We extracted total RNA samples for high-through RNA sequencing from CAL-62 cells transfected with LINC00886 smart silencer and negative control. Then RNA-seq analyses were generated by deep sequencing
HEK293T ishXrn1 cells were treated with doxycycline for 3-4 days to induce knock down of Xrn1, then transfected with a luciferase reporter with or without a 99bp sequence from the STOML2 gene inserted
