storage and transport information tied to the technical record.
RFQ preparation guide
Sequence, scale, modification, purity, analytics, presentation and required date.
Responsible-use FAQ
What does “research use only” mean?
It describes materials intended for legitimate non-clinical laboratory investigation. It does not authorize administration to humans or animals, compounding, diagnosis, treatment or consumer use.
Are catalog records available for purchase?
Stocked research products display current pack options, availability and pricing on their product records. Bulk API and custom-synthesis requests use a qualification and written-quotation pathway.
How is bulk API supplied?
Bulk research API records describe Remetide-manufactured material beginning in 100 g increments. They are quotation-only: organization, intended use, specification, analytical package, packaging, destination, feasibility, lead time and applicable legal or intellectual-property review must be completed before an order can be accepted.
Can I submit a peptide sequence for design or synthesis?
The workflow accepts a sequence or target concept, intended assay context, scale, target purity, modifications, format, analytics and timeline for technical review. Acceptance, feasibility, price and deliverables require a written project scope.
Can I request a peptide library or conjugate?
The project pathway includes libraries, labels, linkers, cyclization and conjugation concepts. The actual chemistry, library size, QC plan, yield and format must be confirmed before a project is accepted.
Does the catalog include small-molecule work?
Yes. The small-molecule pathway accepts a structure, SMILES string, target concept or literature reference for route, safety, scale, purification and analytical review. Capability and deliverables are confirmed through technical review.
What documents accompany a research material?
The documentation package may include a lot-specific COA, analytical summary, material specification and handling statement. Actual documents depend on the approved specification and project agreement.
How is purity described?
Purity identifies the analytical method and defers to the released lot result and molecule-specific specification.
Does Simple Life Science provide dosing or administration guidance?
No. We do not provide dosing, administration, medical advice or patient-specific guidance.
How are custom projects evaluated?
A technical review considers sequence, structure or item, intended laboratory context, scale, modifications, specification, analytics, presentation, timeline, safety, documentation and third-party rights.