Re-engineering the polymerase domain of Klenow fragment and evaluation of overproduction and purification strategies.
We describe experiments to produce large quantities of the polymerase domain of E. coli DNA polymerase I for biochemical and biophysical studies. The polymerase domain derivative used in previous studies was insoluble when overproduced and tended to aggregate during purification. These problems were...
محفوظ في:
| الحاوية / القاعدة: | Nucleic Acids Res |
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| المؤلفون الرئيسيون: | , , |
| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Oxford University Press
1993
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| الوصول للمادة أونلاين: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC310583/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8265361/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/21.23.5439 |
| الوسوم: |
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