A method is described for the rapid purification of acid deoxyribonucleases. It primarily involves chromatography of the enzyme-containing preparation through a DNA-ECTEOLA-cellulose column. This column retains the DNAse activity but not the inactive protein, and consequently, high degrees of purifi
A rapid method for fractionation and purification of a 92 kDa cartilage glycoprotein
✍ Scribed by Andreas E. Roussidis; Stavros T. Anagnostides
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 96 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0269-3879
- DOI
- 10.1002/bmc.294
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