Team:Hannover/Notebook/Plant Vector

From 2014.igem.org

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<td>Lisa, Katharina </td>
<td>Lisa, Katharina </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>colony-PCR: only negative controls/ consultation of TR: modification of the protocol </td>
<td>colony-PCR: only negative controls/ consultation of TR: modification of the protocol </td>
</tr>
</tr>
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<td>Katharina </td>
<td>Katharina </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>plasmid isolation from ONC/ Digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells/ incubation over night (25 °C) </td>
<td>plasmid isolation from ONC/ Digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells/ incubation over night (25 °C) </td>
</tr>
</tr>
Line 54: Line 54:
<td>Katharina </td>
<td>Katharina </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>digestion of pORE-E3 (without XhoI- and BglII-site): no DNA: inoculation of an ONC </td>
<td>digestion of pORE-E3 (without XhoI- and BglII-site): no DNA: inoculation of an ONC </td>
</tr>
</tr>
Line 61: Line 61:
<td>Katharina, Björn </td>
<td>Katharina, Björn </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>colony-PCR with primer 1261 and 488: all 60 colonies negative: digestion probably went wrong/ isolation of plasmid of another ONC via handpreparation </td>
<td>colony-PCR with primer 1261 and 488: all 60 colonies negative: digestion probably went wrong/ isolation of plasmid of another ONC via handpreparation </td>
</tr>
</tr>
Line 68: Line 68:
<td>Katharina, Björn </td>
<td>Katharina, Björn </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>plasmid isolation from ONC/ digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells </td>
<td>plasmid isolation from ONC/ digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells </td>
</tr>
</tr>
Line 75: Line 75:
<td>Katharina, Björn </td>
<td>Katharina, Björn </td>
<td>IPG </td>
<td>IPG </td>
-
<td>insertion of rcf21 </td>
+
<td>insertion of RFC[21] </td>
<td>digestion of pORE-E3 (without XhoI and BglII-site): no DNA: inoculation of an ONC </td>
<td>digestion of pORE-E3 (without XhoI and BglII-site): no DNA: inoculation of an ONC </td>
</tr>
</tr>

Revision as of 18:52, 13 October 2014

Notebook / Locate GFP and the CBD

Here we list all the steps that were tested to modify the pORE E3 (AY562536.1) into a vector with BioBrick RFC[21]MCS and 2x35S promotor.

date

coworkers

lab

activity

short summary

25-Sept-2014 Lisa IPG colony-PCR colony-PCR with primer 1261 and 488: all 24 colonies negative or inconclusive/ no more time to do the insertion of rcf again
24-Sept-2014 Steffen, Lisa IPG triple digest/ oligo annealing vector: triple digest: gel extraction/ insert: oligo annealing/ phosphorylation/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells/ incubation over night (25 °C)/ everything performed after modified protocol
23-Sept-2014 Steffen IPG plasmidpreparation/ amplification of pORE_E3 plasmidpreparation of ONC from Katharina/ amplification
22-Sept-2014 Lisa, Katharina IPG insertion of RFC[21] colony-PCR: only negative controls/ consultation of TR: modification of the protocol
19-Sept-2014 Katharina IPG insertion of RFC[21] plasmid isolation from ONC/ Digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells/ incubation over night (25 °C)
18-Sept-2014 Katharina IPG insertion of RFC[21] digestion of pORE-E3 (without XhoI- and BglII-site): no DNA: inoculation of an ONC
17-Sept-2014 Katharina, Björn IPG insertion of RFC[21] colony-PCR with primer 1261 and 488: all 60 colonies negative: digestion probably went wrong/ isolation of plasmid of another ONC via handpreparation
16-Sept-2014 Katharina, Björn IPG insertion of RFC[21] plasmid isolation from ONC/ digestion of pORE-E3 (without XhoI and BglII-site) with MluI and BamHI/ annealing two primers (3 and 4) to build the rcf/ phosphorylation of primer construct/ dephosphorylation of digested vector/ ligation of vector and insert/ transformation of XL1-Blue Competent Cells
15-Sept-2014 Katharina, Björn IPG insertion of RFC[21] digestion of pORE-E3 (without XhoI and BglII-site): no DNA: inoculation of an ONC
27-Aug-2014 Melanie, Lisa IPG plasmidpreparation/ sequencing.v1 plasmidpreparation with 12 colonies/ double digestion (XhoI and NcoI): 7 might be without BglII AND XhoI: sequencing with primer ??? (IPG) positive/ pORE_E3 2x35S (without T4MPB) and without BglII- and XhoI-site
26-Aug-2014 Melanie IPG ONC of 13 colonies (12+1 pos. control) several colonies on each plate (including pos. control)/ pick of 3 to 4 per plate/ ONC
25-Aug-2014 Melanie, Lisa IPG ligation/ transformation of XL1-Blue Competent Cells via heat-shock/ selection on kanamycin
22-Aug-2014 Melanie IPG digest of pORE_E3 2x35S (without T4MBP and without BglII-site) with XhoI, proofreading PCR digestion of pORE_E3 2x35S (without T4MBP and without BglII-site) with XhoI for 1h 37 °C showed complete digestion/ proofreading-PCR to avoid A-Tailing (Phusion)
20-Aug-2014 Melanie IPG sequencing.v3 (new primer) sequencing with primer 1356: positive: BglII-site destroyed
19-Aug-2014 Melanie IPG sequencing.v2 (same primer) sequencing with primer 1261 (IPG) again stopped 10 bp before BglII-site: no definite result: again
15-Aug-2014 Lisa IPG plasmidpreparation/ sequencing.v1 plasmidpreparation with 10 colonies/ digestion with BglI (twice): poor results: 1 probe might be without BglII: sequencing with primer 1261 (IPG) of this probe stopped 10 bp before BglII-site: no definite result: again
13-Aug-2014 Melanie, Lisa IPG ONC of 10 colonies (9+1 pos. control) several colonies on each plate (including pos. control): pick of 3 per plate: ONC
12-Aug-2014 Melanie IPG transformation of E. coli with pORE_E3 2x35S (without T4MBP) ?without? BglII transformation via heat-shock/ selection on kanamycin
11-Aug-2014 Melanie, Lisa IPG digest of pORE_E3 2x35S (without T4MBP) with BglII/ proofreading PCR/ ligation digestion of pORE_E3 2x35S (without T4MPB) with BglII for 1h 37 °C: complete digestion/ proofreading-PCR to avoid A-Tailing (Phusion)/ ligation