Team:NYMU-Taipei/notebook/labnotes
From 2014.igem.org
(Difference between revisions)
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<li>In the checking step, we’ve have contaminated electrophoresis result after colony PCR. That is, we got band in the negative well. To find out the ingredient causing contamination, we do several negative control changing different packing of ingredients. And find the contamination of our 10X DreamTaq Buffer.</li> | <li>In the checking step, we’ve have contaminated electrophoresis result after colony PCR. That is, we got band in the negative well. To find out the ingredient causing contamination, we do several negative control changing different packing of ingredients. And find the contamination of our 10X DreamTaq Buffer.</li> | ||
</ol> | </ol> | ||
+ | <h3>Result</h3> | ||
+ | <img src='/wiki/images/4/43/NYMU14_note_4c_r1.PNG'> | ||
+ | <img src='/wiki/images/f/ff/NYMU14_note_4c_r2.PNG'> | ||
+ | <img src='/wiki/images/a/a3/NYMU14_note_4c_r3.PNG'> | ||
+ | <img src='/wiki/images/c/cd/NYMU14_note_4c_r4.PNG'> | ||
+ | <img src='/wiki/images/e/eb/NYMU14_note_4c_r5.PNG'> | ||
</div> | </div> | ||
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Revision as of 18:14, 28 September 2014
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introduction
control
communication
cohesion
completion
function test
introduction :P introduction :P introduction :P introduction :P
introduction of labnote
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