Team:Exeter/lab book/3gip/wk6
From 2012.igem.org
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<p><i><b>Morning</b></i></p> | <p><i><b>Morning</b></i></p> | ||
- | <p>•<u> | + | <p>•<a href="http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:#57B947" target="_blank"><u>Miniprepping</u></a></p> |
<p>BBa_J13002 + <i>wbnK</i> BBa_B0014 in pSB1T3</p> | <p>BBa_J13002 + <i>wbnK</i> BBa_B0014 in pSB1T3</p> | ||
<p><i>wfcA</i> + BBa_B0014 in pSB1T3</p> | <p><i>wfcA</i> + BBa_B0014 in pSB1T3</p> |
Revision as of 21:36, 25 September 2012
The 3-Gene Inducible Plasmid: 13th - 17th August 2012 Monday 13th August See Operon Constructipn 13th - 17th August of RBS-wbbC(d) (BBa_B0034 + BBa_K764005) Tuesday 14th August See Operon Constructipn 13th - 17th August of RBS-wbbC(d) (BBa_B0034 + BBa_K764005) Wednesday 15th August Morning BBa_J13002 + wbnK BBa_B0014 in pSB1T3 wfcA + BBa_B0014 in pSB1T3 wbnJ + BBa_B0014 in pSB1T3 BBa_B0034 wbbC + BBa_B0014 in pSB1T3 Using the changed protocol. The tubes were centrifuged for 10 minutes to start to ensure a good pellet formed. After the neutralisation solution had been added, the eppendorfs were centrifuged for 10 minutes rather than 5 in order to get a better pellet formation. 40ul of water was added instead of 40ul in order to make sure the concentration of DNA increased. All were nanodropped and only wfcA + BBa_B0014 and wbnJ + BBa_B0014 gave good concentrations. Wednesday 15th August –Friday 17th August Preparation of presentation so no lab work. |