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− | <h3> | + | <h3>Alternative Roots</h3> |
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− | + | Protocols <br> | |
− | + | <br> | |
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− | + | Overview | |
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− | <section id=' | + | <section id='protocol' class="s-services"> |
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<div class="col-full"> | <div class="col-full"> | ||
− | <h3 class="subhead"> | + | <h3 class="subhead">EXPERIMENTS</h3> |
− | <h1 class="display-2"> | + | <h1 class="display-2">PROTOCOLS</h1> |
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− | <div class="row services-list | + | <div style="padding-bottom: 20px;" class="row services-list block-1-2 block-tab-full" data-aos="fade-up"> |
− | < | + | <table id="protocols"> |
− | + | <thead> | |
− | + | <tr> | |
− | + | <th>Protocol</th> | |
− | + | <th>Author</th> | |
− | + | <th>Category</th> | |
− | + | <th>PDF File</th> | |
− | + | </tr> | |
− | + | </thead> | |
− | + | <tbody> | |
− | + | <tr> | |
− | + | <td>Glycerol Stock Preserves</td> | |
− | + | <td>Connor Trotter</td> | |
− | + | <td>General</td> | |
+ | <td><a href="https://static.igem.org/mediawiki/2018/5/5a/T--Newcastle--GlycerolStock1.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Bacterial Isolation from Freeze-Dried Pellet</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>General</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/7/72/T--Newcastle--BacIsolation1.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Cell Counting</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/8/89/T--Newcastle--Haemocytometer1.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Seeding Cells in ibidi µ-Slide III 3-in-1 Chemotaxis Microscopy Slide</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/7/7d/T--Newcastle--ibidiprotocol.pdf" style="color:green">View<a/></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Minimal A Salt Agar Chemotaxis Assay</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/7/7f/T--Newcastle--MinAgar.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | |||
+ | <tr> | ||
+ | <td>0.75 % Agar Chemotaxis Assay</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/4/47/T--Newcastle--0.5ProtocolRedone.pdf" style="color:green">View<a/></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>0.50 % Agar Chemotaxis Assay</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/2/2a/T--Newcastle--0.5%25ProtocolRedoneTrue.pdf" style="color:green">View<a/></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Growth Curve in Liquid Culture</td> | ||
+ | <td>Sadiya Quazi</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/6/6a/T--Newcastle--GCIL.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <tr> | ||
+ | <td>Quantitative Capillary Assay</td> | ||
+ | <td>Connor Trotter</td> | ||
+ | <td>Chemotaxis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/a/a1/T--Newcastle--CapillaryAssayChemo.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
− | + | <tr> | |
− | + | <td>Naringenin Kill Curve in Liquid Culture</td> | |
− | + | <td>Sadiya Quazi</td> | |
− | + | <td>Chemotaxis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/7/76/T--Newcastle--NarKillCurves.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Planting Seeds in Agar-Filled Microcentrifuge Tubes</td> | |
− | + | <td>Lewis Tomlinson</td> | |
− | + | <td>Root Colonisation</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/e/e3/T--Newcastle--MCPlant.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Preparation and Staining of Microscopy Samples</td> | |
− | + | <td>Lewis Tomlinson</td> | |
− | + | <td>Root Colonisation</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/b/bd/T--Newcastle--MScopy.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Planting Seeds in Agar-Filled Pipette-Tip Racks</td> | |
− | + | <td>Lewis Tomlinson</td> | |
− | + | <td>Root Colonisation</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/7/7d/T--Newcastle--RCK.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Re-isolating Endophytes</td> | |
− | + | <td>Lewis Tomlinson</td> | |
− | + | <td>Root Colonisation</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/e/ef/T--Newcastle--RIso.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Electroporation of <I>Pseudomonas</I> sp.</td> | |
− | + | <td>Frank Eardley</td> | |
− | + | <td>Endophytic Chassis Development</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/b/bc/T--NEWCASTLE--Electroporation.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>MIC Opentrons Code (2 Plates)</td> | |
− | + | <td>Frank Eardley</td> | |
− | + | <td>Endophytic Chassis Development</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/a/af/T--Newcastle--KillCurveCodes.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>MIC Protocol</td> | |
− | + | <td>Frank Eardley</td> | |
− | + | <td>Endophytic Chassis Development</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/3/39/T--Newcastle--MICProtocol.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>MIC Plate Layout</td> | |
− | + | <td>Frank Eardley</td> | |
− | + | <td>Endophytic Chassis Development</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/b/bb/T--Newcastle--MICPlateLayout.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>2-Part Gibson Assembly</td> | |
− | + | <td>Frank Eardley</td> | |
− | + | <td>Endophytic Chassis Development</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/7/78/T--Newcastle--2PartGibson.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Amplification of gBlocks and Gradient PCR</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/8/87/T--Newcastle--GBAmp.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Colony PCR of Transformed DH5α Cells</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/a/a9/T--Newcastle--PCTransform.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>DpnI Digestion and Purification</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/b/b0/T--Newcastle--DPN1Diges.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Gel Extraction and Purification of the gBlocks</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/c/cc/T--Newcastle--GBlockGel.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Gibson Assembly of gBlocks and pSB1C3 Backbone</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/1/15/T--Newcastle--Gib.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Making Chemically Competent Cells</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/a/a6/T--Newcastle--CCell.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Miniprep of Transformed Colonies</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/0/02/T--Newcastle--MinPre.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Amplification, Purification and Quantification of the pSB1C3 Backbone by PCR</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/5/5f/T--Newcastle--PCReaction.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Quantifying DNA Concentration</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/0/03/T--Newcastle--QuantifyingDNA.pdf" style="color:green">View</a></td> | |
− | + | </tr> | |
− | + | <tr> | |
− | + | <td>Resuspending gBlocks and Primers</td> | |
− | + | <td>Heather Bottomley</td> | |
− | + | <td>Naringenin Operon Biosynthesis</td> | |
− | + | <td><a href="https://static.igem.org/mediawiki/2018/a/a0/T--Newcastle--GBlockFragmnt.pdf" style="color:green">View</a></td> | |
+ | </tr> | ||
+ | <tr> | ||
+ | <td>SOC Media Preparation</td> | ||
+ | <td>Heather Bottomley</td> | ||
+ | <td>Naringenin Operon Biosynthesis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/4/4e/T--Newcastle--SOC1.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Transformation of the Gibson assembly product into pSB1C3</td> | ||
+ | <td>Heather Bottomley</td> | ||
+ | <td>Naringenin Operon Biosynthesis</td> | ||
+ | <td><a href="https://static.igem.org/mediawiki/2018/1/15/T--Newcastle--GBTransform.pdf" style="color:green">View</a></td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
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+ | |||
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+ | <div class="row section-header has-bottom-sep" data-aos="fade-up"> | ||
+ | <div class="col-full"> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | <br> | ||
+ | <h3 class="subhead"></h3> | ||
+ | <h1 class="display-2">References & Attributions</h1> | ||
+ | </div> | ||
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+ | </div> | ||
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+ | <button class="collapsible">Click for References</button> | ||
+ | <div class="content"> | ||
+ | <div class="row about-desc" data-aos="fade-up"> | ||
+ | <div class="col-full"> | ||
+ | |||
+ | <p class="about-para"><font size="2"><strong>Attributions: Connor Trotter, Sadiya Quazi, Lewis Tomlinson, Frank Eardley, Heather Bottomley | ||
+ | </strong><font></p> | ||
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{{Newcastle/footer}} | {{Newcastle/footer}} |
Latest revision as of 00:50, 18 October 2018
Alternative Roots
Protocols
EXPERIMENTS
PROTOCOLS
Protocol | Author | Category | PDF File |
---|---|---|---|
Glycerol Stock Preserves | Connor Trotter | General | View |
Bacterial Isolation from Freeze-Dried Pellet | Connor Trotter | General | View |
Cell Counting | Connor Trotter | Chemotaxis | View |
Seeding Cells in ibidi µ-Slide III 3-in-1 Chemotaxis Microscopy Slide | Connor Trotter | Chemotaxis | View |
Minimal A Salt Agar Chemotaxis Assay | Connor Trotter | Chemotaxis | View |
0.75 % Agar Chemotaxis Assay | Connor Trotter | Chemotaxis | View |
0.50 % Agar Chemotaxis Assay | Connor Trotter | Chemotaxis | View |
Growth Curve in Liquid Culture | Sadiya Quazi | Chemotaxis | View |
Quantitative Capillary Assay | Connor Trotter | Chemotaxis | View |
Naringenin Kill Curve in Liquid Culture | Sadiya Quazi | Chemotaxis | View |
Planting Seeds in Agar-Filled Microcentrifuge Tubes | Lewis Tomlinson | Root Colonisation | View |
Preparation and Staining of Microscopy Samples | Lewis Tomlinson | Root Colonisation | View |
Planting Seeds in Agar-Filled Pipette-Tip Racks | Lewis Tomlinson | Root Colonisation | View |
Re-isolating Endophytes | Lewis Tomlinson | Root Colonisation | View |
Electroporation of Pseudomonas sp. | Frank Eardley | Endophytic Chassis Development | View |
MIC Opentrons Code (2 Plates) | Frank Eardley | Endophytic Chassis Development | View |
MIC Protocol | Frank Eardley | Endophytic Chassis Development | View |
MIC Plate Layout | Frank Eardley | Endophytic Chassis Development | View |
2-Part Gibson Assembly | Frank Eardley | Endophytic Chassis Development | View |
Amplification of gBlocks and Gradient PCR | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Colony PCR of Transformed DH5α Cells | Heather Bottomley | Naringenin Operon Biosynthesis | View |
DpnI Digestion and Purification | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Gel Extraction and Purification of the gBlocks | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Gibson Assembly of gBlocks and pSB1C3 Backbone | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Making Chemically Competent Cells | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Miniprep of Transformed Colonies | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Amplification, Purification and Quantification of the pSB1C3 Backbone by PCR | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Quantifying DNA Concentration | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Resuspending gBlocks and Primers | Heather Bottomley | Naringenin Operon Biosynthesis | View |
SOC Media Preparation | Heather Bottomley | Naringenin Operon Biosynthesis | View |
Transformation of the Gibson assembly product into pSB1C3 | Heather Bottomley | Naringenin Operon Biosynthesis | View |
References & Attributions
Attributions: Connor Trotter, Sadiya Quazi, Lewis Tomlinson, Frank Eardley, Heather Bottomley