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Empirical Evidence of Cellular Histidine Phosphorylation by Immunoblotting Using pHis mAbs.

Methods in molecular biology (Clifton, N.J.) (2019-11-11)
Rajasree Kalagiri, Kevin Adam, Tony Hunter
RÉSUMÉ

Immunoblotting is a ubiquitous immunological technique that aids in detecting and quantifying proteins (including those of lower abundance) and their posttranslational modifications such as phosphorylation, acetylation, ubiquitylation, and sumoylation. The technique involves electrophoretically separating proteins on an SDS-PAGE gel, transferring them onto a PVDF (or nitrocellulose) membrane and probing with specific antibodies. Here we describe an immunoblotting technique for detecting cellular phosphohistidine, a labile posttranslational modification, by optimizing experimental conditions such that the labile phosphohistidine signal is conserved throughout the experiment.

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Sigma-Aldrich
Anticorps anti-N1-phosphohistidine (1-pHis), clone SC1-1, clone SC1-1, from rabbit
Sigma-Aldrich
Anticorps anti-N3-phosphohistidine (3-pHis), clone SC56-2, clone SC56-2, from rabbit
Sigma-Aldrich
Anti-N1-Phosphohistidine (1-pHis) Antibody, clone SC50-3, clone SC50-3, from rabbit