Difference between revisions of "Part:BBa K2909010"
Laurent CHEN (Talk | contribs) |
|||
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
− | <partinfo> | + | <partinfo>BBa_K29090010 short</partinfo> |
− | |||
− | |||
− | |||
− | |||
− | |||
− | |||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K2909010 SequenceAndFeatures</partinfo> | <partinfo>BBa_K2909010 SequenceAndFeatures</partinfo> | ||
− | + | =='''Introduction'''== | |
− | == | + | |
− | < | + | <h3> 1- Biological background </h3> |
− | + | ||
+ | This part is a CDS coding for the E. guineensis LPAAT-A enzyme tagged with a C-terminal HiBiT tag under the control of a nitrate-inducible Chlamydomonas reinhardtii promoter called NIT1. It also contains a Hygromycin resistance cassette called AphVII to select the recombinant clones.<br> | ||
+ | |||
+ | This part has been designed to characterize the expression of the E. guineensis LPAAT-A enzyme that we adapted for C. reinhardtii (BBa_K2909002) with the C-terminal HibiT tag.<br> | ||
+ | |||
+ | This part is a linear DNA that is the result of the digestion of the level M plasmid by the type IIS BsaI restriciton enzyme. It is this linear DNA that is integrated into the genomic DNA of Chlamydomonas reinhardtii during the transformation. | ||
+ | |||
+ | <h3> 2- Usage in iGEM projects </h3> | ||
+ | |||
+ | Bio[oil]gical Factory (iGEM Sorbonne Université 2019) |
Revision as of 15:09, 28 August 2019
No part name specified with partinfo tag.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 5
Illegal EcoRI site found at 2494
Illegal PstI site found at 1233 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 5
Illegal EcoRI site found at 2494
Illegal NheI site found at 2758
Illegal PstI site found at 1233
Illegal NotI site found at 217 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 5
Illegal EcoRI site found at 2494
Illegal BamHI site found at 1075
Illegal XhoI site found at 758 - 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 5
Illegal EcoRI site found at 2494
Illegal PstI site found at 1233 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 5
Illegal EcoRI site found at 2494
Illegal PstI site found at 1233
Illegal NgoMIV site found at 1788
Illegal NgoMIV site found at 3459
Illegal NgoMIV site found at 3641 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1965
Introduction
1- Biological background
This part is a CDS coding for the E. guineensis LPAAT-A enzyme tagged with a C-terminal HiBiT tag under the control of a nitrate-inducible Chlamydomonas reinhardtii promoter called NIT1. It also contains a Hygromycin resistance cassette called AphVII to select the recombinant clones.
This part has been designed to characterize the expression of the E. guineensis LPAAT-A enzyme that we adapted for C. reinhardtii (BBa_K2909002) with the C-terminal HibiT tag.
This part is a linear DNA that is the result of the digestion of the level M plasmid by the type IIS BsaI restriciton enzyme. It is this linear DNA that is integrated into the genomic DNA of Chlamydomonas reinhardtii during the transformation.
2- Usage in iGEM projects
Bio[oil]gical Factory (iGEM Sorbonne Université 2019)