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Research Use Only, not for human or veterinary consumption Ships across the EU single market Verified, every batch
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Resources, knowledge, calculators

A reference shelf
for working researchers.

Calculators for peptide reconstitution, dilution maths, and molarity conversion. A nomenclature guide for amino acid one and three letter codes. A pharmacological glossary covering the terms used across our editorial and product pages. Methodology references on how third-party verification is performed. Free to use, no signup, no gate.

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resources, calculators, and reference tools
All tools render in-browser. None require signup. None capture data. Engineered for the bench, not for analytics.
02, references

Reference texts.

Glossaries, nomenclature guides, and pharmacological references. Open in a tab, search the page, get the term, return to your work.

Guide 05

Peptide nomenclature
guide.

Amino acid one-letter and three-letter codes. Standard naming for peptide bonds, terminal modifications, salt forms, and post-translational modifications. The reference researchers reach for when reading sequences.

Open guide →
Guide 06

Pharmacological
glossary.

Definitions for thirty terms used across our editorial and product pages: HPLC, LC-MS, CLND, FTIR, endotoxin LAL, bioburden, lyophilization, IC50, K-d, agonist, antagonist, secretagogue, allosteric modulator, and others.

Open glossary →
Guide 07

Methodology
reference.

How Cresten verifies every batch. Janoshik Analytical’s methodology, Ph. Eur. specification references, the four-panel current testing scope, and the seven-panel target. Salt-form policy. Storage stability protocols.

Open methodology →
Guide 08

Reading a peptide
chromatogram.

A working researcher’s walkthrough of a typical HPLC chromatogram on a peptide COA. What the main peak, retention time, baseline drift, and minor peaks tell you. What is normal, what is a flag.

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Guide 09

Janoshik vs in-house
QA.

Why Cresten uses Janoshik Analytical for every batch instead of internal QA. The difference between in-house testing on supplier-provided samples and third-party verification on our own received stock.

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Guide 10

EMA guidance,
April 2026.

A reading of the European Medicines Agency’s most recent peptide guidance updates and what they signal for the EU research peptide market. Operating-phase reference, not legal advice.

Read editorial →