Difference between revisions of "Part:BBa K3718003"
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<h1>crRNA</h1> | <h1>crRNA</h1> | ||
− | Through the results returned by CHOPCHOP, our team selected the crRNA at rank no.2, which is positioned at about one-fifth into the<I>arcA</I> gene. The <I>arcA</I> protein is expected to be dysfunctioned. The CG content is 40% and its efficiency is predicted at 70.41%. | + | Through the results returned by CHOPCHOP, our team selected the crRNA at rank no.2, which is positioned at about one-fifth into the <I>arcA</I> gene. The <I>arcA</I> protein is expected to be dysfunctioned. The CG content is 40% and its efficiency is predicted at 70.41%. |
<h1>tracrRNA and T7 terminator</h1> | <h1>tracrRNA and T7 terminator</h1> |
Latest revision as of 15:34, 18 October 2021
sgRNA for arcA with terminator - transcription template
Single guide RNA targeting arcA, for knock-out
crRNA
Through the results returned by CHOPCHOP, our team selected the crRNA at rank no.2, which is positioned at about one-fifth into the arcA gene. The arcA protein is expected to be dysfunctioned. The CG content is 40% and its efficiency is predicted at 70.41%.
tracrRNA and T7 terminator
The design of tracrRNA and T7 terminator is referenced from the 2017 IGEM team iGEM17_BGIC-Union, part BBa_K2371006.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 1
Illegal suffix found in sequence at 171 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 1
Illegal SpeI site found at 172
Illegal PstI site found at 186
Illegal NotI site found at 7
Illegal NotI site found at 179 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 1
- 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 1
Illegal suffix found in sequence at 172 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 1
Illegal XbaI site found at 16
Illegal SpeI site found at 172
Illegal PstI site found at 186 - 1000COMPATIBLE WITH RFC[1000]