Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1496
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dc.contributor.authorSengupta, Sagar-
dc.contributor.authorSaifi, Shabnam-
dc.contributor.authorMohammed, Aftab-
dc.contributor.authorHussain, Mansoor-
dc.date.accessioned2025-01-30T06:24:51Z-
dc.date.available2025-01-30T06:24:51Z-
dc.date.issued2022-12-
dc.identifier.urihttp://hdl.handle.net/123456789/1496-
dc.description.abstractMitochondrial polymerase gamma (PolγA) is the only replicative polymerase in mitochondria. To determine PolγA ubiquitylation in cells, Flag-PolγA and MITOL are overexpressed, and subsequently the immunoprecipitated Flag-PolγA is checked for ubiquitylation. Alternately, in vitro synthesized PolγA and MITOL are used to determine whether PolγA is ubiquitylated. Either anti-ubiquitin or anti-Flag antibody is used to detect the ubiquitylated product. Thus, we provide a detailed, reliable, highly reproducible protocol for detecting ubiquitylation of PolγA by MITOL, both in cells and in vitro. For complete details on the use and execution of this protocol, please refer to Hussain et al. (2021).en_US
dc.language.isoenen_US
dc.publisherThe Author(s). Published by Elsevier Inc. All rights reserved.en_US
dc.subjectCell biology; Genetics; Molecular biology; Protein biochemistry; Protein expression and purification.en_US
dc.titleProtocol to detect in vitro and in cell ubiquitylation of mitochondrial DNA polymerase gamma by mitochondrial E3 ligase MITOLen_US
dc.typeArticleen_US
dc.journalSTAR Protocen_US
dc.volumeno3en_US
dc.issueno(4)en_US
dc.pages101710.en_US
Appears in Collections:Signal Transduction-II, Publications

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