A Clean, More Efficient Method for In-Solution Digestion of Protein Mixtures without Detergent or Urea
Proteolytic digestion of a complicated protein mixture from an organelle or whole-cell lysate is usually carried out in a dilute solution of a denaturing buffer, such as 1−2 M urea. Urea must be subsequently removed by C18 beads before downstream analysis such as HPLC/MS/MS or complete methylation f...
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Veröffentlicht in: | Journal of proteome research 2006-12, Vol.5 (12), p.3446-3452 |
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