Difference between revisions of "Part:BBa K2325003"
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<partinfo>BBa_K2325003 short</partinfo> | <partinfo>BBa_K2325003 short</partinfo> | ||
− | The BBa_K2325003 is a DNA sequence contains N20 | + | The BBa_K2325003 is a DNA sequence contains N20 associated with sgRNA. The N20 is selected from the genome of T7 phage, which is responsible for the synthesis of the DNA packaging protein during phage infection. |
+ | This part confers resistance against T7 phage upon a strain containing the Cas9 and sgRNA parts. | ||
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | <b>This part can be considered as an improvement of the <partinfo>BBa_K1129012</partinfo></b>, as they contain same N20 sequence but different sgRNA sequence. We fused crRNA and tracrRNA as a single synthetic guide RNA (sgRNA), while UBC iGEM 2013 constructed crRNA (repeat-spacer array) and tracrRNA separately. In their construct, the crRNA and tracrRNA were separately transcript, followed by the combination of these transcripts to form the sgRNA. The resist efficiency may decrease when the crRNA and tracrRNA not 100% match successfully. The way we constructed the sgRNA obviated the need for processing the transcribed CRISPR array (pre-crRNA) into individual crRNA components, helping to promote the function of resistance against T7 phage. | ||
+ | |||
+ | ===Gel analysis=== | ||
+ | [[File:BBa_K2325003--1.png|600px]] | ||
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Latest revision as of 11:59, 29 October 2017
T7 phage N20-sgRNA
The BBa_K2325003 is a DNA sequence contains N20 associated with sgRNA. The N20 is selected from the genome of T7 phage, which is responsible for the synthesis of the DNA packaging protein during phage infection. This part confers resistance against T7 phage upon a strain containing the Cas9 and sgRNA parts.
Usage and Biology
This part can be considered as an improvement of the BBa_K1129012, as they contain same N20 sequence but different sgRNA sequence. We fused crRNA and tracrRNA as a single synthetic guide RNA (sgRNA), while UBC iGEM 2013 constructed crRNA (repeat-spacer array) and tracrRNA separately. In their construct, the crRNA and tracrRNA were separately transcript, followed by the combination of these transcripts to form the sgRNA. The resist efficiency may decrease when the crRNA and tracrRNA not 100% match successfully. The way we constructed the sgRNA obviated the need for processing the transcribed CRISPR array (pre-crRNA) into individual crRNA components, helping to promote the function of resistance against T7 phage.
Gel analysis
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]