Hi everyone,
I packed lentivirus from HEK293T cell line with lenticas9-blast #52962. I started selection with blasticidin 3 days post infection. Control group were dead and the infected cells were selected over one week. But it took at least one week to recover the cells (had to withdraw Blast) to have a decent number of cells to run WB ( is this normal?). However, when I did western blot to look at the expression using anti-FLAG (could detect both N- and C-terminus) and anti-Cas9 (ab191468, the one listed on the protocol). Only my positive control (protein of Cas9+ cells borrowed from neighbour lab) had the bands. I'm wondering why? For example, anything tricky for EFS promoter in leukemia cells or Blasticidin selection process? (I have sequenced/digested my prep of plasmid and am running transient transfection to check protein and all looks fine). Or is there any available Cas9 plasmid (better to be with colors, and does not have puro+ selection ) that could be used with the Gecko v2 crispr library (puro)? Thanks for any information ahead!!
Best,
Linlin