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potential to become an important component in structural studies of bio-macromolecules. The main reason for its attractiveness lies in the possibility of using these data to quickly distinguish between
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are neutrons spectroscopy and scattering which allows us to measure the time scales and length scales of interest with the unique ability to selectively probe a portion of the assembly by isotopic labelling. key
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identification of its chemical components. The most sensitive and widely employed method for making such identifications involves matching tandem spectra acquired via liquid chromatography tandem mass spectrometry
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