Untargeted mass spectrometry analysis of complex samples such as entire prokaryotic or eukaryotic cell lysates that are directly spotted in the MALDI ionisation/desorption matrix offers a fast method for rapid identification of bacteria [ 22] but also the discrimination/authentication of mammalian and insect cell lines [ 23- 26].
Major spots were very efficiently analyzed by the TLC HPLC MS system, leading to the rapid identification of several bioactive alkaloids (Table 2), including berberine, chelerithrine, coptisine, protopine, sanguinarine, galanthamine, magnoflorine, and palmatine.
Here, we demonstrate a high-throughput methodology allowing rapid identification of the proteins binding to a given human RNA molecule using a protein microarray containing ~9,400 human recombinant proteins spotted in duplicate.
This would allow rapid identification of Cas9 mutants that function more effectively with crXNA in vivo.
Junutula, J. R. et al. Rapid identification of reactive cysteine residues for site-specific labeling of antibody-Fabs.
Telenti, A. et al. Rapid identification of mycobacteria to the species level by polymerase chain reaction and restriction enzyme analysis.
Safarova, M. S., Liu, H. & Kullo, I. J. Rapid identification of familial hypercholesterolemia from electronic health records: The SEARCH study.
Our high-throughput pgRNA genome deletion method will enable rapid identification of functional mammalian non-coding elements.
Species-specific primers designed allowed rapid identification of these species.
Plant biosecurity requires rapid identification of pathogenic organisms.
More research and development is required for kits that will allow rapid identification of pathogens, and we need more and faster work on vaccines and antidotes.
