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10.1016/j.xpro.2021.101067

http://scihub22266oqcxt.onion/10.1016/j.xpro.2021.101067
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suck abstract from ncbi


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pmid34901888      STAR+Protoc 2022 ; 3 (1): 101067
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  • Detection of N6-methyladenosine in SARS-CoV-2 RNA by methylated RNA immunoprecipitation sequencing #MMPMID34901888
  • Li N; Rana TM
  • STAR Protoc 2022[Mar]; 3 (1): 101067 PMID34901888show ga
  • N (6) -methylation of adenosine (m6A) is the most abundant internal mRNA modification and is an important post-transcriptional regulator of gene expression. Here, we describe a protocol for methylated RNA immunoprecipitation sequencing (MeRIP-Seq) to detect and quantify m6A modifications in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA. The protocol is optimized for low viral RNA levels and is readily adaptable for other applications. For complete details on the use and execution of this protocol, please refer to Li et al. (2021).
  • |Adenosine/*analogs & derivatives/analysis/genetics[MESH]
  • |Animals[MESH]
  • |COVID-19/genetics[MESH]
  • |Caco-2 Cells[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Gene Expression Regulation/genetics[MESH]
  • |Gene Expression/genetics[MESH]
  • |Genetic Techniques[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Immunoprecipitation/*methods[MESH]
  • |Methylation[MESH]
  • |RNA Processing, Post-Transcriptional[MESH]
  • |RNA, Viral/metabolism[MESH]
  • |RNA/chemistry/genetics[MESH]
  • |SARS-CoV-2/genetics/pathogenicity[MESH]
  • |Sequence Analysis, RNA/*methods[MESH]


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