Difference between revisions of "Team:Carnegie Mellon/Protocols"

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     $("#flip_ligation").click(function(){
 
     $("#flip_ligation").click(function(){
 
         $("#ligation_p").slideToggle("slow");
 
         $("#ligation_p").slideToggle("slow");
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    });
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});
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$(document).ready(function(){
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    $("#flip_transformation").click(function(){
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        $("#transformation_p").slideToggle("slow");
 
     });
 
     });
 
});
 
});
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#ligation_p {
 
#ligation_p {
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    padding: 30px;
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    display: none;
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    background-color: transparent;
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    width: 76%;
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    margin-left: auto;
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    text-align: left;
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    color: black;
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}
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#transformation_p, #flip_transformation {
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    padding: 5px;
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    text-align: center;
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    border: solid 3px #c3c3c3;
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    background-color: #40e6ee; /* #69c94f; */
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    color: white;
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    width: 80%;
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    margin: auto;
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}
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#transformation_p {
 
     padding: 30px;
 
     padding: 30px;
 
     display: none;
 
     display: none;
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</div><!-- ligation_p -->
 
</div><!-- ligation_p -->
  
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<!-- __________________________ Transformation Protocol _____________ -->
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<div id = "flip_transformation">Transformation</div>
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<div id = "transformation_p">
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<div class = "title">Transformation</div>
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<div class = "procedure">Procedure:</div>
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<ol>
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<li>Follow <a href = "http://parts.igem.org/Help:Protocols/Transformation">iGEM's Transformation Protocol</a></li>
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</ol>
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</div><!-- transformation_p -->
  
 
</body>
 
</body>
  
 
</html>
 
</html>

Revision as of 20:01, 10 August 2015

Under Construction.

This is almost as well-documented as Kim Kardashian's wedding.

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His-Tag Soluble Protein Extraction
  1. Centrifuge 1.5 ml of culture for 1min full speed at 15000 rpm.
  2. Remove supernatant.
  3. Add 250 µl of extraction buffer (1% octyl-beta-thioglucoside in 10mM Tris-Cl, pH7.5).
  4. Incubate at room temperature for 10 min.
Wash Beads
  1. Remove 50 µl of Ni-NTA in 10 mM Trischloride bead solution and place in new tube for each purification.
  2. Add 1 mL buffer (see table).
  3. Centrifuge at 800 rpm for 30 seconds.
  4. Remove supernatant.
  5. Repeat 3 times and resuspend in 1 mL of Bead Wash Solution.
Estrogen Sensor
Estrogen Sensor Protocol
MiniPrep
Minipreps of MACH Cells Expressing Flourescence
Purpose: To isolate plasmid DNA from MACH cells.

Procedure:

  1. Set up overnight cultures for miniprep.
  2. Make the following reaction recipe:
    • 5 mL LB
    • 5 µL Chlorophenical
    • 1 µL overnight colony
  3. Incubate in 37°C for 16-18 hours.
  4. Follow the Life Technologies Miniprep Kit Protocol.
Restriction Enzyme Digestl
Restriction Enzyme Digest
Procedure:
  1. Prepare the following restriction enzyme digestion solution for J23108, J23109, J23111.
    2. Reagent Amount (µL)
    10X Fast Digest Buffer 2
    Plasmid DNA 12
    Restriction Enzyme XbaI 1
    Restriction Enzyme SpeI 1
    Water (to bring up to volume) 2
    Total Volume 18
  2. Digest at 37 °C for 1 hour.
  3. Follow the Life Technologies Restriction Enzyme Digest Protocol.
Agarose Gel Electrophoresis
Aragose Gel Electrophoresis
Procedure:
  1. 1% aragose gel made of:
      50 mL 0.5X TAE
      0.5g agarose
      2.5 µL ethidium bromide
  2. Run at 114V.
Gel Extraction
Gel Extraction
Procedure:
  1. Make 250-750 µl binding buffer (depending on mass of gel cut-out).
  2. Incubated at 42℃ until gel is melted.
  3. Follow Thermo Scientific's GeneJET Gel Extracton Protocol
Ligation
Ligation
Procedure:
  1. Make the following ligation reaction.
    2. Reagent Amount (µL)
    Promoter DNA 1
    Insert DNA 7
    Ligation Buffer 1
    Ligation Enzyme 1
    Total Volume 10
  2. Ligate for 10 minutes at room temperature.
  3. Put on ice until ready for transformation.
Transformation
Transformation
Procedure:
  1. Follow iGEM's Transformation Protocol