Direct partition through ultrafiltration was applied to develop a method for the study of nucleotide binding to ribonucleotide reductase from Escherichia coli. The assay involved a 0.5- to 1-min centrifugation step where bound and unbound nucleotides are separated over an ultrafiltration membrane. N
A nitrocellulose filter binding assay for ribonucleotide reductase
✍ Scribed by Karin Söderman; Peter Reichard
- Book ID
- 107714284
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 404 KB
- Volume
- 152
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The ability to bind to nitrocellulose is commonly accepted as being a universal property of proteins and has been widely used in many different fields of study. This property was first exploited in the study of DNAbinding proteins 30 years ago, in studies involving DNA binding by the lactose repress
A sensitive, rapid, and accurate assay for measuring ribonucleotide reductase activity, including the reduction of CDP. UDP, GDP. and ADP to their corresponding deoxyribonucleotides, is described. Using polyethyleneiminecellulose thin-layer chromatography, I was able to separate the substrates, the