Difference between revisions of "Team:CIEI-BJ/Medals"

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<div class="second-level" id="a7" >Laminar Flow</div>
 
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<img class="my-img" src="https://static.igem.org/mediawiki/2017/b/bc/T--CIEI-BJ--Safety--fingure4.jpg" />
 
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<p class="my-content" >A laminar flow is an enclosed, ventilated chamber which contains UV light to kill the bacteria when not using it. Common rules about using it includes: completely sterilize your glove using 70% alcohol, turn off the UV lights when putting your hands in and avoid letting your unsterilized sleeves or watches touch the samples. Everyone must be familiar with the rules before they operate in a laminar flow.</p>
 
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<div class="second-level" id="a8" >Weighing Scale</div>
 
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<img class="my-img" src="https://static.igem.org/mediawiki/2017/5/51/T--CIEI-BJ--Safety--fingure5.jpg" />
 
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<p class="my-content" >Weighing scale are devices which are used to weigh the mass of some matters. It can correct the measurement to0.01g. And before we measure the weight, we need pave a paper firstly, and then place the matter on the paper,because it can protect the matter from the wind or touching.</p>
 
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<div class="second-level" id="a9" >Gel Documentation System</div>
 
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<img class="my-img" src="https://static.igem.org/mediawiki/2017/5/5a/T--CIEI-BJ--Safety--fingure6.jpg" />
 
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<p class="my-content" >The gel documentation system is a huge machine that can test the trace of nucleic acid left in gel electrophoresis by exposing the whole gel to UV light. The samples are often mixed with SYBR (color).</p>
 
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<div class="second-level" id="a10" >Gel Electrophoresis Equipment</div>
 
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<img class="my-img" src="https://static.igem.org/mediawiki/2017/3/3c/T--CIEI-BJ--Safety--fingure7.jpg" />
 
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<p class="my-content" >Gel Electrophoresis Equipment is a machine which processes the Gel Electrophoresis. We put the gel which take the DNA and add the 1xTEA. Then we power on it. The DNA start moving from negative charge to positive charge. Because of that, we can check out the DNA whether we need. Used safe florescence dye instead of the toxic EB, wear two layers of glove, processed in specialized area, all of the waste produced were treated individually.</p>
 
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<div class="second-level" id="a11" >Water bath</div>
 
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<img class="my-img" src="https://static.igem.org/mediawiki/2017/a/a3/T--CIEI-BJ--Safety--fingure8.jpg" />
 
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<p class="my-content" >Water bath can keep a constant temperature for incubation or E.coli the water. So we can do some work which need at a high constant temperature. For example, the transformation, we put the vector and fragment on the buoy and drop into the water, then they can start transform in the best constant temperature. Furthermore, if we want to save a matter recently in a constant temperature, we also can use it. Make sure there is always water in the water bath, avoid dry heating and burning.</p>
 
 
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Revision as of 11:27, 4 October 2018

Top
Bronze

Competition deliverables

wiki

poster

presentation

judging form



Attribution



Contribution

Complete the inter-lab measurement study (submit online)



complete safety form

Silver (add based on the brozne criteria

Validated part

at least one new bio-brick part is related to our project work.

submit a sample of this part

follow all of the DNA Submission Requirements and Shipping Guidelines



Collaboration

worked with one currently registered 2018 iGEM teams

document your collboration in detail on your wiki



Human practices

convince the judges that your work is responsible and good for the world

document on the team wiki

Gold (added based on the silver criteria

Integrated human practices

expand on silver medal activity



Improve a previous part

New bio-brick has a