sgRNA Target Selection and Homology-directed Repair Template Design
2:21
Prepare Injection Mix and Injection Protocol
3:18
Screen P0 Plates and Single mCherry(+) F1s
4:03
Single Worm PCR and Genotyping
5:41
Indentification and Sequence Verification of Edited Animals
6:34
Results: Rapid CRISPR/Cas9 Generated Point Mutations in C. elegans sod-1
7:50
Conclusion
Transcript
The overall goal of this procedure is to generate genomic point mutations in C.Elegans using single stranded oligonucleotide homology directed repair templates and CRISPR/Cas9 ribonucleoproteins. This method can help answer key questions in the ne
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여기, 우리는 CRISPR-Cas9 ribonucleoproteins 및 homology 종속 복구 서식 파일을 사용 하 여 C. 선 충 의 게놈을 엔지니어링 하는 방법 제시.