Team:Washington/HOMEPAGE PROTOCOL
From 2013.igem.org
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+ | <u>Cloning Protocols Workflow</u> | ||
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+ | Tips and Etiquette: | ||
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+ | <li><a href = "https://2013.igem.org/T<html> | ||
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<li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">General Basic Protocol Information</a></li> | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">General Basic Protocol Information</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">How to Label EVERYTHING</a></li> | ||
+ | </ul> | ||
+ | Keep notebooks up-to-date | ||
+ | </p> | ||
+ | |||
+ | <p> | ||
+ | Workflow: | ||
+ | <ul> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">Primer Design</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/HOW_TO_LABEL_EVERYTHING">Streaking a Plate for Isolation</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">Overnight Cultures</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">1) Isolation of Plasmid DNA (miniprep)</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">2) General PCR Protocol </a>(also see <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">PCR GoTag</a> - product (30-200ng/ ul) Check on gel PCR Purification and/or <a href = "">Dpnl Digest</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">3) General Digestion Protocol</a> Check on gel PCR Purification or Heat Inactivation (check enzyme temp and time, usually 80C for 20min)</li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">4) Agarose Gel Electrophoresis</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">5) General Ligation Protocol</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">6) Heat shock/chemical competent transformation</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">7) Colony PCR with Green taq</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">8) DNA Sequencing</a></li> | ||
+ | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">9) Making Glycerol Frozen Stocks</a></li> | ||
+ | </ul> | ||
+ | </p> | ||
+ | |||
+ | <br> | ||
+ | <p1> | ||
+ | I AM PARAGRPAHIRGJIG 2 | ||
+ | </p1> | ||
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+ | </body> | ||
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+ | </html> | ||
+ | eam:Washington/GENERAL_BASIC_PROTOCOL">General Basic Protocol Information</a></li> | ||
<li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">How to Label EVERYTHING</a></li> | <li><a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">How to Label EVERYTHING</a></li> | ||
</ul> | </ul> |
Revision as of 01:51, 7 September 2013
Tips and Etiquette:
Keep notebooks up-to-dateWorkflow:
- Primer Design
- Streaking a Plate for Isolation
- Overnight Cultures
- 1) Isolation of Plasmid DNA (miniprep)
- 2) General PCR Protocol (also see PCR GoTag - product (30-200ng/ ul) Check on gel PCR Purification and/or Dpnl Digest
- 3) General Digestion Protocol Check on gel PCR Purification or Heat Inactivation (check enzyme temp and time, usually 80C for 20min)
- 4) Agarose Gel Electrophoresis
- 5) General Ligation Protocol
- 6) Heat shock/chemical competent transformation
- 7) Colony PCR with Green taq
- 8) DNA Sequencing
- 9) Making Glycerol Frozen Stocks
Workflow:
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">Primer Design</a>
- <a href = "https://2013.igem.org/Team:Washington/HOW_TO_LABEL_EVERYTHING">Streaking a Plate for Isolation</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">Overnight Cultures</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">1) Isolation of Plasmid DNA (miniprep)</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">2) General PCR Protocol </a>(also see <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">PCR GoTag</a> - product (30-200ng/ ul) Check on gel PCR Purification and/or <a href = "">Dpnl Digest</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">3) General Digestion Protocol</a>Check on gel PCR Purification or Heat Inactivation (check enzyme temp and time, usually 80C for 20min)
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">4) Agarose Gel Electrophoresis</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">5) General Ligation Protocol</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">6) Heat shock/chemical competent transformation</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">7) Colony PCR with Green taq</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">8) DNA Sequencing</a>
- <a href = "https://2013.igem.org/Team:Washington/GENERAL_BASIC_PROTOCOL">9) Making Glycerol Frozen Stocks</a>
<p1>
I AM PARAGRPAHIRGJIG 2
</p1>
</body>
</html>