Difference between revisions of "Team:Lambert GA/Experiments"

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<div id="subheading1"><b>Wet Lab Summary</b><div>
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<h1>Experiments</h1>
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<p>Describe the research, experiments, and protocols you used in your iGEM project. These should be detailed enough for another team to repeat your experiments.</p>
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<div id="subheading1"><b>Work Flow</b><div>
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Please remember to put all characterization and measurement data for your parts on the corresponding Registry part pages.
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<li style="font-size:20px;">Miniprep/Nanodrop</li>
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<li style="font-size:20px;">Digest </li>
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<li style="font-size:20px;">Gel </li>
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<li style="font-size:20px;">Ligation</li>
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<li style="font-size:20px;">Transformation/electroporation, Plate </li>
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<li style="font-size:20px;">Colony PCR (Screening) </li>
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<li style="font-size:20px;">Gel</li>
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<li style="font-size:20px;">Inoculate correct colony to a liquid culture</li>
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<li style="font-size:20px;">Miniprep/Nanodrop</li>
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<li style="font-size:20px;">Sequence</li>
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<a href="https://www.facebook.com/groups/198318606966726/"><i class="fa fa-facebook" id="flogo"></i></a>
  
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<h3>What should this page contain?</h3>
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<li> Protocols </li>
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<li> Experiments </li>
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<li> Documentation of the development of your project </li>
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<h3>Inspiration</h3>
 
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<li><a href="https://2014.igem.org/Team:Colombia/Protocols">2014 Colombia </a></li>
 
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<li><a href="https://2014.igem.org/Team:Imperial/Protocols">2014 Imperial </a></li>
 
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<li><a href="https://2014.igem.org/Team:Caltech/Project/Experiments">2014 Caltech </a></li>
 
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Revision as of 00:30, 15 October 2018

CALM ELECTROPEN
BACKGROUND DATA & METHODS RESULTS DISCUSSION COLOR Q SUPPLEMENTARY REFERENCES
COLOR Q CHROME Q REFERENCES
PRINCIPLES & DESIGN MODEL & THEORY PRODUCT DESIGN REFERENCES
INTEGRATED HUMAN PRACTICES EDUCATION & ENGAGEMENT COLLABORATIONS
BASIC PARTS COMPOSITE PARTS
DESCRIPTION BACKGROUND DESIGN EXPERIMENTS LAB NOTEBOOK INTERLAB RESULTS DEMONSTRATE THE VISION
TEAM MEMBERS ATTRIBUTIONS
E X P E R I M E N T S



































Wet Lab Summary


Gaurav add wet lab summary
Work Flow


  1. Miniprep/Nanodrop
  2. Digest
  3. Gel
  4. Ligation
  5. Transformation/electroporation, Plate
  6. Colony PCR (Screening)
  7. Gel
  8. Inoculate correct colony to a liquid culture
  9. Miniprep/Nanodrop
  10. Sequence