Difference between revisions of "Part:BBa K2404005"
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<partinfo>BBa_K2404005 short</partinfo> | <partinfo>BBa_K2404005 short</partinfo> | ||
− | + | The [https://apps.araport.org/thalemine/report.do?id=69089924&trail=|69089924 WRKY30 promotor] is a regulatory sequence from <i>Arabidopsis thaliana</i> that has been characterised as a [http://www.plantphysiol.org/content/early/2017/02/27/pp.16.01680 ‘Damage Associated Molecular Patterns’ (DAMP)]. | |
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+ | This promotor is situated -653 > -168 upstream of the WRKY30 translational start point. | ||
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+ | This part conforms to the [http://2016.igem.org/Resources/Plant_Synthetic_Biology/PhytoBricks Phytobrick] standard and contains the 5' GGAG and 3' AATG sequences for cloning into level 1 plasmids. | ||
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+ | This part is has been cloned into the [https://parts.igem.org/Part:BBa_P10500 P10500] plasmid using BsmBI. | ||
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<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
− | <partinfo> | + | <partinfo>BBa_K2404005 SequenceAndFeatures</partinfo> |
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===Functional Parameters=== | ===Functional Parameters=== | ||
− | <partinfo> | + | <partinfo>BBa_K2404005 parameters</partinfo> |
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Latest revision as of 21:25, 30 October 2017
WRKY30 - a promoter induced by the presence of cellulose-derived oligomers
The WRKY30 promotor is a regulatory sequence from Arabidopsis thaliana that has been characterised as a [http://www.plantphysiol.org/content/early/2017/02/27/pp.16.01680 ‘Damage Associated Molecular Patterns’ (DAMP)].
This promotor is situated -653 > -168 upstream of the WRKY30 translational start point.
This part conforms to the [http://2016.igem.org/Resources/Plant_Synthetic_Biology/PhytoBricks Phytobrick] standard and contains the 5' GGAG and 3' AATG sequences for cloning into level 1 plasmids.
This part is has been cloned into the P10500 plasmid using BsmBI.
Sequence and Features
Assembly Compatibility:
- 10INCOMPATIBLE WITH RFC[10]Illegal XbaI site found at 122
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23INCOMPATIBLE WITH RFC[23]Illegal XbaI site found at 122
- 25INCOMPATIBLE WITH RFC[25]Illegal XbaI site found at 122
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 1
Illegal BsaI site found at 477
Illegal BsaI.rc site found at 502