![]() Furthermore, the reproducibility in relative quantification of the proteins is even higher in samples precipitated with acetone compared with the original sample.Īcetone Protein precipitation SWATH TCA/acetone Technology. From this study, it was possible to conclude that in the case of diluted samples in denaturing buffers, the use of cold acetone as precipitation protocol is more favourable than the use of TCA/acetone in terms of reproducibility in protein recovery and number of identified and quantified proteins. The amount of protein recovered after acetone and TCA/acetone precipitation was assessed, as well as the protein identification and relative quantification by SWATH-MS yields were compared with the results from the same sample without precipitation. It is one of the first of the series of lyotropic salts and. In this work, two protein precipitation approaches, widely used for cleaning and concentrating protein samples, were tested and compared in very diluted samples solubilized in a strong buffer (containing SDS). The most common salt for protein precipitation is ammonium sulfate, as described by Burgess (2009). We have often found that 100 mM l-arginine is useful for stabilizing protein samples against slow precipitation. Nonetheless, sample preparation prior to mass spectrometry analysis is of the utmost importance. ![]() Proteomic approaches are extremely valuable in many fields of research, where mass spectrometry methods have gained an increasing interest, especially because of the ability to perform quantitative analysis. ![]()
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