대규모 gRNA DNA 소스에서 라이브러리 제작에 대 한 범용 프로토콜

0:48

Digestion of DNA with MNase and Separation of DNA Fragments by PAGE

3:05

Isolation of DNA Fragments from PAGE Gels and Linker Generation

4:26

End Repair of Gel-purified Fragments and Linker Ligation

5:32

Size Selection and Assembly of Vector-insert Construct

6:18

Electroporation of TG1 Electrocompetent E. coli Cells

8:38

Results: a gRNA Library can be Generated from and Target DNA

9:56

Conclusion