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Questions related from Lelamekala Vengidasan
I produce CRISPR gRNA by using PCR method. I obtained 10ug of RNA from in-vitro transcription. But when I proceed to gel electroporesis analysis I can see any visible band. There was almost blank....
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I'm going to do point mutation correction by using CRISPR Ribonucleoprotein method and ss-ODN. Guide-RNA design softwares from the internet gave me few possible guideRNAs. I'm planning to use two...
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Vector : pet26(+) 5360bp Insert : 1500bp RE : NdeI and XhoI After digestion, I elute out single band from both vector and insert and continue with ligation using Quick Ligation form NEB....
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