Team:Bordeaux/NotebookJune23

From 2014.igem.org

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(Created page with "{{:Team:Bordeaux/Tete}} <html> <h1>19<sup>th</sup> June </h1> <div class="type-exp"> Molecular biology</div> <br> <ul class="day-detail"> <li>PCR of ELP-40 and ELP-60<br> <div...")
 
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<html>
<html>
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<h1>19<sup>th</sup> June </h1>
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<h1>23<sup>rd</sup> June </h1>
<div class="type-exp"> Molecular biology</div>
<div class="type-exp"> Molecular biology</div>
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<ul class="day-detail">
<ul class="day-detail">
<li>PCR of ELP-40 and ELP-60<br>
<li>PCR of ELP-40 and ELP-60<br>
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<div style="margin-left:95px ;"> => Dilution primer 100µM => 10µM
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<div style="margin-left:85px ;"> => Dilution primer 100µM => 10µM<br>
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Primer forward: 1µl primer + 9µl H2O (Tm=58°C)
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Primer forward: 1µl primer + 9µl H2O (Tm=58°C)<br>
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Primer reverse: 1µl primer + 9µl H2O (Tm=68°C)</div><br>
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Primer reverse: 1µl primer + 9µl H2O (Tm=68°C)</div>
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<br>
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Test of different hybridation temperature for PCR: 59°C 61°C 63°C 65°C 68°C <br>
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Test of different hybridation temperature for PCR: 59°C 61°C 63°C 65°C 68°C <br><br>
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Mix for 11 tubes</li><br>
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Mix for 11 tubes<br>
<table>
<table>
   <tr>
   <tr>
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     <td>dNTP</td>
     <td>dNTP</td>
     <td>11µl</td>  
     <td>11µl</td>  
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   </tr>
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   </tr>
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</table><br>
</table><br>
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<div style="margin-left:65px ;">
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Thermal cycler : <br>
Thermal cycler : <br>
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<div style="margin-left:95px ;">
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<div style="margin-left:70px ;">
3min 95°C<br>
3min 95°C<br>
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30sec 95°C </div><br>
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25 cycles : 30sec 95°C <br><div style="margin-left:70px ;"> 30sec at all temperatures tested<br>
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25 cycles
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3sec 72°C<br></div>
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<div style="margin-left:95px ;">  
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-
30sec at all temperatures tested<br>
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3sec 72°C<br>
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5min 72°C</div>
5min 72°C</div>
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</div>
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</li>
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<br>
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<ul class="day-detail">
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<br><br>
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<li>Digestion cloning 1 (psB6A1) miniprep of 10/06/14 and VPGXG-20 (PCR of 10/06/14)<br>
<li>Digestion cloning 1 (psB6A1) miniprep of 10/06/14 and VPGXG-20 (PCR of 10/06/14)<br>
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   <tr>
   <tr>
     <th>DNA</th>
     <th>DNA</th>
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     <td>10µl</td>
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     <td>10µl (*)</td>
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     <td>10µl</td>
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     <td>10µl (**)</td>
   </tr>
   </tr>
</table>
</table>
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</ul>
 
<br>
<br>
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With DNA = 6μl vector + 4μl H2O <br>
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(*) With DNA = 6μl vector + 4μl H2O <br>
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With DNA= 0.56μl Miniprep product + 9,44μl H2O</li>
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(**) With DNA= 0.56μl Miniprep product + 9,44μl H2O</li><br><br>
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<li>Digestion vector psB6A1 :
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<li>Digestion vector psB6A1 : <br>
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<img style="margin-left:20px;" src="https://static.igem.org/mediawiki/2014/b/bd/Math1.PNG" alt=math1><br><br>
<table>
<table>

Latest revision as of 00:16, 18 October 2014

23rd June

Molecular biology

  • PCR of ELP-40 and ELP-60
    => Dilution primer 100µM => 10µM
    Primer forward: 1µl primer + 9µl H2O (Tm=58°C)
    Primer reverse: 1µl primer + 9µl H2O (Tm=68°C)

    Test of different hybridation temperature for PCR: 59°C 61°C 63°C 65°C 68°C

    Mix for 11 tubes
    H2O 357,5 µl
    Buffer 5X 110 µl
    Primer 27,5 µl
    dNTP 11µl

    Thermal cycler :
    3min 95°C
    25 cycles : 30sec 95°C
    30sec at all temperatures tested
    3sec 72°C
    5min 72°C


  • Digestion cloning 1 (psB6A1) miniprep of 10/06/14 and VPGXG-20 (PCR of 10/06/14)
    Digestion plasmid Digestion insert
    H2O 7,5µl 7,5µl
    10X buffer 4 2µl 2µl
    XbaI 0,25µl 0,25µL
    EcoRI 0,25µl 0,25µl
    DNA 10µl (*) 10µl (**)

    (*) With DNA = 6μl vector + 4μl H2O
    (**) With DNA= 0.56μl Miniprep product + 9,44μl H2O


  • Digestion vector psB6A1 :
    math1

    Digestion plasmid
    H2O 7,5µl
    10X buffer 4 2µl
    XbaI 0,25µl
    EcoRI 0,25µl
    DNA 10µl

  • Digestion psB1C3 and PCR 40 and 60
    OD PCR tube 40= 282,5 ng/μl
    OD PCR tube 60= 366,3 ng/μl
    Tube 40 = 0,88 DNA +9,12µl H2O
    Tube 60 = 2,5 DNA + 7,5 µl H2O


  • Production
    We want to do a preculture test to have a better production.