Difference between revisions of "Part:BBa K3791004:Design"
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===References=== | ===References=== | ||
+ | [1] New England Biolabs. (s/f). <b>How do I design a guide RNA for use with EnGen Lba Cas12a?</b> Neb.com. From: https://international.neb.com/faqs/2018/05/03/how-do-i-design-a-guide-rna-for-use-with-engen-lba-cas12a |
Revision as of 00:32, 10 October 2021
Spacer gRNA Spectinomycin
- 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
For choosing which fragment of the spectinomycin-resistant gene we used for our spacer design, we had to take into account the PAM sequence needed by the nature of LbCas12a. In our case, the PAM sequence was TTTV, where V is any nucleotide except T. The PAM must be placed in the 5' extreme of the complementary chain of the one being targeted and must not appear in the target sequence. [1]
Another important consideration to bear in mind was that the spacer length was required to be between 18 and 24 nucleotides. [1]
Source
This part is the complementary sequence of an spectinomycin-resistant gene DNA fragment.
References
[1] New England Biolabs. (s/f). How do I design a guide RNA for use with EnGen Lba Cas12a? Neb.com. From: https://international.neb.com/faqs/2018/05/03/how-do-i-design-a-guide-rna-for-use-with-engen-lba-cas12a