Team:SDU-Denmark/labnotes6
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Methods: | Methods: | ||
protocos: | protocos: | ||
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Notes:<br> | Notes:<br> | ||
100 mL ON culture was made, cells were grown at 37 C in LB media with Chloramphenicol. | 100 mL ON culture was made, cells were grown at 37 C in LB media with Chloramphenicol. | ||
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Done by: Marie & Tommy<br> | Done by: Marie & Tommy<br> | ||
Methods: Miniprep, Restriction digest, gel<br> | Methods: Miniprep, Restriction digest, gel<br> | ||
- | Protocols: | + | Protocols: [https://2010.igem.org/Team:SDU-Denmark/protocols#MP1.2 MP1.2], [https://2010.igem.org/Team:SDU-Denmark/protocols#RD1.1 RD1.1]. |
- | + | ||
Notes:<br> | Notes:<br> | ||
50 mL of elution buffer was used. DNA concentrations after pooling were measured on NanoDrop to 206,2 ng/microL. | 50 mL of elution buffer was used. DNA concentrations after pooling were measured on NanoDrop to 206,2 ng/microL. | ||
gel was run on produckt, showing recent miniprep compared to old miniprep produckt, showing uneven lengths. subsequent was performed.<br> | gel was run on produckt, showing recent miniprep compared to old miniprep produckt, showing uneven lengths. subsequent was performed.<br> | ||
- | [[Image:Team-sdu-denmark-Minipreb_product_of_POT2_with_NinaB_1,5_gel_red_loader__-4.jpg | | + | [[Image:Team-sdu-denmark-Minipreb_product_of_POT2_with_NinaB_1,5_gel_red_loader__-4.jpg | 300px ]] |
==== Restriction digest on miniprep produckt (w. EcoRI) ==== | ==== Restriction digest on miniprep produckt (w. EcoRI) ==== | ||
Date: 17/8<br> | Date: 17/8<br> | ||
Done by: Marie & Tommy<br> | Done by: Marie & Tommy<br> | ||
Methods: Restriction digest, gel<br> | Methods: Restriction digest, gel<br> | ||
- | Protocols: | + | Protocols: [https://2010.igem.org/Team:SDU-Denmark/protocols#MP1.2 MP1.2], gel. |
- | + | ||
Notes:<br> | Notes:<br> | ||
Due to the lack of old sample, restriction digest was performed using only 3,5 microL of miniprep produckt. 1,5 microL of H2O was added insted. EcoRI was used<br> | Due to the lack of old sample, restriction digest was performed using only 3,5 microL of miniprep produckt. 1,5 microL of H2O was added insted. EcoRI was used<br> | ||
The digest mix was incubated for 10 min at 37 C. A gel was run showing uncut new, cut new, uncut old and cut old miniprep product.<br> | The digest mix was incubated for 10 min at 37 C. A gel was run showing uncut new, cut new, uncut old and cut old miniprep product.<br> | ||
- | [[Image:Team-sdu-denmark-Minipreb_product_of_POT2_with_NinaB_1,5_gel_red_loader__-5.jpg | | + | [[Image:Team-sdu-denmark-Minipreb_product_of_POT2_with_NinaB_1,5_gel_red_loader__-5.jpg |300px ]] |
+ | |||
+ | === PCR on POT2 with NinaB (New Primers) === | ||
+ | Start date: 20/8<br> | ||
+ | Methods: PCR, Gel<br> | ||
+ | Protocols: [https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP.1.1] | ||
+ | |||
+ | ==== PCR on POT2 with NinaB (New Primers) ==== | ||
+ | Date: 20/8<br> | ||
+ | Done by: Marie & Tommy<br> | ||
+ | Methods: ON<br> | ||
+ | protocos:[https://2010.igem.org/Team:SDU-Denmark/protocols#CP1.1 CP1.1] | ||
+ | Notes:<br> | ||
+ | The new primers only contain the innermost restriction sites.<br> | ||
+ | Meltting temp.: FWD: 68,1 C REV: 65,6 C<br> | ||
+ | To get the optimal PCR temperatures a gradient PCR were run programed as:<br> | ||
+ | <html> | ||
+ | <head> | ||
+ | <meta content="text/html; charset=ISO-8859-1" | ||
+ | http-equiv="content-type"> | ||
+ | <title></title> | ||
+ | </head> | ||
+ | <body> | ||
+ | <table style="text-align: left; width: 300px;" border="1" | ||
+ | cellpadding="2" cellspacing="2"> | ||
+ | <tr> | ||
+ | <td>PCR</td> | ||
+ | <td>Temp. (C)</td> | ||
+ | <td>Time (min)</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Start</td> | ||
+ | <td>95</td> | ||
+ | <td>2</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Denaturing</td> | ||
+ | <td>95</td> | ||
+ | <td>1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Anneling</td> | ||
+ | <td>Gradient</td> | ||
+ | <td>1</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Elongation</td> | ||
+ | <td>72</td> | ||
+ | <td>4</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>End</td> | ||
+ | <td>72</td> | ||
+ | <td>5</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>Hold</td> | ||
+ | <td>4</td> | ||
+ | <td>indef.</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <br> | ||
+ | </body> | ||
+ | </html> | ||
+ | <br> | ||
+ | The temperatur gradient were run from 60 to 70 C and the samples were run at these temperatures:<br> | ||
+ | <html> | ||
+ | <head> | ||
+ | <meta content="text/html; charset=ISO-8859-1" | ||
+ | http-equiv="content-type"> | ||
+ | <title></title> | ||
+ | </head> | ||
+ | <body> | ||
+ | <table style="text-align: left; width: 300px;" border="1" | ||
+ | cellpadding="2" cellspacing="2"> | ||
+ | <tr> | ||
+ | <td>Sample</td> | ||
+ | <td>Colunm</td> | ||
+ | <td>Temp. C</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>1</td> | ||
+ | <td>1</td> | ||
+ | <td>59,9</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>2</td> | ||
+ | <td>3</td> | ||
+ | <td>60,7</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>3</td> | ||
+ | <td>5</td> | ||
+ | <td>62,7</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>4</td> | ||
+ | <td>7</td> | ||
+ | <td>65,4</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>5</td> | ||
+ | <td>9</td> | ||
+ | <td>67,9</td> | ||
+ | </tr> | ||
+ | <tr> | ||
+ | <td>6</td> | ||
+ | <td>11</td> | ||
+ | <td>69,6</td> | ||
+ | </tr> | ||
+ | </table> | ||
+ | <br> | ||
+ | </body> | ||
+ | </html><br> | ||
+ | After the PRC the product were run on a gel<br> | ||
+ | |||
+ | The gel picture shows that alle of the temperatures gave results. |
Latest revision as of 22:21, 23 October 2010