<div class="row"><div class="col-xs-12"><button type="button" onclick="location.href='https://2016.igem.org/Team:Valencia_UPV/Protocols'">ALISIA PROTOCOLOS POR AQUÍ</button></div><div class="col-xs-6"><h3 style="color:green">18/05/2016</h3><p>Take glycerinated cultures of C58 <i>Agrobacterium</i> with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.</p></div><div class="col-xs-6"><h3 style="color:green">19/05/2016</h3><p>Refresh previously made culture by inoculating 10 μL in a new culture medium.</p></div></div>
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<div class="row"><div class="col-xs-6 col-xs-offset-3"><h3 style="color:green">20/05/2016</h3><p>Agroinfiltration in <i>Nicotiana benthamiana</i> of C58 with dsRED. <a href="" target="blank"></a></p><br><h3 style="color:green">06/06/2016</h3><ul><li>Take from the glycerinates of Goldenbraid Collection: </li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Plasmid</td><td>GB Code</td></tr><tr><td>pD6B3 α1</td><td>GB0015</td></tr><tr><td>pD6B3 α2</td><td>GB0017</td></tr><tr><td>pD6B3 Ω1</td><td>GB0019</td></tr><tr><td>pD6B3 Ω2</td><td>GB0021</td></tr><tr><td>pUPD2</td><td>GB0307</td></tr></tbody></table></div><ul><li>Prepare liquid culture (3 mL LB + 3 μL antibiotic) 1:1000. Incubate at 37°C overnight.</li></ul><ul><li>Experiment with snails:</li></ul><p>Let both <i>N. benthamiana</i> leafs with snails overnight at room temperature in separated boxes. We will observe if snails eat the leafs and if appears fluorescence.</p><br><h3 style="color:green">15/06/2016</h3><p>Experiment is over due to snails haven’t eaten leafs enough so we have not been able to see fluorescence.</p><br><h3 style="color:green">30/06/2016</h3><ul><li>Orange DNA Genome Extraction protocol <a href="" target="blank"></a></li></ul><ul><li>Take from the glycerinates of GoldenBraid Collection:</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Plasmid</td><td>GB Code</td></tr><tr><td>Promoter 35s:Cas9:nopaline synthase terminator (Tnos)</td><td>GB0639</td></tr><tr><td>Luciferase (Luc) in pUPD2</td><td>GB0096</td></tr><tr><td>Tnos in pUPD2</td><td>GB0037</td></tr></tbody></table></div><br><h3 style="color:green">01/07/2016</h3><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of: </li><ul class="ul_2"><li>Promoter 35s:Cas9 : Tnos</li></ul></ul><ul><li>Luciferase and nopaline synthase terminator cultures haven’t succeed. Repeat Luc and Tnos cultures.</li></ul><ul><li>Primers IG16JUN01 and IG16JUN02 have arrived.</li></ul><ul><li>Finish orange DNA Genome Extraction and check DNA concentration with NanoDrop. Concentration is very low so extraction will be done again.</li></ul><br><h3 style="color:green">02/07/2016</h3><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>Luc in pUPD2</li><li>Tnos in pUPD2</li></ul></ul><ul><li>Check orange DNA genome concentration with NanoDrop. </li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Sample</td><td>DNA concentration (ng / μL)</td></tr><tr><td>Clemenules1 </td><td>3153.8</td></tr><tr><td>Clemenules 2 </td><td>4527.9</td></tr></tbody></table></div><ul><li>Perform a PCR to bind linker with luciferase:</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume(μL)</td><td colspan="3" style="text-align:center">Program</td></tr><tr><td>LuciferasepUPD</td><td>1</td><td>Temperature</td><td colspan="2" style="text-align:center">Time </td></tr><tr><td>Buffer HF</td><td>10</td><td>98°C</td><td colspan="2" style="text-align:center">5 minutes </td></tr><tr><td>dNTPs</td><td>2</td><td>98°C</td><td style="text-align: center; vertical-align: middle;" rowspan="3">35x</td><td>30 seconds</td></tr><tr><td>IG16JUN01</td><td>2.5</td><td>70°C</td><td>30 seconds</td></tr><tr><td>IG16JUN02</td><td>2.5</td><td>72°C</td><td>1 minute 30 seconds</td></tr><tr><td>Taq phusion</td><td>0.5</td><td>72°C</td><td colspan="2" style="text-align:center">10 minutes </td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>31.5</td><td>16°C</td><td colspan="2" style="text-align:center">∞ </td></tr></tbody></table></div><br><h3 style="color:green">04/07/2016</h3><ul><li>Run electrophoresis gel of Clemenules DNA (agarose 1%). 45 mL agarose gel at 1% 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 100 V.</li></ul><ul><li>Rice DNA Genome Extraction Protocol <a href="" target="blank"></a></li></ul><ul><li>Run electrophoresis gel of Luciferase PCR product. 45 mL agarose gel at 1% 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 100 V.</li></ul><ul><li>Ligate Reaction</li></ul><ul><li>Transform <i>E. coli</i> DH5α with it. The method that is necessary to carry out this procedure is explained in protocols <a href="" target="blank"></a></li></ul><ul><li>Check DNA concentration with NanoDrop. </li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>SAMPLE</td><td>DNA Concentration(ng / μL)</td></tr><tr><td>Rice Gleva 1</td><td>22.8</td></tr><tr><td>Rice Gleva 2</td><td>17.3</td></tr></tbody></table></div><br><h3 style="color:green">05/07/2016</h3><ul><li>Run electrophoresis gel of Gleva rice DNA. We have checked that there isn’t DNA.</li></ul><ul><li>Repeat: Rice DNA Genome Extraction <a href="" target="blank"></a></li></ul><ul><li>Check DNA concentration with NanoDrop.</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>SAMPLE</td><td>DNA Concentration(ng / μL)</td></tr><tr><td>Rice Gleva 1</td><td>294.9</td></tr><tr><td>Rice Gleva 2</td><td>193.7</td></tr></tbody></table></div><ul><li>Run electrophoresis gel of Gleva rice DNA. It observed that genome extraction is correctly done.</li></ul><br><h3 style="color:green">06/07/2016</h3><p> Take glycerinated cultures from Goldenbraid Collection:</p><div class="table-wrapper"><table class="alt"><tbody><tr><td>GB part</td><td>Plasmid</td><td>Antibiotic</td><td>Number GB</td></tr><tr><td>psgRNA</td><td>pUPD</td><td>Ampicillin</td><td>0645</td></tr><tr><td>U6-26</td><td>pUPD</td><td>Ampicillin</td><td>1001</td></tr></tbody></table></div><br><h3 style="color:green">07/07/2016</h3><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>psgRNA in pUPD2</li><li>U6-26 in pUPD2</li></ul></ul><ul><li>Primers IG16JUL01, IG16JUL02, IG16JUL03, IG16JUL04, IG16JUL05, IG16JUL06, IG16JUL07 and IG16JUL08 arrived.</li></ul><ul><li>gBlocks of - promoter 35s:5’ region - have arrived.</li></ul><ul><li>We perform a PCR of orange and rice Genome Extraction following the protocol <a href="" target="blank"></a></li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Sample</td><td>Initial concentration(ng/μL)</td><td>Final concentration(ng/μL)</td><td>Initial volume(μL)</td><td>Final volume (μL)</td></tr><tr><td>Clemenules 1</td><td>3153.8</td><td>150</td><td>4.756</td><td>100</td></tr><tr><td>Clemenules 2</td><td>4527.9</td><td>150</td><td>3.31</td><td>100</td></tr><tr><td>Gleva 1</td><td>294.9</td><td>150</td><td>50.8647</td><td>100</td></tr><tr><td>Gleva 2</td><td>193.7</td><td>150</td><td>77.44</td><td>100</td></tr></tbody></table></div><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume(μL)</td><td colspan="3" style="text-align:center">Program</td></tr><tr><td> Clemenules DNA 1</td><td>1</td><td>Temperature</td><td colspan="2" style="text-align:center">Time </td></tr><tr><td>Buffer HF</td><td>10</td><td>98°C</td><td colspan="2" style="text-align:center">5 minutes </td></tr><tr><td>dNTPs</td><td>2</td><td>98°C</td><td style="text-align: center; vertical-align: middle;" rowspan="3">35x</td><td>30 seconds</td></tr><tr><td>IG16JUL01 (TFL_For)</td><td>2.5</td><td>64°C</td><td>30 seconds</td></tr><tr><td>IG16JUL02 (TFL_Rev)</td><td>2.5</td><td>72°C</td><td>30 seconds</td></tr><tr><td>Taq phusion</td><td>0.5</td><td>72°C</td><td colspan="2" style="text-align:center">10 minutes </td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>31.5</td><td>16°C</td><td colspan="2" style="text-align:center">∞</td></tr></tbody></table></div><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume(μL)</td><td colspan="3" style="text-align:center">Program</td></tr><tr><td> Gleva DNA</td><td>1</td><td>Temperature</td><td colspan="2" style="text-align:center">Time </td></tr><tr><td>Buffer HF</td><td>10</td><td>98°C</td><td colspan="2" style="text-align:center">5 minutes </td></tr><tr><td>dNTPs</td><td>2</td><td>98°C</td><td style="text-align: center; vertical-align: middle;" rowspan="3">35x</td><td>30 seconds</td></tr><tr><td>IG16JUL03 (Ga20_for)</td><td>2.5</td><td>72°C</td><td>30 seconds</td></tr><tr><td>IG16JUL02 (Ga20_rev)</td><td>2.5</td><td>72°C</td><td>30 seconds</td></tr><tr><td>Taq phusion</td><td>0.5</td><td>72°C</td><td colspan="2" style="text-align:center">10 minutes </td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>31.5</td><td>16°C</td><td colspan="2" style="text-align:center">∞ </td></tr></tbody></table></div><ul><li>Ligate reaction of promoter 35s:5’ region in pUPD2. Following ligation protocol <a href="" target="blank"></a>, BsmbI enzyme is used in this reaction.</li></ul><br><h3 style="color:green">08/07/2016</h3><ul><li>Run electrophoresis gel of Clemenules and Gleva PCR products. 45 mL agarose gel at 1 % 0.45 g of agarose with 45 mL of TAE 1X. Voltage used is 120 V.</li></ul><ul><li>Transform <i>E. coli</i> with the next devise: promoter 35s:5’ region (electroporation 2.5KV). Plating it and incubate overnight at 37°C.</li></ul><ul><li>Take glycerinated culture for Georgia collaboration. The devise is promoter 35s:GFP:Tnos (α1 and kanamycin)</li></ul><br><h3 style="color:green">09/07/2016</h3><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>promoter 35s:GFP:Tnos</li></ul></ul><ul><li>No colonies have grown in the devise promoter 35s:5’ region petri dishes. Repeat transformation procedure, plating again and incubate overnight at 37°C.</li></ul><br><h3 style="color:green">11/07/2016</h3><ul><li>Pick a single E. coli DH5α (promoter 35s:5’ region in pUPD2) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it overnight at 37°C with shaking.</li></ul><ul><li>Check Georgia miniprep concentration with NanoDrop (promoter 35s:GFP : Tnos)</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Sample</td><td>DNA Concentration(ng / μL)</td><td>DNA Concentration(ng)</td></tr><tr><td>1</td><td>105.2</td><td>5035.2</td></tr><tr><td>2</td><td>104.6</td><td>5035.2</td></tr></tbody></table></div><ul><li>Targets ligations in pUPD2 (Orange Clemenules and Rice Gleva). Following ligation protocol <a href="" target="blank"></a>, BsmbI enzyme is used in this reaction.</li></ul><br><h3 style="color:green">12/07/2016</h3><ul><li>Pick a single E. coli DH5α (target Gleva in pUPD2 and target Clemenules in pUPD2) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it 16 hours at 37°C.</li></ul><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of: </li><ul class="ul_2"><li>Promoter 35s:5’region in pUPD2</li></ul></ul><ul><li>Digestion of minipreps with NotI. Incubate 1 hour at 37°C</li></ul><ul><li>Run electrophoresis gel of the following devise: promoter 35s:5’ region in pUPD2. We remain the samples 1 and 3.</li></ul><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of: </li><ul class="ul_2"><li>Rice Gleva target in pUPD2</li><li>Orange Clemenules target in pUPD2</li></ul></ul><ul><li>Digestion of minipreps with NotI. Incubate 1 hour at 37°C.</li></ul><ul><li>Run electrophoresis gel of the same devise:</li><ul class="ul_2"><li>Rice Gleva target in pUPD2</li><li>Orange Clemenules target in pUPD2</li></ul></ul><ul><li>Ligation using Golden Braid assembly of the next devise:</li><ul class="ul_2"><li>Promoter 35s:5’ region:Target:Luc:Tnos in α1 plasmid.</li></ul></ul><br><h3 style="color:green">13/07/2016</h3><ul><li><i>E. coli</i> Transformation with the devise:</li><ul class="ul_2"><li>Promoter 35s:5’ region:Target:Luc:Tnos in α1 plasmid.</li></ul></ul><ul><li>E. coli plating in plates with Kanamycin (antibiotic). Incubate overnight at 37°C</li></ul><br><h3 style="color:green">14/07/2016</h3><ul><li>Pick a single E. coli DH5α (promoter 35s:5’ region) colony from the plate that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of chloramphenicol in a 50 ml tube with the colony and incubate it 16 hours at 37°C.</li></ul><ul><li>Primers IG16JUL09, IG16JUL10, IG16JUL11, IG16JUL12, IG16JUL13, IG16JUL14, IG16JUL15 and IG16JUL16 arrived.</li></ul><ul><li>Ligation using Golden Braid assembly of the next devises:</li><ul class="ul_2"><li>promoter 35s:5’ region:Clemenules target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:Gleva target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:Clemenules target consensus:Luc:Tnos</li><li>promoter 35s:5’ region:Gleva target consensus:Luc:Tnos</li><li>promoter U6-26:sgRNA Clemenules: psgRNA (scaffold)</li><li>promoter U6-26:sgRNA Gleva: psgRNA (scaffold)</li></ul></ul><ul><li>Step 1: Annealing of oligonucleotides. Received primers are at 1uM. It is necessary taking to 10 uM.</li></ul><ul><li>Mix in an Eppendorf:</li><li>18 μL of H<sub>2</sub>O milli-Q</li><li>1 μL forward primer</li><li>1 μL reverse primer</li></ul><ul><li>Step 2: Ligation reaction</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td></td><td>Reagent</td><td>Volume (μL)</td></tr><tr><td></td><td>Target control positive / Target consensus</td><td>1 </td></tr><tr><td></td><td>promoter 35s:5’ region</td><td>1</td></tr><tr><td></td><td>Luciferase</td><td>1</td></tr><tr><td></td><td>Tnos</td><td>1</td></tr><tr><td></td><td>α1 plasmid</td><td>1</td></tr><tr><td></td><td>BSA10X</td><td>1.2</td></tr><tr><td></td><td>Ligase Buffer</td><td>1.2</td></tr><tr><td></td><td>BsaI</td><td>1</td></tr><tr><td></td><td>T4 ligase</td><td>1</td></tr><tr><td></td><td>H<sub>2</sub>O milli-Q</td><td>2.6</td></tr></tbody></table></div><p> </p><p> </p><div class="table-wrapper"><table class="alt"><tbody><tr><td></td><td>Reagent</td><td>Volume (μL)</td></tr><tr><td></td><td>sgRNA Clemenules / sgRNA Gleva</td><td>1</td></tr><tr><td></td><td>promoter U6 -26</td><td>1</td></tr><tr><td></td><td>psgRNA (scaffold)</td><td>1</td></tr><tr><td></td><td>α1 plasmid</td><td>1</td></tr><tr><td></td><td>BSA10X</td><td>1.2</td></tr><tr><td></td><td>Ligase Buffer</td><td>1.2</td></tr><tr><td></td><td>BsaI</td><td>1</td></tr><tr><td></td><td>T4 ligase</td><td>1</td></tr><tr><td></td><td>H<sub>2</sub>O milli-Q</td><td>3.6</td></tr></tbody></table></div><p> </p><ul><li><i>E. coli</i> Transformation with the devises previously explained.</li></ul><ul><li>E. coli plating in 6 plates (6 ligation reactions) with Kanamycin (antibiotic). Incubate overnight at 37°C.</li></ul><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of: </li><ul class="ul_2"><li>Promoter 35s:5’ region : CL target : Luc : Tnos (3α1)</li><li>Promoter 35s:5’ region : A target : Luc : Tnos (3α1)</li></ul></ul><ul><li>Digestion of minipreps with EcoRI. Incubate 1 hour at 37°C</li></ul><br><h3 style="color:green">15/07/2016</h3><ul><li>Ligation using Golden Braid assembly of the next devises: </li><ul class="ul_2"><li>Promoter 35s:Cas9:Tnos – promoter 35s:5’ region:TFL Clemenules target:Luc:Tnos</li><li>Promoter 35s:Cas9:Tnos – promoter 35s:5’ region:Ga20ox Rice target:Luc:Tnos</li></ul></ul><ul><li>E. coli Transformation with the devises previously explained.</li></ul><ul><li>Run an electrophoresis gel of the products from the digestion of minipreps. The devises are:</li><ul class="ul_2"><li>Promoter 35s:5’ region:TFL Clemenules target:Luc:Tnos (3α1)</li><li>Promoter 35s:5’ region :Ga20ox Rice target:Luc:Tnos (3α1)</li></ul></ul><ul><li>Sequencing the following products:</li><ul class="ul_2"><li>Promotor 35s:5’ region in pUPD2 → correct</li></ul></ul><br><h3 style="color:green">16/07/2016</h3><ul><li>Transformations in <i>E. coli</i> DH5α with:</li><ul class="ul_2"><li>Promoter 35s:5’ region:TFL Clemenules target:Luc:Tnos (3α1)</li><li>Promoter 35s:5’ region:Ga20ox Rice target:Luc:Tnos (3α1)</li></ul></ul><ul><li>Plating the last devises in 2 plates with <i>Agrobacterium</i> C58. Incubate 2 days at 28°C.</li></ul><ul><li>Minipreps (2 samples for each devise) with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>Promoter 35s:5’ region:Clemenules target control positive:Luc:Tnos</li><li>Promoter 35s:5’ region:Gleva target control positive:Luc:Tnos</li><li>Promoter 35s:5’ region:Clemenules target consensus:Luc:Tnos</li><li>Promoter 35s:5’ region:Gleva target consensus:Luc:Tnos</li><li>Promoter U6-26:sgRNA Clemenules:psgRNA (scaffold)</li><li>Promoter U6-26:sgRNA Gleva:psgRNA (scaffold)</li></ul></ul><ul><li>Ligation using Golden Braid assembly of the next devises: </li><ul class="ul_2"><li>Promotor 35s:Cas9:Tnos – U6:TFL Clemenules sgRNA:psgRNA (scaffold) (Ω1)</li><li>Promotor 35s:Cas9:Tnos – U6: Ga20ox Rice sgRNA:psgRNA (scaffold) (Ω1)</li></ul></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume (μL)</td></tr><tr><td>Promotor 35s:Cas9 : Tnos</td><td>1</td></tr><tr><td>U6-26:TFL Clemenules sgRNA:psgRNA / U6-26:Ga20ox rice sgRNA:psgRNA</td><td>1</td></tr><tr><td>3Ω1</td><td>1</td></tr><tr><td>BSA10X</td><td>1.2</td></tr><tr><td>Ligase Buffer</td><td>1.2</td></tr><tr><td>BsmbI</td><td>1</td></tr><tr><td>T4 ligase</td><td>1</td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>4.6</td></tr></tbody></table></div><ul><li>Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of twelve minipreps. It has been followed the Miniprep digestion protocol <a href="" target="blank"></a>.</li></ul><ul><li>Run electrophoresis gel of the digestion products.</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Lanes</td><td>Samples</td><td>Verification</td></tr><tr><td>1</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>2</td><td>gRNA Ga20ox 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>3</td><td>gRNA Ga20ox 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>4</td><td>Ga20ox consensus 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>5</td><td>Ga20ox consensus 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>6</td><td>Ga20ox knock-out 1</td><td><img src="https://static.igem.org/mediawiki/2016/7/7a/T--Valencia_UPV--cross.png" class="check_img"></td></tr><tr><td>7</td><td>Ga20ox knock-out 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>8</td><td>TFL consensus 1</td><td><img src="https://static.igem.org/mediawiki/2016/7/7a/T--Valencia_UPV--cross.png" class="check_img"></td></tr><tr><td>9</td><td>TFL consensus 2</td><td><img src="https://static.igem.org/mediawiki/2016/7/7a/T--Valencia_UPV--cross.png" class="check_img"></td></tr><tr><td>10</td><td>TFL knock-out 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>11</td><td>TFL knock-out 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>12</td><td>TFL gRNA 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>13</td><td>TFL gRNA 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>14</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr></tbody></table></div><ul><li>Pick a single E. coli DH5α colony from the plates that have been incubated overnight. The devises are:</li><ul class="ul_2"><li>Promoter 35s:TFL Knock-out:Luc:Tnos (4 samples)</li><li>Promoter U6-26:Ga20ox sgRNA:psgRNA (2 samples)</li></ul></ul><ul><li>Inoculate a starter culture of 4 ml of LB medium with 4 μL of kanamycin in a 50 ml tube with the colony and incubate it 16 hours at 37°C.</li></ul><br><h3 style="color:green">17/07/2016</h3><ul><li>Transformation in DH5α <i>E. coli</i> with:</li><ul class="ul_2"><li>Promoter 35s:Cas9:Tnos – U6:TFL Clemenules sgRNA:psgRNA (scaffold) (Ω1)</li><li>Promoter 35s:Cas9:Tnos – U6:Ga20ox sgRNA:psgRNA (scaffold) (Ω1)</li></ul></ul><ul><li>Plating <i>E. coli</i> transformations in plates with LB + agar + IPTG + XGal and incubate it overnight at 37°C.</li></ul><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of: </li><ul class="ul_2"><li>Promoter U6-26:Ga20ox sgRNA:psgRNA </li><li>Promoter 35s:5’ region:TFL Knock-out:Luc:Tnos (3α1)</li></ul></ul><ul><li>Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of six minipreps. It has been followed the Miniprep digestion protocol <a href="" target="blank"></a>.</li></ul><ul><li>Run an electrophoresis gel of the digestion products.</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Lanes</td><td>Samples</td><td>Verification</td></tr><tr><td>1</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>2</td><td>gRNA Ga20ox 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>3</td><td>gRNA Ga20ox 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>4</td><td>gRNA Ga20ox 3</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>5</td><td>gRNA Ga20ox 4</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>6</td><td>TFL knock-out 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>7</td><td>TFL knock-out 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>8</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr></tbody></table></div><p>However, despite the fact that electrophoresis gel have correctly run, we have decided to repeat the ligation reactions. We have not get the expected results for a gRNA.</p><ul><li>Ligation using Golden Braid assembly of the next devises:</li><ul class="ul_2"><li>Promoter 35s:5’ region:TFL Clemenules target control positive:Luc:Tnos</li><li>Promoter 35s:5’ region:Ga20ox Gleva target control positive:Luc:Tnos</li><li>Promoter 35s:5’ region:TFL Clemenules target consensus:Luc:Tnos</li><li>Promoter 35s:5’ region:Ga20ox Gleva target consensus:Luc:Tnos</li><li>Promoter U6-26:sgRNA Clemenules:psgRNA (scaffold)</li><li>Promoter U6-26:sgRNA Gleva:psgRNA (scaffold)</li></ul></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume(μL)</td><td>Reagent</td><td>Volume(μL)</td></tr><tr><td>TFL/Ga20ox gRNA</td><td>1</td><td>promoter 35s:5’region</td><td>1</td></tr><tr><td>U6-26</td><td>1</td><td>TFL/Ga20ox consensus TFL/Ga20ox knock-out</td><td>1</td></tr><tr><td>psgRNA</td><td>1</td><td>luciferase</td><td>1</td></tr><tr><td>3α1</td><td>1</td><td>Tnos</td><td>1</td></tr><tr><td>BSA10X</td><td>1.2</td><td>3α1</td><td>1</td></tr><tr><td>Ligase Buffer</td><td>1.2</td><td>BSA10X</td><td>1.2</td></tr><tr><td>BsaI</td><td>1</td><td>Ligase Buffer</td><td>1.2</td></tr><tr><td>T4 ligase</td><td>1</td><td>BsmbI</td><td>1</td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>3.6</td><td>T4 ligase</td><td>1</td></tr><tr><td></td><td></td><td>H<sub>2</sub>O milli-Q</td><td>2.6</td></tr></tbody></table></div><br><h3 style="color:green">18/07/2016</h3><ul><li>Transformation in DH5α <i>E. coli</i> with ligation products (consensus targets and knock-out targets of TFL and Ga20ox as well as their gRNAs)</li></ul><ul><li>Plating <i>E. coli</i> transformations in plates with LB + agar + IPTG + XGal and incubate it overnight at 37°C.</li></ul><ul><li>Pick a single <i>Agrobacterium</i> C58 colony from the plates that have been incubating since 16/06/2016. The devises are:</li><ul class="ul_2"><li>Promoter 35s:5’ region:TFL Clemenules target:Luc:Tnos (3α1)</li><li>Promoter 35s:5’ region:Ga20ox Rice target:Luc:Tnos (3α1)</li></ul></ul><ul><li>Incubate it 48 hours at 28°C.</li></ul><br><h3 style="color:green">19/07/2016</h3><ul><li>Pick transformed <i>E. coli</i> colony from the incubated plates. The devises are:</li><ul class="ul_2"><li>promoter 35s:5’ region:TFL Clemenules target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:TFL Clemenules target consensus:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target consensus:Luc:Tnos</li><li>promoter U6-26: sgRNA Clemenules:psgRNA (scaffold)</li><li>promoter U6-26: sgRNA Gleva:psgRNA (scaffold)</li></ul></ul><ul><li>Incubate it overnight at 37°C.</li></ul><br><h3 style="color:green">20/07/2016</h3><p> </p><ul><li>Miniprep with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>promoter 35s:5’ region:TFL Clemenules target knock-out:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target control knock-out:Luc:Tnos</li><li>promoter 35s:5’ region:TFL Clemenules target consensus:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target consensus:Luc:Tnos</li><li>promoter U6-26:sgRNA TFL Clemenules:psgRNA (scaffold)</li><li>promoter U6-26:sgRNA Ga20ox Gleva:psgRNA (scaffold)</li></ul></ul><ul><li>Digestion of the minipreps with EcoRI which have been done before. Incubate 1 hour at 37°C. There is a total of six minipreps. It has been followed the Miniprep digestion protocol <a href="" target="blank"></a>.</li></ul><ul><li>Run an electrophoresis gel of the digestion products. We will keep the minipreps with “1”.</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Lanes</td><td>Samples</td><td>Verification</td></tr><tr><td>1</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>2</td><td>gRNA TFL 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>3</td><td>gRNA TFL 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>4</td><td>TFL consensus 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>5</td><td>TFL consensus 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>6</td><td>TFL knock-out 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>7</td><td>TFL knock-out 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>8</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>9</td><td>gRNA Ga20ox 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>10</td><td>gRNA Ga20ox 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>11</td><td>Ga20ox consensus 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>12</td><td>Ga20ox consensus 2</td><td><img src="https://static.igem.org/mediawiki/2016/7/7a/T--Valencia_UPV--cross.png" class="check_img"></td></tr><tr><td>13</td><td>Ga20ox knock-out 1</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>14</td><td>Ga20ox knock-out 2</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>15</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr></tbody></table></div><ul><li>Ligation using Golden Braid assembly of the next devises. Is used the restriction enzyme BsmbI.</li><ul class="ul_2"><li>promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA</li><li>Promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA</li></ul></ul><br><h3 style="color:green">21/07/2016</h3><p> </p><ul><li>Transformations in <i>E. coli</i> DH5α with:</li><ul class="ul_2"><li>promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA</li><li>promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA</li></ul></ul><p>Incubate 2 hours at 37°C.</p><ul><li>Plating <i>E. coli</i> transformation explained before and incubate it at 37°C overnight.</li></ul><ul><li><i>Agrobacterium</i> C58 transformation with:</li><ul class="ul_2"><li>promoter 35s:5’ region:TFL Clemenules target knock-out:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target control knock-out:Luc:Tnos</li><li>promoter 35s:5’ region:TFL Clemenules target consensus:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target consensus:Luc:Tnos</li></ul></ul><p>Incubate 48 hours at 28°C.</p><p> </p><br><h3 style="color:green">22/07/2016</h3><p> </p><ul><li>Sequencing reaction:</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Reagent</td><td>Volume (μL)</td></tr><tr><td>Primer in order to sequence</td><td>3</td></tr><tr><td>Miniprep reaction</td><td>5</td></tr><tr><td>H<sub>2</sub>O milli-Q</td><td>6</td></tr></tbody></table></div><div class="table-wrapper"><table class="alt"><tbody><tr><td>Sequence</td><td>Order</td></tr><tr><td>TFL gRNA</td><td>210.13.201</td></tr><tr><td>Ga20 gRNA</td><td>210.13.202</td></tr></tbody></table></div><ul><li>Ordered the necessary primers to sequence: TFL consensus, TFL knockout, Ga20ox consensus and Ga20ox knockout.</li></ul><ul><li><i>E. coli</i> transformations with:</li><ul class="ul_2"><li>Promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA: psgRNA</li></ul></ul><ul><li>Plating the last devise in plates with <i>Agrobacterium</i> C58. Plates contain spec + IPTG + X-Gal. Incubate 2 days at 28°C.</li></ul><ul><li>Pick a single <i>E. coli</i> DH5α (promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA and promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA) colony from the plates that has been incubated overnight. Inoculate a starter culture of 4 ml of LB medium with 4 μL of spectinomycin in a 50 ml tube with the colony and incubate it overnight at 37°C with shaking.</li></ul><br><h3 style="color:green">23/07/2016</h3><p> </p><ul><li>Minipreps (4 samples for each devise) with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA</li><li>promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA</li></ul></ul><ul><li>Digestion of minipreps with BamHI following digestion protocol <a href="" target="blank"></a>. Incubate 1 hour at 37°C.</li></ul><ul><li>Run an electrophoresis gel of the digestion products. We will keep the minipreps with the sample number 4 for TFL sgRNA and the sample number 2 for Ga20ox sgRNA.</li></ul><ul><li>Pick a single <i>Agrobacterium</i> C58 (promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA and promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA ) colony from the plates that has been incubated overnight. Inoculate a starter culture of 5 ml of LB medium with 5 μL of spectinomycin and kanamycin in a falcon tube with the colony and incubate it overnight at 28°C with shaking.</li></ul><ul><li><i>Agrobacterium</i> C58 transformations with:</li><ul class="ul_2"><li>promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA</li><li>promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA</li></ul></ul><br><h3 style="color:green">24/07/2016</h3><p> </p><ul><li>Store the next cultures at -80°C:</li><ul class="ul_2"><li>promoter 35s:5’ region in pUPD2 (DH5α) number 1</li><li>Linker: luciferase in pUPD2 (DH5α) number 2</li></ul></ul><br><h3 style="color:green">25/07/2016</h3><ul><li>Pick a single <i>Agrobacterium</i> C58 (promoter 35s:Cas 9:Tnos – U6-26:TFL sgRNA:psgRNA in 3Ω1 and promoter 35s:Cas 9:Tnos – U6-26:Ga20ox sgRNA:psgRNA in 3Ω1 ) colony from the plates that has been incubated overnight. Inoculate a starter culture of 5 ml of LB medium with 5 μL of spectinomycin and kanamycin in a falcon tube with the colony and incubate it overnight at 28°C with shaking.</li></ul><ul><li>Incubate it 48 hours at 28°C</li></ul><ul><li>Minipreps of <i>Agrobacterium</i> with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>promoter 35s:5’ region:TFL Clemenules target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target control positive:Luc:Tnos</li><li>promoter 35s:5’ region:TFL Clemenules target consensus:Luc:Tnos</li><li>promoter 35s:5’ region:Ga20ox Gleva target consensus:Luc:Tnos</li></ul></ul><ul><li>Digestion of minipreps with the restriction enzyme EcoRI. Incubate 1 hour at 37°C.</li></ul><ul><li>Run an electrophoresis gel of the digestion products.</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Lanes</td><td>Samples</td><td>Verification</td></tr><tr><td>1</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>2</td><td>Target Ga20ox consensus</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>3</td><td>Target Ga20ox Knock-out</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>4</td><td>Target TFL consensus</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>5</td><td>Target TFL knock-out</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>6</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr></tbody></table></div><br><h3 style="color:green">26/07/2016</h3><ul><li>Minipreps with E.Z.N.A. ® Plasmid Mini Kit I, Q(capless) Spin of:</li><ul class="ul_2"><li>promoter 35s:5’ region:TFL Clemenules target:Luc:Tnos in 3α1 plasmid from C58 <i>Agrobacterium</i></li><li>promoter 35s:5’ region:Ga20ox Gleva target:Luc:Tnos in 3α1 plasmid from C58 <i>Agrobacterium</i></li></ul></ul><ul><li>Digestion of minipreps with the restriction enzyme EcoRI. Incubate 1 hour at 37°C.</li></ul><ul><li>Run an electrophoresis gel of the digestion products:</li></ul><div class="table-wrapper"><table class="alt"><tbody><tr><td>Lanes</td><td>Samples</td><td>Verification</td></tr><tr><td>1</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>2</td><td>promoter 35s:5’ region:Target Ga20ox Rice:Luc:Tnos </td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>3</td><td>promoter 35s:5’ region:Target TFL Clemunules:Luc:Tnos </td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr><tr><td>6</td><td>1 Kb molecular weight marker</td><td><img src="https://static.igem.org/mediawiki/2016/b/b7/T--Valencia_UPV--check.png" class="check_img"></td></tr></tbody></table></div><p> </p><p> </p><p> </p><p> </p><p></p></div></div>
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May 18, 2016
Take glycerinated cultures of C58 Agrobacterium with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.
May 19, 2016
Agroinfiltration in Nicotiana benthamiana of C58 with dsRED.
May 18, 2016
Take glycerinated cultures of C58 Agrobacterium with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.
May 19, 2016
Agroinfiltration in Nicotiana benthamiana of C58 with dsRED.
May 18, 2016
Take glycerinated cultures of C58 Agrobacterium with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.
May 19, 2016
Agroinfiltration in Nicotiana benthamiana of C58 with dsRED.
May 18, 2016
Take glycerinated cultures of C58 Agrobacterium with dsRED from GoldenBraid Collection. Prepare broth culture (5 mL LB + 5 μL kanamycin + 5 μL Rifampin) 1:1000 and incubate overnight at 28°C.
May 19, 2016
Agroinfiltration in Nicotiana benthamiana of C58 with dsRED.
