Please use this identifier to cite or link to this item:
https://doi.org/10.21769/bioprotoc.2095
DC Field | Value | |
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dc.title | Dot Blot Analysis of N6-methyladenosine RNA Modification Levels | |
dc.contributor.author | Shen, Lisha | |
dc.contributor.author | LIANG ZHE | |
dc.contributor.author | YU HAO | |
dc.date.accessioned | 2020-06-02T00:56:58Z | |
dc.date.available | 2020-06-02T00:56:58Z | |
dc.date.issued | 2017-01-05 | |
dc.identifier.citation | Shen, Lisha, LIANG ZHE, YU HAO (2017-01-05). Dot Blot Analysis of N6-methyladenosine RNA Modification Levels. BIO-PROTOCOL 7 (1). ScholarBank@NUS Repository. https://doi.org/10.21769/bioprotoc.2095 | |
dc.identifier.issn | 2331-8325 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/168911 | |
dc.description.abstract | N6-methyladenosine (m6A) is the most prevalent internal modification of eukaryotic messenger RNA (mRNA). The total amount of m6A can be detected by several methods, such as dot blot analysis using specific m6A antibodies and quantitative liquid chromatography-tandem mass spectrometry (LC-MS/MS) (Fu et al., 2014; Shen et al., 2016). Here we describe the method for fast detection of total m6A levels in mRNA by dot blot analysis using a specific m6A antibody. | |
dc.publisher | Bio-Protocol, LLC | |
dc.source | Elements | |
dc.subject | Dot blot | |
dc.subject | RNA modification | |
dc.subject | m6A | |
dc.type | Article | |
dc.date.updated | 2020-06-01T10:02:19Z | |
dc.contributor.department | DEPT OF BIOLOGICAL SCIENCES | |
dc.description.doi | 10.21769/bioprotoc.2095 | |
dc.description.sourcetitle | BIO-PROTOCOL | |
dc.description.volume | 7 | |
dc.description.issue | 1 | |
dc.published.state | Published | |
dc.grant.id | MOE2015-T2-1-002 | |
dc.grant.id | NRF-NRFI2016-02 | |
dc.grant.fundingagency | Ministry of Education-Singapore | |
dc.grant.fundingagency | Singapore National Research Foundation Investigatorship Programme | |
Appears in Collections: | Staff Publications Elements |
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Bio-protocol-2017.pdf | 272.46 kB | Adobe PDF | OPEN | Published | View/Download |
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