Team:Exeter/lab book/gibs/wk9
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- | <a href="https://2012.igem.org/Team:Exeter/ | + | <a href="https://2012.igem.org/Team:Exeter/Results#usepoly"; style="color:#e30614" target="_blank"><font size="3"><b>Results: Part 1</b></font></a> |
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- | <a href="https://2012.igem.org/Team:Exeter/ | + | <a href="https://2012.igem.org/Team:Exeter/Results/GvsB"; style="color:#e30614" target="_blank"><font size="3"><b>Results: Part 2</b></font></a> |
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<!------------INSERT WEEKLY IMAGE HERE------------> | <!------------INSERT WEEKLY IMAGE HERE------------> | ||
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<p><b><u>Operon Construction: 3rd - 7th September 2012</u></b></p> | <p><b><u>Operon Construction: 3rd - 7th September 2012</u></b></p> | ||
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<p>Gibson PCR again</p><p> | <p>Gibson PCR again</p><p> | ||
Fragments and concentrations as 30.8.12</p><p> | Fragments and concentrations as 30.8.12</p><p> | ||
- | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/12" style="color:# | + | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/12" style="color:#57b947"><u>3 step PCR</u></a></p><p> |
- | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:# | + | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>Two step PCR</u></a></p><br><p> |
PCR setup: </p><p> | PCR setup: </p><p> | ||
98 °C for 30s</p><p> | 98 °C for 30s</p><p> | ||
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<b>**Tuesday 4.9.12**</b></p><br><p> | <b>**Tuesday 4.9.12**</b></p><br><p> | ||
Mega-miniprep day: Due to various iGEM commitments, an overwhelming number of minipreps was required. LB broth was inoculated 3.9.12 - Four colonies from each plate from all transformations from 21.08.12 onwards were put in broth and miniprepped (see Freddie’s lab book for 3 gene inducible plasmid for details) </p><p> | Mega-miniprep day: Due to various iGEM commitments, an overwhelming number of minipreps was required. LB broth was inoculated 3.9.12 - Four colonies from each plate from all transformations from 21.08.12 onwards were put in broth and miniprepped (see Freddie’s lab book for 3 gene inducible plasmid for details) </p><p> | ||
- | <p>Miniprep according to<ahref="http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:#57B947" target="_blank"><u>Fermentas protocol</u></a></p> | + | <p>Miniprep according to <ahref="http://www.fermentas.com/templates/files/tiny_mce/coa_pdf/coa_k0502.pdf" style="color:#57B947" target="_blank"><u>Fermentas protocol</u></a></p> |
<p><b>**Wednesday 5.9.12**</b></p><br><p> | <p><b>**Wednesday 5.9.12**</b></p><br><p> | ||
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- | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/12" style="color:# | + | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/12" style="color:#57b947"><u>3 step PCR</u></a></p><p> |
- | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:# | + | <a href="https://2012.igem.org/Team:Exeter/lab_book/proto/7" style="color:#57b947"><u>2 step PCR</u></a></p><br><p> |
PCR setup: </p><p> | PCR setup: </p><p> | ||
98 °C for 30s</p><p> | 98 °C for 30s</p><p> | ||
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Hold temp. 4 °C</p><br><p> | Hold temp. 4 °C</p><br><p> | ||
- | <b>**Friday 7.9.12**<b></p><br><p> | + | <b>**Friday 7.9.12**</b></p><br><p> |
Ran gel from previous PCR – <i>wbbC</i> worked (although significant blurring – fewer PCR steps may have helped.) </p><p> | Ran gel from previous PCR – <i>wbbC</i> worked (although significant blurring – fewer PCR steps may have helped.) </p><p> | ||
Gibson PCR of Pbad, <i>wbnJ</i> and <i>wbnK</i> 2 using immomix red again</p><p> | Gibson PCR of Pbad, <i>wbnJ</i> and <i>wbnK</i> 2 using immomix red again</p><p> | ||
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+ | <font color="#57B947" size="1" face="Verdana"> | ||
+ | <p><u>Website Designed and Built by: Ryan Edginton, James Lynch & Alex Clowsley</u> | | ||
+ | <a href="https://igem.org/Team.cgi?id=764" style="color:#57B947" target="_blank"><u>Contact Us</u></a> | | ||
+ | <a href="https://2012.igem.org/Team:Exeter/site_map" style="color:#57B947"><u>Site Map</u></a></p> | ||
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+ | </tr> | ||
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Latest revision as of 00:11, 27 September 2012
Operon Construction: 3rd - 7th September 2012 **Monday 3.9.12**Gibson PCR again Fragments and concentrations as 30.8.12 PCR setup: 98 °C for 30s 98 °C for 10s, 69 °C for 30s, 72 °C for 20s – X 5 98 °C for 10s, 72 °C for 30s – X 25 72 °C for 10minutes Hold temp. 4 °C Ran gel – only wfcA 1 & 2 worked **Tuesday 4.9.12** Mega-miniprep day: Due to various iGEM commitments, an overwhelming number of minipreps was required. LB broth was inoculated 3.9.12 - Four colonies from each plate from all transformations from 21.08.12 onwards were put in broth and miniprepped (see Freddie’s lab book for 3 gene inducible plasmid for details)
Miniprep according to **Wednesday 5.9.12** Used nanodrop spectrophotometer to find concentrations from minipreps the previous day Gibson PCR of Pbad, wbnJ, wbbC and wbnK 2. DNA 1 µl, water 33 µl PCR setup: 98 °C for 30s 98 °C for 10s, 50 °C for 30s, 72 °C for 20s – X 5 98 °C for 10s, 72 °C for 30s – X 25 72 °C for 10 minutes Hold temp. 4 °C Gel run – no success **Thursday 6.9.12** Gibson PCR using Immomix red (2x). Pbad, wbnJ, wbbC, wbnK 2. Immomix red 25 µl DNA 1 µl Primer 1 – 2 µl Primer 2 – 2 µl Immomix red 2x – 25 µl Water - 20 µl PCR setup: 95 °C for 10 minutes 95 °C for 10s, 55 °C for 30s, 72 °C for 30s – X 25 Hold temp. 4 °C **Friday 7.9.12** Ran gel from previous PCR – wbbC worked (although significant blurring – fewer PCR steps may have helped.) Gibson PCR of Pbad, wbnJ and wbnK 2 using immomix red again Volumes as on 6.9.12 PCR setup: 95 °C for 10 minutes 95 °C for 10s, 65 °C for 30s, 72 °C for 30s – X 5 4 °C hold step Ran gel – no success |
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