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Status |
Public on Jul 01, 2021 |
Title |
High-resolution transciptome mapping and N6-methyladenosine modification mapping of RAW264.7 cell lines treated with TCP, TBP or TIP. |
Organism |
Mus musculus |
Experiment type |
Methylation profiling by high throughput sequencing
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Summary |
Purpose:Detect transcriptome-wide mapping of m6A modifications by MeRIP-seq between normal and chemical-treated RAW264.7 cells. Methods:Total RNA was extracted using TRIzol Reagent followed by chemical fragmentation. The fragmented RNA was incubated with anti-m6A antibody. The desired m6A-enriched RNA eluate was used to construct cDNA library in parallel with input control. Conclusion: Our study revealed the difference of m6A-methylated RNA between normal and TCP/TBP/TIP-treated cells by RNA-seq and MeRIP-seq technologies.
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Overall design |
Compare the difference of m6A-methyalated RNA between normal and TBP/TCP/TIP treated samples.
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Contributor(s) |
Huang L, Zhang J |
Citation missing |
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Submission date |
May 19, 2021 |
Last update date |
Jul 02, 2021 |
Contact name |
Zhang Jun |
E-mail(s) |
3219030654@stu.cpu.edu.cn
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Phone |
15651718659
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Organization name |
China Pharmaceutical University
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Lab |
zhoulab
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Street address |
longmiandadao
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City |
nanjing |
State/province |
jiangsu |
ZIP/Postal code |
211198 |
Country |
China |
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Platforms (1) |
GPL24247 |
Illumina NovaSeq 6000 (Mus musculus) |
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Samples (8)
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Relations |
BioProject |
PRJNA731051 |
SRA |
SRP320476 |