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资源简介：
The sequencing is to identify the DRIP peaks genome widely.
应用场景：
创建时间：
2022-05-01
相关数据集
RIP-seq analysis. Mus musculus strain:C57BL/6
To understand molecular mechanisms of RNA metabolisms mediated by PCBP1 in immune cells, RIP-seq analysis was carried out by using macrophages from mice.
NIAID Data Ecosystem60
Raw data of RIP-seq
Confluent HBMECs (4×107) organized in a monolayer were harvested for the sample preparation of RIP-sequencing. RNA-protein complexes were immunoprecipitated with antibodies targeted to occludin, then
NIAID Data Ecosystem50
Characterization of transcripts bound by LARP1 in the free 40S fraction isolated by sucrose gradients. Homo sapiens
RNA binding protein LARP1 binds preferentially to mRNAs containing a 5' Tract of Oligo Pyrimidines (5'-TOP) motif Overall design: RIP-seq performed with anti-LARP1 antibody or Normal Rabbit Serum cont
NIAID Data Ecosystem30
Non-canonical crRNAs derived from host transcripts enable multiplexable RNA detection by Cas9 [RIP-seq]
RIP-seq analysis to identify CjCas9 bound RNAs using co-immunoprecipitation and sequencing in CG84-21. Overall design: Cas9 was chromosomally tagged using 3xFLAG epitope at the C-terminus in Campyloba
NIAID Data Ecosystem50
Additional file 5 of RIP-seq reveals LINE-1 ORF1p association with p-body enriched mRNAs
Additional file 5: Table S1. L1EM estimates of locus specific LINE-1 expression for each of the samples.
Figshare2021-02-10 更新40
