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+ | <h1>Cloning Troubleshooting</h1> | ||
+ | <p>Welcome to the troubleshooting hub! Below are some helpful tips and troubleshooting strategies for common cloning problems in <i>E. coli</i>.</p> | ||
+ | <p> | ||
+ | Cloning is difficult. No one who has ever picked up a pipette in the lab would debate this fact. However, cloning shouldn't be impossible! This page exists to help students and teams who are struggling with cloning and other molecular techniques. Treat this page as another resource in your troubleshooting endeavors rather than the be-all, end-all resource for iGEM cloning problems. I hope this will be a helpful resource for every iGEM team! | ||
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<h3>Learn about cloning troubleshooting here!</h3> | <h3>Learn about cloning troubleshooting here!</h3> | ||
<ul> | <ul> | ||
<li>Read about General Tips and Tricks with a focus on: </li> | <li>Read about General Tips and Tricks with a focus on: </li> | ||
− | <ul><li | + | <ul><li>Bacterial Transformations</li> |
− | <li | + | <li>Restriction Digests and Ligations</li> |
+ | </ul><br> | ||
<li>Still have a cloning problem? Contact Traci and ask a question (see right box for contact info)!</li> | <li>Still have a cloning problem? Contact Traci and ask a question (see right box for contact info)!</li> | ||
<li>Make sure that you also ask your instructors and more experienced students around you!</li> | <li>Make sure that you also ask your instructors and more experienced students around you!</li> | ||
</ul> | </ul> | ||
+ | </div></div> | ||
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+ | <div class="column fourth_size"> | ||
+ | <h3>Welcome!</h3> | ||
+ | <p>My name is Traci, and I'm here to help you with your cloning problems. <br><br> | ||
+ | You can contact me: <ol> | ||
+ | <li><i>traci AT igem DOT org</i></li> | ||
+ | <li><a href="http://twitter.com/Traci_H_Angelli">@Traci_H_Angelli</a> </li></ol> | ||
+ | </p> | ||
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+ | <div class="column fourth_size"> | ||
+ | <img src="https://static.igem.org/mediawiki/igem.org/7/72/HQ_TraciHaddock_2016_crop_small1.jpg" > | ||
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− | < | + | <h3>General Tips and Tricks</h3> |
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+ | <a href="https://2017.igem.org/Resources/Troubleshooting/Transformations"> | ||
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<h3>Transformation Problems</h3> | <h3>Transformation Problems</h3> | ||
− | <p>For many teams, cloning problems center around transformation | + | <p>For many teams, cloning problems center around <a href="https://2017.igem.org/Resources/Troubleshooting/Transformations">transformation</a> problems. Here I describe some general tips that can be applied to any type of assembly method when using <i>E. coli</i> cells as the transformation host.</p> |
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<h3>Restriction Digest and Ligation Problems</h3> | <h3>Restriction Digest and Ligation Problems</h3> | ||
− | <p>Since we provide teams with nearly 2,000 BioBricks parts, I will discuss common problems students can experience when using restriction enzymes and DNA ligation assemblies, which includes BioBricks Assembly. </p> | + | <p>Since we provide teams with nearly 2,000 BioBricks parts, I will discuss common problems students can experience when using <a href="https://2017.igem.org/Resources/Troubleshooting/Restriction_Digests_and_Ligations"> restriction enzymes and DNA ligation assemblies</a>, which includes BioBricks Assembly. </p> |
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− | + | <h3>iGEM Protocols</h3> | |
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<p> | <p> | ||
Below are the links to the various protocols that iGEM Headquarters has provided over the years. These protocols can also be found through the Parts Registry page under the "Help" and "Protocols" links in the black toolbar at the top of the page. These are another useful resource that teams should read through when they're experiencing cloning problems. | Below are the links to the various protocols that iGEM Headquarters has provided over the years. These protocols can also be found through the Parts Registry page under the "Help" and "Protocols" links in the black toolbar at the top of the page. These are another useful resource that teams should read through when they're experiencing cloning problems. | ||
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<h5>BioBrick Cloning Protocols</h5> | <h5>BioBrick Cloning Protocols</h5> | ||
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<h5>Other Protocols for Molecular Techniques</h5> | <h5>Other Protocols for Molecular Techniques</h5> | ||
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Latest revision as of 16:00, 11 July 2017
Cloning Troubleshooting
Welcome to the troubleshooting hub! Below are some helpful tips and troubleshooting strategies for common cloning problems in E. coli.
Cloning is difficult. No one who has ever picked up a pipette in the lab would debate this fact. However, cloning shouldn't be impossible! This page exists to help students and teams who are struggling with cloning and other molecular techniques. Treat this page as another resource in your troubleshooting endeavors rather than the be-all, end-all resource for iGEM cloning problems. I hope this will be a helpful resource for every iGEM team!
Learn about cloning troubleshooting here!
- Read about General Tips and Tricks with a focus on:
- Bacterial Transformations
- Restriction Digests and Ligations
- Still have a cloning problem? Contact Traci and ask a question (see right box for contact info)!
- Make sure that you also ask your instructors and more experienced students around you!
Welcome!
My name is Traci, and I'm here to help you with your cloning problems.
You can contact me:
- traci AT igem DOT org
- @Traci_H_Angelli
General Tips and Tricks
Transformation Problems
For many teams, cloning problems center around transformation problems. Here I describe some general tips that can be applied to any type of assembly method when using E. coli cells as the transformation host.
Restriction Digest and Ligation Problems
Since we provide teams with nearly 2,000 BioBricks parts, I will discuss common problems students can experience when using restriction enzymes and DNA ligation assemblies, which includes BioBricks Assembly.
iGEM Protocols
Below are the links to the various protocols that iGEM Headquarters has provided over the years. These protocols can also be found through the Parts Registry page under the "Help" and "Protocols" links in the black toolbar at the top of the page. These are another useful resource that teams should read through when they're experiencing cloning problems.