Results
We ran a 1% gel of the digest before and after purification. We had a decent yield, maybe 40% of our initial digest product in the purified lanes.
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<h2>What is the Open Lab?</h2> | <h2>What is the Open Lab?</h2> | ||
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- | <p> | + | <h1 class='firstHeading'>Part:BBa_K1429002</h1> <div style= 'position: relative;font-size:95%;line-height:100%;'> |
- | + | Designed by: Christal Gordon Group: iGEM14_Genspace (2014-09-29)</div> | |
- | <ul> | + | <div style='height:1em;'></div> <div id="bodyContent"> |
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- | + | <p><SPAN style='font-size: 150%; font-weight: bold;'>Cyan Fluorescent Protein (CFP) "Cindy Lou" coding region, intellectual property-free</SPAN> | |
- | <p>The | + | </p><p>IP free cyan fluorescent protein. We have a ribosome binding site (RBS). |
- | + | </p> | |
- | <p> | + | <h4> <span class="mw-headline" id="Background">Background</span></h4> |
+ | <div class="entry-results"><p>We want to take Tuesday's PCR products and put them into the pSB1C3 backbone. </p> | ||
+ | <p><strong>Digest PCRs:</strong></p> | ||
+ | <p>10 ul PCR product</p> | ||
+ | <p>2 ul cutsmart buffer (10x stock)</p> | ||
+ | <p>1 ul PstI</p> | ||
+ | <p><u>1 ul EcoRI</u></p> | ||
+ | <p>20 ul total --> incubate for 30 min at 37C</p> | ||
+ | <p> </p> | ||
+ | <p><strong>PCR purify digest product (only 14 ul - save 6 ul):</strong></p> | ||
+ | <p>Follow kit protocol. Elute in elution buffer.</p> | ||
+ | <p>Worried that the washed columns won't bind DNA, we are going to use some of the set-aside (unpurified) digest product for a backup ligation. We'll run a gel of our purification, but we are going to set up a ligation beforehand, so we won't have even rough estimates of DNA concentrations.</p> | ||
+ | <p>Set up ligations:</p> | ||
+ | <table style="width: 500px;"> | ||
+ | <tbody> | ||
+ | <tr> | ||
+ | <td><strong>Component</strong></td> | ||
+ | <td><strong>Using purified digest product</strong></td> | ||
+ | <td><strong>Using unpurified digest product</strong></td> | ||
+ | <td><strong>BB alone</strong></td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>dH2O</td> | ||
+ | <td>x</td> | ||
+ | <td>11</td> | ||
+ | <td>14</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Insert (RFP or GFP)</td> | ||
+ | <td>14</td> | ||
+ | <td>3</td> | ||
+ | <td>x</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>1:10 BB</td> | ||
+ | <td>3</td> | ||
+ | <td>3</td> | ||
+ | <td>3</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>T4 buffer (10</td> | ||
+ | <td>1</td> | ||
+ | <td>1</td> | ||
+ | <td>1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td> </td> | ||
+ | <td> </td> | ||
+ | <td> </td> | ||
+ | <td> </td> | ||
+ | </tr> | ||
+ | </tbody> | ||
+ | </table> | ||
+ | <p>The above were incubated 30 min at RT then stored at -20C.</p> | ||
+ | <p> </p> | ||
+ | </div> | ||
+ | <p><br /> | ||
+ | </div> | ||
+ | </p> | ||
+ | <div class="entry"> | ||
+ | <h4> <span class="mw-headline" id="Results">Results</span></h4> | ||
+ | <div class="entry-results"><p>We ran a 1% gel of the digest before and after purification. We had a decent yield, maybe 40% of our initial digest product in the purified lanes. </p> | ||
+ | </div> | ||
+ | <p><br /> | ||
+ | </p> | ||
+ | </div> | ||
+ | <div class="entry"> | ||
+ | <h4> <span class="mw-headline" id="Conclusions">Conclusions</span></h4> | ||
+ | <div class="entry-results"><p>Next step: Transform the ligated plasmids into E. coli!</p> | ||
+ | </div> | ||
+ | <p><br /> | ||
+ | </p> | ||
+ | </div> | ||
+ | <p><br /> |
|
Cyan Fluorescent Protein (CFP) "Cindy Lou" coding region, intellectual property-free
IP free cyan fluorescent protein. We have a ribosome binding site (RBS).
We want to take Tuesday's PCR products and put them into the pSB1C3 backbone.
Digest PCRs:
10 ul PCR product
2 ul cutsmart buffer (10x stock)
1 ul PstI
1 ul EcoRI
20 ul total --> incubate for 30 min at 37C
PCR purify digest product (only 14 ul - save 6 ul):
Follow kit protocol. Elute in elution buffer.
Worried that the washed columns won't bind DNA, we are going to use some of the set-aside (unpurified) digest product for a backup ligation. We'll run a gel of our purification, but we are going to set up a ligation beforehand, so we won't have even rough estimates of DNA concentrations.
Set up ligations:
Component | Using purified digest product | Using unpurified digest product | BB alone |
dH2O | x | 11 | 14 |
Insert (RFP or GFP) | 14 | 3 | x |
1:10 BB | 3 | 3 | 3 |
T4 buffer (10 | 1 | 1 | 1 |
The above were incubated 30 min at RT then stored at -20C.
</div>
We ran a 1% gel of the digest before and after purification. We had a decent yield, maybe 40% of our initial digest product in the purified lanes.
Next step: Transform the ligated plasmids into E. coli!