Difference between revisions of "Part:BBa K2278021"
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− | + | __NOTOC__ | |
+ | <partinfo>BBa_K2278011 short</partinfo> | ||
+ | |||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K2278011 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | =='''Introduction'''== | ||
+ | <html> | ||
+ | This DNA biobrick was designed in order to produce in <i></i> strain. | ||
+ | |||
+ | <h3 id="RT"> 1- Biological background </h3> | ||
+ | |||
+ | |||
+ | Mécanisme | ||
+ | |||
+ | <figure><p style="text-align:center;"> <img src ="g" width = "600" /> <figcaption> Figure 1: <btitre </b> figure caption</figcaption> </figure> | ||
+ | |||
+ | <h3 id="RT"> 2- Usage in iGEM projects </h3> | ||
+ | |||
+ | <p> The BBa_K2278011 cames from the module of the Croc’n cholera project <a href="http://2017.igem.org/Team:INSA-UPS_France">(team INSA-UPS-France 2017)</a> | ||
+ | It was designed to produce </p> | ||
+ | |||
+ | <p>The part includes </p> | ||
+ | |||
+ | |||
+ | </html> | ||
+ | |||
+ | |||
+ | |||
+ | =='''Experiments'''== | ||
+ | <html> | ||
+ | <h3 id="RT"> 1- Molecular biology </h3> | ||
+ | <p> | ||
+ | The gene was placed in silico under the control of the p promoter (BBa_R), a strong RBS (BBa_B0034) and a terminator (BBa_B1006). IDT performed the DNA synthesis and delivered the part as gBlock. | ||
+ | The construct was cloned by conventional ligation into pSB1C3 plasmid and transformed into E. coli Dh5 alpha strain. X transformants were obtained. | ||
+ | </p> | ||
+ | |||
+ | <b>Analysis of the restriction map </b> | ||
+ | |||
+ | <figure><p style="text-align:center;"><img src="" width = "600"/><figcaption> Figure 2: <b>title </b> Digested plasmids are electrophoresed through an 0.7% agarose gel. The desired plasmids lengths are in parentheses. pSB1C3 (2029bp the other band correspond to a xxx bp insert)</figcaption></figure> | ||
+ | |||
+ | <p><b>Sequencing </p></b> | ||
+ | |||
+ | <figure><p style="text-align:center;"><img src="" width = "500"/><figcaption> Figure 3: <b>Sequencing of pSB1C3_ </b> 1500 ng of plasmid are sequenced. X oligos were used to perform the sequencing. The obtained sequence were blast on the BBa_K2278011 sequence with the iGEM sequencing online tools. </figcaption></figure> | ||
+ | |||
+ | The sequencing show a | ||
+ | |||
+ | <h3 id="RT"> 2- Expression <i>in vivo</i> </h3> | ||
+ | <p><b>sous titre</b></p> | ||
+ | <p> Protocole </p> | ||
+ | |||
+ | |||
+ | </html> | ||
+ | =='''Characterization'''== | ||
+ | <html> | ||
+ | |||
+ | <h3 id="RT">1- Validation of </h3> | ||
+ | description | ||
+ | |||
+ | <p> <b>manip1 </b> </p> | ||
+ | |||
+ | Image stylée | ||
+ | |||
+ | <figure><p style="text-align:center;"><img src="" width = "500"/><figcaption> Figure <b>title </b>légende </figcaption></figure> | ||
+ | |||
+ | <p>Interprétation </p> | ||
+ | |||
+ | <p> <b>manip2</b> </p> | ||
+ | Image stylée | ||
+ | |||
+ | <figure><p style="text-align:center;"><img src="" width = "500"/><figcaption> Figure <b>plus de figure ! </figcaption></figure> | ||
+ | |||
+ | <p>interprétation </p> | ||
+ | |||
+ | <p><b>Discussion : </b> </p> | ||
+ | <p></p> | ||
+ | |||
+ | |||
+ | |||
+ | <h3 id="RT">2. 2ème approche </h3> | ||
+ | <figure><p style="text-align:center;"><img src="" width = "500"/><figcaption> Figure <b>Solid results </b> légende de qualité </figcaption></figure> | ||
+ | |||
+ | <p>brillante analyse</p> | ||
+ | |||
+ | <p><b>Discussion : </b> </p> | ||
+ | <p>des perspectives éclectiques </p> |
Revision as of 11:55, 10 October 2017
pTet driven Diacetyl generator (pTet + ALS)
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1738
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Introduction
This DNA biobrick was designed in order to produce in strain.
1- Biological background
Mécanisme2- Usage in iGEM projects
The BBa_K2278011 cames from the module of the Croc’n cholera project (team INSA-UPS-France 2017) It was designed to produce
The part includes
Experiments
1- Molecular biology
The gene was placed in silico under the control of the p promoter (BBa_R), a strong RBS (BBa_B0034) and a terminator (BBa_B1006). IDT performed the DNA synthesis and delivered the part as gBlock. The construct was cloned by conventional ligation into pSB1C3 plasmid and transformed into E. coli Dh5 alpha strain. X transformants were obtained.
Analysis of the restriction mapSequencing
The sequencing show a2- Expression in vivo
sous titre
Protocole
Characterization
1- Validation of
descriptionmanip1
Image styléeInterprétation
manip2
Image styléeinterprétation
Discussion :
2. 2ème approche
brillante analyse
Discussion :
des perspectives éclectiques