Zhang Lab's CRISPR Frequently Asked Questions
Type
Collection
...the second design (in pX330 / PX335 ), so we recommend people all use the pX330/PX335 system ....the oligo when cloning my target spacers into the PX330 vector backbone? There is no need to add the NGG...having a targeting spacer cloned into the backbone ( pX330 or PX335 , depending if you want to use wildtype...wildtype Cas9, clone two spacers for each locus into PX330, then co-transfect or delivery the two plasmids ...not a very big concern, you could go ahead with PX330 plasmid, clone in your target guides, test run them...into the cells with the Cas9/sgRNAs vector (like PX330). For large changes (>100bp insertions or deletions...if the cloning of my oligo into a backbone like PX330 worked? You can quickly check which of your colonies...