21 May 2008

From 2008.igem.org

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'''Volunteers Scheduled for Today'''
 
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5-8 AS<br>
 
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6-8 DL<br>
 
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'''Things to do''':<br>
 
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<strike>Mini-preps of O/N's</strike><br>
 
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Sequence gel purified fragments from yesterday<br>
 
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Transform I0500<br>
 
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<strike>Digest J61003 with Xba/Pst to insert ORF's</strike><br>
 
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<strike>Digest minipreps with Xba/Pst to insert into J61003</strike><br>
 
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Run gel of digests and excise correct fragments<br>
 
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Ligate vector/inserts<br>
 
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Transform ligation reactions<br>
 
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Lab clean up<br>
 
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<u>'''James'''</u>:<br>
 
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<ul><li>Checked all O/N's set up by SZ and WX - all grew except 023 WX.  Will set up again tonight.<br>
 
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<li>Followed standard Qiagen miniprep protocol for all o/n's.</ul><br>
 
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<u>'''Winnie''' and '''Saima'''</u>:
 
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<ul><li>Digested J61003 using Xba and Pst
 
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<li>Digested minipreps of last year's genes using Xba and Pst
 
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<li>Began sequencing the o/n minipreps</ul>
 
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==The Good and Bad news==
 
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<u>'''The Good News'''</U><br>
 
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Our system will work in E.coli<br>
 
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<u>'''The Bad News'''</U><br>
 
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In 2004 Texas submitted the cyanbacterial equivalent of our system, so... Our biobricks would be unique but they would do the exact same thing.<br>
 
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<u>'''The Good News'''</U><br>
 
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I looked up a very promising pathway that detects blue light instead<br>
 
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<u>'''The Bad News'''</U><br>
 
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I can only find a summary of the paper... Here is the link to it
 
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http://www.arabidopsis.org/servlets/TairObject?type=publication&id=501724582
 
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==Lab Tip of the Day==
 
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When using the NanoVu to measure your DNA concentration, please ensure that you press the ''measure'' button and not the ''calibration'' button. Also, remember that the instructions for using the NanoVu are posted above the NanoVu. Please refer to these instructions in times of doubt instead of getting Chris to do it for you.
 
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PS: Falafel does not a good pizza make.
 
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==For your Consideration==
 
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'''Sound Emitting Bacteria'''
 
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http://www.jstage.jst.go.jp/article/jgam/44/1/44_49/_article
 

Latest revision as of 19:20, 22 May 2008