(6 intermediate revisions by 3 users not shown) | |||
Line 10: | Line 10: | ||
<!-- home | <!-- home | ||
================================================== --> | ================================================== --> | ||
− | <section id="home" class="s-home target-section" data-parallax="scroll" data-image-src="https://static.igem.org/mediawiki/2018/ | + | <section id="home" class="s-home target-section" data-parallax="scroll" data-image-src="https://static.igem.org/mediawiki/2018/4/4c/T--Newcastle--2345234.png"> |
<div class="overlay"></div> | <div class="overlay"></div> | ||
Line 82: | Line 82: | ||
<td>Chemotaxis</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> | <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> | ||
<tr> | <tr> | ||
Line 94: | Line 100: | ||
<td>Connor Trotter</td> | <td>Connor Trotter</td> | ||
<td>Chemotaxis</td> | <td>Chemotaxis</td> | ||
− | <td><a href="https://static.igem.org/mediawiki/2018/ | + | <td><a href="https://static.igem.org/mediawiki/2018/4/47/T--Newcastle--0.5ProtocolRedone.pdf" style="color:green">View<a/></td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
− | <td>0. | + | <td>0.50 % Agar Chemotaxis Assay</td> |
<td>Connor Trotter</td> | <td>Connor Trotter</td> | ||
<td>Chemotaxis</td> | <td>Chemotaxis</td> | ||
− | <td><a href="https://static.igem.org/mediawiki/2018/ | + | <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> | ||
<tr> | <tr> | ||
Line 111: | Line 117: | ||
<tr> | <tr> | ||
<td>Quantitative Capillary Assay</td> | <td>Quantitative Capillary Assay</td> | ||
− | <td> | + | <td>Connor Trotter</td> |
<td>Chemotaxis</td> | <td>Chemotaxis</td> | ||
− | <td><a href="https://static.igem.org/mediawiki/2018/ | + | <td><a href="https://static.igem.org/mediawiki/2018/a/a1/T--Newcastle--CapillaryAssayChemo.pdf" style="color:green">View</a></td> |
</tr> | </tr> | ||
+ | |||
<tr> | <tr> | ||
<td>Naringenin Kill Curve in Liquid Culture</td> | <td>Naringenin Kill Curve in Liquid Culture</td> | ||
Line 155: | Line 162: | ||
<td>Frank Eardley</td> | <td>Frank Eardley</td> | ||
<td>Endophytic Chassis Development</td> | <td>Endophytic Chassis Development</td> | ||
− | <td><a href="https://static.igem.org/mediawiki/2018/ | + | <td><a href="https://static.igem.org/mediawiki/2018/a/af/T--Newcastle--KillCurveCodes.pdf" style="color:green">View</a></td> |
</tr> | </tr> | ||
<tr> | <tr> |
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