I am naive to this CRISPR/Cas9 system for gene editing. As a part of my research project, I want to establish this protocol in my lab to knockout the E6 and E7 oncogene of HPV16 and HPV18 virus. I have designed the gRNA using the ZiFit software and now I have to clone the gRNA fragments. Can anyone suggest me a good and easy protocol for cloning gRNA fragments? Also the software has suggested nearly 7 gRNA, do I have to clone them all and screen one by one to check the efficiency of gene knockout?