Thymosin alpha-1 was produced from its bacterial recombinant precursor via non-enzymatic acetylation, simplifying manufacturing by eliminating the need for enzymatic N-terminal acetylation.
Key findingThymosin alpha-1 was produced from its bacterial recombinant precursor via non-enzymatic acetylation, simplifying manufacturing by eliminating the nee
What the researchers found
Thymosin alpha-1 was produced from its bacterial recombinant precursor via non-enzymatic acetylation, simplifying manufacturing by eliminating the need for enzymatic N-terminal acetylation.
Why it matters
Relevant for peptide research.
How the study worked
research study.
What this study cannot tell us
See abstract.
How to read the evidence
emerging evidence.
When this study was published
Published in 2010.
The bigger picture
Advances peptide research.
Questions still open
- Further research needed.
Common questions
What was studied?
What was found?
Read the original research
Production of thymosin alpha1 via non-enzymatic acetylation of the recombinant precursor.
Biotechnology and applied biochemistry, 56(1), 17-25
Citation
Esipov, Roman S; Stepanenko, Vasily N; Beyrakhova, Ksenia A; Muravjeva, Tatjana I; Miroshnikov, Anatoly I. (2010). Production of thymosin alpha1 via non-enzymatic acetylation of the recombinant precursor.. Biotechnology and applied biochemistry, 56(1), 17-25. https://doi.org/10.1042/BA20100027