Team:UEA-JIC Norwich/Methods

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<h1>Click on the happy scientist to open the protocol
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High Efficiency Transformation Protocol
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[[File:Happy_scientist.gif|High Efficiency Transformation Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/transformation]]
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Culture Preparation Protocol
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[[File:Happy_scientist.gif|Culture Preparation Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/cultureprep]]
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Glycerol Stock Solution Protocol
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Qiagen Miniprep Protocol
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[[File:Happy_scientist.gif|Qiagen Miniprep Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/miniprep]]
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Gel Electrophoresis Protocol
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[[File:Happy_scientist.gif|Gel Electrophoresis Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/electrophoresis]]
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PCR Protocol
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[[File:Happy_scientist.gif|PCR Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/pcr]]
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PEG Transformation Protocol
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[[File:Happy_scientist.gif|PEG Transformation Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/pegtransformation]]
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Algae Transformation using glass beads
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[[File:Happy_scientist.gif|Algae Transformation using glass beads Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/algaeglassbeads]]
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Algae Transformation using electroporation
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[[File:Happy_scientist.gif|Algae Transformation using electroporation Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/algaeelectroporation]]
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Site Directed Mutagenesis Protocol
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[[File:Happy_scientist.gif|Site Directed Mutagenesis Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/sdm]]
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pGEM T-easy Vector Cloning protocol
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[[File:Happy_scientist.gif|pGEM T-easy Vector Cloning Protocol |link=https://2011.igem.org/Team:UEA-JIC_Norwich/vectorcloning]]
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Restriction Digest protocol
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[[File:Happy_scientist.gif|Restriction Digest Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/rdigest]]
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<ul class="top">
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<li class="top-li"><a class="top-a" href="https://2011.igem.org/Team:UEA-JIC_Norwich"><b>Home</b></a>
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Poly "A" Tailing Protocol
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[[File:Happy_scientist.gif|Poly "A" Tailing PCR Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/polyatailing]]
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<li class="top-li"><a class="top-a" href="https://2011.igem.org/Team:UEA-JIC_Norwich/Team"><b>Team</b></a>
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Ligation Protocol
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[[File:Happy_scientist.gif|Ligation Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/ligation]]
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<li class="top-li"><a class="top-a down" href=""><b>Aims</b>
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Gel Extraction Protocol
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<li><a href="https://2011.igem.org/Team:UEA-JIC_Norwich/Project">Overview</a></li>
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<li><a href="https://2011.igem.org/Team:UEA-JIC_Norwich/Nittygritty">The 'Nitty Gritty'</a></li>
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[[File:Happy_scientist.gif|Gel Extraction Protocol|link=https://2011.igem.org/Team:UEA-JIC_Norwich/gelextract]]
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<li class="top-li"><a class="top-a down" href=""><b>Registry Parts</b>
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<li><a href="https://2011.igem.org/Team:UEA-JIC_Norwich/Registryoverview">Overview</a></li>
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<li><a href="https://2011.igem.org/Team:UEA-JIC_Norwich/Registrycharacterisation">Characterization</a></li>
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<li class="top-li"><a class="top-a down" href="https://2011.igem.org/Team:UEA-JIC_Norwich/Methods"><b>Methods</b>
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<li class="top-li"><a class="top-a" href="https://2011.igem.org/Team:UEA-JIC_Norwich/Safety"><b>Lab Safety</b></a>
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<li class="top-li"><a class="top-a" href="https://2011.igem.org/Team:UEA-JIC_Norwich/Follow_us"><b>Follow Us</b></a>
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<h2>High Efficiency Transformation Protocol</h2>
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<p>1. Thaw a tube of NEB 5-alpha Competent E.coli cells on ice for 10 minutes</p>
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<p>2. Mark the location of the Biobrick well (letters from top to bottom, numbers from left to right)</p>
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<p>3. Resuspend specific biobrick part (1 μl) with distilled water (20 μl). Aspirate up and down a few times</p>
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<p>4. Inoculate with DNA ( 1 μl) to the competent cells</p>
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<p>5. Place the mixture on ice for 30 minutes. Do not mix</p>
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<p>6. Heat shock at exactly 42°C for exactly 30 seconds. Do not mix</p>
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<p>7. Place on ice for 5 minutes. Do not mix</p>
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<p>8. Pipette 950 μl of room temperature SOC into the mixture</p>
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<p>9. Place at 37°C for 60 minutes. Shake vigorously (250 rpm) or rotate</p>
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<p>10. Warm selection plates to 37°C</p>
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<p>11. Do serial dilutions (2-3) at 105. Mix cells, flick/invert gently</p>
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<p>12. Spread (100 μl) on agar plates of each dilution</p>
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<p>13. Incubate overnight at 37°C</p>
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Latest revision as of 21:18, 21 September 2011

University of East Anglia-JIC

UNIVERSITY OF EAST ANGLIA-JOHN INNES CENTRE

Research methodsbanner.jpg



Click on the happy scientist to open the protocol


High Efficiency Transformation Protocol
High Efficiency Transformation Protocol
Culture Preparation Protocol
Culture Preparation Protocol
Glycerol Stock Solution Protocol
Glycerol Stock Solution Protocol
Qiagen Miniprep Protocol
Qiagen Miniprep Protocol
Gel Electrophoresis Protocol
Gel Electrophoresis Protocol
PCR Protocol
PCR Protocol
PEG Transformation Protocol
PEG Transformation Protocol
Algae Transformation using glass beads
Algae Transformation using glass beads Protocol
Algae Transformation using electroporation
Algae Transformation using electroporation Protocol
Site Directed Mutagenesis Protocol
Site Directed Mutagenesis Protocol
pGEM T-easy Vector Cloning protocol
pGEM T-easy Vector Cloning Protocol
Restriction Digest protocol
Restriction Digest Protocol
Poly "A" Tailing Protocol
Poly "A" Tailing PCR Protocol
Ligation Protocol
Ligation Protocol
Gel Extraction Protocol

Gel Extraction Protocol