Team:Caltech/week13
From 2014.igem.org
(Difference between revisions)
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<b>lamBCDA & fsrABC Reception Systems</b> | <b>lamBCDA & fsrABC Reception Systems</b> | ||
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<b>Export Systems</b> | <b>Export Systems</b> | ||
- | <ul> | + | <br>Preparation of fsr system for LC/MS analysis: |
+ | <ul><li>Made new LB-CARB plates, since the old stock had run out.</li> | ||
+ | <li>Transformed pTG005-unFLAG into DH5α. Cells were plated & incubated overnight.</li> | ||
</ul> | </ul> | ||
<b>lamBCDA & fsrABC Reception Systems</b> | <b>lamBCDA & fsrABC Reception Systems</b> | ||
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<b>Export Systems</b> | <b>Export Systems</b> | ||
- | <ul> | + | <br>Preparation of fsr system for LC/MS analysis: |
+ | <ul><li>Set up a liquid culture of pTG005-unFLAG cells.</li> | ||
</ul> | </ul> | ||
<b>lamBCDA & fsrABC Reception Systems</b> | <b>lamBCDA & fsrABC Reception Systems</b> | ||
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<b>Export Systems</b> | <b>Export Systems</b> | ||
- | <ul> | + | <br>Preparation of fsr system for LC/MS analysis: |
+ | <ul><li>Set up 0 nM, 250 nM, & 500 nM aTc inductions of pTG005-unFLAG expressing cells in MOPS media. 5 μL aliquots of last night's liquid culture was used to start each culture.</li> | ||
</ul> | </ul> | ||
<b>lamBCDA & fsrABC Reception Systems</b> | <b>lamBCDA & fsrABC Reception Systems</b> | ||
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<b>Export Systems</b> | <b>Export Systems</b> | ||
- | <ul> | + | <br>Preparation of fsr system for LC/MS analysis: |
+ | <ul><li>aTc-induced MOPS liquid cultures from yesterday were spun down, and then the supernatant was loaded into C18 columns, washed with 10% acetonitrile, and then eluted with 60% acetonitrile.</li> | ||
</ul> | </ul> | ||
<b>lamBCDA & fsrABC Reception Systems</b> | <b>lamBCDA & fsrABC Reception Systems</b> |
Revision as of 01:29, 15 September 2014
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