RIP-seq analysis of LLC-PK1 cells transfected with the Flag-N/Flag-DDX5/Flag-RNMT plasmid and infected with PEDV (MOI = 1) was performed using an anti-Flag antibody.
To understand molecular mechanisms of RNA metabolisms mediated by PCBP1 in immune cells, RIP-seq analysis was carried out by using macrophages from mice.
We uncovered an unexpected function of mixed-lineage leukemia (MLL) protein, which is a critical epigenetic factor and whose disruption leads to leukemogenesis, in the functional regulation of miRNAs.
In this study we used RNA co-immunoprecipitation followed by RNA-sequencing (RIP-seq) to identify Hfq-binding RNAs in Vibrio cholerae. Overall design: V. cholerae wild-type and hfq::3XFLAG-tagged stra
Background: Immunotherapy, especially checkpoint inhibitors targeting PD-1 or PD-L1, has revolutionized cancer therapy. However, PD-1/ PD-L1 inhibitors have not been investigated thoroughly in gliobla
