2014
DOI: 10.1016/j.jphotobiol.2014.06.004
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Identification of protein phosphatase interacting proteins from normal and UVA-irradiated HaCaT cell lysates by surface plasmon resonance based binding technique using biotin–microcystin-LR as phosphatase capturing molecule

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Cited by 4 publications
(2 citation statements)
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“…Previous reports revealed that PP2Ac interacts with the regulatory subunit (MYPT1) of myosin phosphatase in cells, which regulates motility of invasive stages of the parasite (Becsi et al. ; Green et al. ).…”
Section: Discussionmentioning
confidence: 99%
“…Previous reports revealed that PP2Ac interacts with the regulatory subunit (MYPT1) of myosin phosphatase in cells, which regulates motility of invasive stages of the parasite (Becsi et al. ; Green et al. ).…”
Section: Discussionmentioning
confidence: 99%
“…Effectiveness of the experiment, however, always depends on the optimal binding, washing and elution conditions, and resulting specificity and compatibility for the PPIs of interest. PPIs can be also quantified using surface plasmon resonance (SPR) (12,13), which has been used almost exclusively in validation experiments with purified proteins up-to-date (14)(15)(16)(17)(18), with a single exception (19).…”
mentioning
confidence: 99%