Difference between revisions of "Part:BBa K4830020:Design"
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<partinfo>BBa_K4830020 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4830020 SequenceAndFeatures</partinfo> | ||
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===Design Notes=== | ===Design Notes=== | ||
− | The design of TLR ngRNA 1 includes the U6 promoter, spacer | + | The design of TLR ngRNA 1 includes the U6 promoter, spacer and gRNA scaffold. |
===Source=== | ===Source=== | ||
− | The TLR ngRNA 1 design contains the spacer | + | The TLR ngRNA 1 design contains the spacer sequence, which was adapted from other ngRNAs in the Prime Editor 2 paper cited in References. With the help of TWIST Bioscience we synthesized those and other necessary sequences, and further combined with a 65777 backbone with a mCherry-stop-Clover insertion in our lab. |
===References=== | ===References=== |
Latest revision as of 15:33, 11 October 2023
TLR ngRNA 1
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
The design of TLR ngRNA 1 includes the U6 promoter, spacer and gRNA scaffold.
Source
The TLR ngRNA 1 design contains the spacer sequence, which was adapted from other ngRNAs in the Prime Editor 2 paper cited in References. With the help of TWIST Bioscience we synthesized those and other necessary sequences, and further combined with a 65777 backbone with a mCherry-stop-Clover insertion in our lab.
References
Anzalone AV, Randolph PB, Davis JR, Sousa AA, Koblan LW, Levy JM, et al. Search-and-replace genome editing without double-strand breaks or donor DNA. Nature. 2019 Oct 21;576.
Certo, M. T., Ryu, B. Y., Annis, J. E., Garibov, M., Jarjour, J., Rawlings, D. J., & Scharenberg, A. M. (2011). Tracking genome engineering outcome at individual DNA breakpoints. Nature Methods, 8(8), 671–676.