Custom peptide synthesis: difference between revisions
Diff·revision 9 → 10·14:46, 15 Feb 2025
Difference between revision 9 and revision 10 of Custom peptide synthesis. 6 lines changed; the page grew by 150 bytes.
| Revision 9 — 07:51, 25 Jan 2025 FmocFrancis (talk) state the residual-moisture target with the method it is measured by 3,249 bytes +35 | Revision 10 — 14:46, 15 Feb 2025 CouplingCillian (talk) add the crimp-seal step to the fill-and-finish description 3,399 bytes +150 | ||
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| 37 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref> | 37 | <ref name="usp1503">United States Pharmacopeia, General Chapter <1503>, ''Quality Attributes of Synthetic Peptide Drug Substances''.</ref> |
| 38 | 38 | ||
| + | 39 | == See also == | |
| + | 40 | * [[Peptide synthesis]] | |
| + | 41 | * [[Contract development and manufacturing organisation]] | |
| + | 42 | * [[Certificate of analysis]] | |
| + | 43 | * [[Peptide content]] | |
| + | 44 | ||
| 39 | {{DEFAULTSORT:Custom peptide synthesis}} | 45 | {{DEFAULTSORT:Custom peptide synthesis}} |
| 40 | [[Category:Peptide synthesis]] | 46 | [[Category:Peptide synthesis]] |