Difference between revisions of "Team:Bio Without Borders/Notebook"

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</ul>
 
</ul>
  
<h3>Using DNA distribution kit plates: Rehydration of registry DNA from kit plate</h3>
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<h2>Using DNA distribution kit plates: Rehydration of registry DNA from kit plate</h2>
 
<p>Wells in the DNA distribution kit plates contain 2-3 ng of dry DNA. This should be enough DNA for a few transformation, but insufficient for immediate restriction and ligation.</p>
 
<p>Wells in the DNA distribution kit plates contain 2-3 ng of dry DNA. This should be enough DNA for a few transformation, but insufficient for immediate restriction and ligation.</p>
  
 +
<h4>Materials</h4>
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<ul style="list-style-type:disc;">
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<li>DNA distribution kit plates</li>
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<li>Sterile distilled water</li>
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<li>Micropipette</li>
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<li>Sterile micropipette tip</li>
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</ul>
 
<h4>Protocol</h4>
 
<h4>Protocol</h4>
  

Revision as of 20:07, 25 September 2019

Notebook

Document the dates you worked on your project. This should be a detailed account of the work done each day for your project.

What should this page have?

  • Chronological notes of what your team is doing.
  • Brief descriptions of daily important events.
  • Pictures of your progress.
  • Mention who participated in what task.

Using DNA distribution kit plates: Rehydration of registry DNA from kit plate

Wells in the DNA distribution kit plates contain 2-3 ng of dry DNA. This should be enough DNA for a few transformation, but insufficient for immediate restriction and ligation.

Materials

  • DNA distribution kit plates
  • Sterile distilled water
  • Micropipette
  • Sterile micropipette tip

Protocol

  1. Locate the well with the DNA part you need
  2. Using a micro pipette, draw 10 μL sterile distilled water into a sterile pipette tip
  3. Use the pipette tip to puncture a hole through the cover foil and into the well containing DNA you need.
  4. Release the water into the well and pipette up and down a few times to rehydrate the DNA you need
  5. Store the re-hydrated DNA in the -20C freezer. You can either leave it in the original plate, or transfer it into a separate tube (make sure to label the tube!).
  6. The rehydrated DNA can be used immediately to transform competent cells. As little as 1 μL should be enough for one transformation.

Inspiration

You can see what others teams have done to organize their notes: