Team:IPN-UNAM-Mexico/Notebook/August 11 2009
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+ | <tr> | ||
+ | <td><p> </p> | ||
+ | <p><strong>August 11th, 2009</strong></p> | ||
+ | <p>Amplification of the promoter and RBS using plasmidic DNA from Q04121.</p> | ||
+ | <blockquote> | ||
+ | <p>Digestion Mix<br> | ||
+ | PlasmidicDNA 4.0 μl (= 1 μg DNA) x 20 = 80 μl<br> | ||
+ | BSA 0.5 μl x 20 = 10 μl<br> | ||
+ | Buffer 2 1.0 μl x 20 = 20 μl<br> | ||
+ | Enzyme EcoRI 0.5 μl x 20 = 10 μl<br> | ||
+ | H2O 4.0 μl x 20 = 80 μl <br> | ||
+ | Cf 10.0 μl 200 μl</p> | ||
+ | </blockquote> | ||
+ | <p> </p> | ||
+ | <p>Load order:</p> | ||
+ | <blockquote> | ||
+ | <p>Well Plasmid<br> | ||
+ | 2 2:3 L1<br> | ||
+ | 3 2:3 L2’<br> | ||
+ | 4 2:3 L2”<br> | ||
+ | 5 15:13<br> | ||
+ | 6 15:3<br> | ||
+ | 7 4:23<br> | ||
+ | 8 4:23 L2</p> | ||
+ | </blockquote> | ||
+ | <p> </p> | ||
+ | <blockquote> | ||
+ | <p> <strong>Gel 7:31 pm</strong><br> | ||
+ | Well Plasmid Well Plasmid<br> | ||
+ | 1 Marker 1 Marker<br> | ||
+ | 2 2_3L2#1 2 9.1<br> | ||
+ | 3 2:3L2#2 3 9.3<br> | ||
+ | 4 2_3L2#3 4 9.4<br> | ||
+ | 5 3.3* 5 9.5<br> | ||
+ | 6 4_23L1 6 9.6<br> | ||
+ | 7 No 4_23L2 7 9.7<br> | ||
+ | 8 7.3 8 9.8<br> | ||
+ | 9 11.1 9 9.9<br> | ||
+ | 10 14.2 10 9.10<br> | ||
+ | 11 15.3 11 Marker<br> | ||
+ | 12 15_13L2 #1 12 ----------<br> | ||
+ | 13 15_13L2 #2 Digest with EcoRI<br> | ||
+ | 14 15_13L2 #3 at 4°C<br> | ||
+ | 15 16.2” Digest with EcoRI<br> | ||
+ | 16 18.2*<br> | ||
+ | 17 19.1* Repeat digestion –DNA<br> | ||
+ | 18 22.1* Repeat digestion-DNA<br> | ||
+ | 19 24.2” Repeat digestion – DNA<br> | ||
+ | 20 Marker</p> | ||
+ | <p> Note: it is needed to digest lesser the plasmid 11.1.</p> | ||
+ | </blockquote> | ||
+ | <p> </p> | ||
+ | <p>Repeat digestions of the plasmids:</p> | ||
+ | <ul> | ||
+ | <li>19.1 </li> | ||
+ | <li>22.1</li> | ||
+ | <li>24.2</li> | ||
+ | </ul> | ||
+ | <p>which are at -20°C in the Unicel (with 3μl of DNA) and the 9 is at 4°C.<br> | ||
+ | Put 3 μl of DNA and 5 μl of water.<br> | ||
+ | Digestion Mix x 10.</p> | ||
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