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Custom peptide synthesis: difference between revisions

Diff·revision 10 → 11·06:41, 14 Mar 2025

Difference between revision 10 and revision 11 of Custom peptide synthesis. 3 lines changed; the page grew by 378 bytes.

Revision 10 — 14:46, 15 Feb 2025
CouplingCillian (talk)
add the crimp-seal step to the fill-and-finish description
3,399 bytes +150
Revision 11 — 06:41, 14 Mar 2025
DiluentDiya (talk)
close an unbalanced quotation mark
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32Declining to quote is also informative and is not a negative signal. Some sequences are genuinely difficult, some require capability a given house does not have, and a house that declines rather than accepting and failing is behaving reasonably.32Declining to quote is also informative and is not a negative signal. Some sequences are genuinely difficult, some require capability a given house does not have, and a house that declines rather than accepting and failing is behaving reasonably.
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+34Quotations for sequences corresponding to compounds under patent, or to controlled substances, raise separate questions that are legal rather than technical. This wiki does not advise on them; see [[Regulatory status by jurisdiction]] and [[Patent expiry and biosimilars]].{{r|iso9001}}
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34== References ==36== References ==
35{{reflist}}37{{reflist}}
36<ref name="behrendt2016">Behrendt R, White P, Offer J. "Advances in Fmoc solid-phase peptide synthesis." ''Journal of Peptide Science'' 22(1):4–27 (2016). PMID 26785684.</ref>38<ref name="behrendt2016">Behrendt R, White P, Offer J. "Advances in Fmoc solid-phase peptide synthesis." ''Journal of Peptide Science'' 22(1):4–27 (2016). PMID 26785684.</ref>
37<ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref>39<ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref>
+40<ref name="iso9001">ISO 9001:2015, ''Quality management systems — Requirements''.</ref>
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39== See also ==42== See also ==