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Team:BYU Provo/Notebook/Auxotrophy/SeptOct
From 2014.igem.org
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<h3>Sept 11</h3> | <h3>Sept 11</h3> | ||
<p> (TR) Checked on the growth of both the <i>N. multiformis</i> and <i>N. eutropha</i>. Neither one appears to have any growth. We cannot begin our work on <i>N eutropha</i> until be can grow enough to get a template from for PCR to make the front and back ends of our insert to knock out <i>serB</i> from the genome.</p> | <p> (TR) Checked on the growth of both the <i>N. multiformis</i> and <i>N. eutropha</i>. Neither one appears to have any growth. We cannot begin our work on <i>N eutropha</i> until be can grow enough to get a template from for PCR to make the front and back ends of our insert to knock out <i>serB</i> from the genome.</p> | ||
| + | |||
| + | <h2>Week of September 19</h2> | ||
| + | <h3>Sept 15</h3> | ||
| + | <p> (TR,CB) After collaboration, we decided to try purifying our PCR product of the front and back pieces of our eventual insert for ligation. We did this using the GFX PCR DNA and Gel Band Purification Kit. Then we ran the purified product on a gel at 120V for 30 min.</p> | ||
| + | <h3>Sept 16</h3> | ||
| + | <p> (TR) Took the purified product from yesterdy and ran SOEing PCR again with q5 polymerase. After running it on a gel, we found that it worked! We also now have <i>N multiformis</i> growing which we obtained from the University of Utah, so we can move forward with conjugation as soon as our cloning is done and the <i>N multiformis</i> has grown up enough. We are abandoning the <i>N eutropha</i> possibility since we can't obtain any genomic DNA to use as a template.</p> | ||
| + | <h3>Sept 17</h3> | ||
| + | <p> (TR,CB) Took our SOEing PCR product and the vector and did a restriction digest of each with BamHI and SpeI using the standard protocol.</p> | ||
| + | <h3>Sept 18</h3> | ||
| + | <p> (TR,CB) We ran our digested insert and vector on a low melt gel at 80V for 60 min. After cutting out the correct bands, we went straight into a ligation.</p> | ||
| + | <h3>Sept 19</h3> | ||
| + | <p> (TR) | ||
| + | |||
</html> | </html> | ||
Revision as of 21:06, 1 October 2014
BYU 2014 Notebook |
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Week of September 5
Sept 3
(TR,CB) Performed SOEing PCR on the front and back halves of insert to go into pSR47s plasmid. We used the high fidelity q5 DNA polymerase.
Sept 4
(TR) Ran our PCR product from yesterday on a gel electrophoresis to determine if the SOEing worked. The gel came out with only a band at the 500bp range, therefore we know it didn't work. This shouldn't be a problem since we are still waiting to have some N. multiformis grow to be used in conjugation.
Week of September 12
Sept 8
(TR,CB) Ran SOEing PCR again with q5 as the polymerase.
Sept 10
(TR,CB) Ran a gel electrophoresis on Monday's PCR product. Still only a band at the 500bp mark. Reviewed literature on PCR techniques and tried to figure out why our SOEing isn't working. Didn't find anything new.
Sept 11
(TR) Checked on the growth of both the N. multiformis and N. eutropha. Neither one appears to have any growth. We cannot begin our work on N eutropha until be can grow enough to get a template from for PCR to make the front and back ends of our insert to knock out serB from the genome.
Week of September 19
Sept 15
(TR,CB) After collaboration, we decided to try purifying our PCR product of the front and back pieces of our eventual insert for ligation. We did this using the GFX PCR DNA and Gel Band Purification Kit. Then we ran the purified product on a gel at 120V for 30 min.
Sept 16
(TR) Took the purified product from yesterdy and ran SOEing PCR again with q5 polymerase. After running it on a gel, we found that it worked! We also now have N multiformis growing which we obtained from the University of Utah, so we can move forward with conjugation as soon as our cloning is done and the N multiformis has grown up enough. We are abandoning the N eutropha possibility since we can't obtain any genomic DNA to use as a template.
Sept 17
(TR,CB) Took our SOEing PCR product and the vector and did a restriction digest of each with BamHI and SpeI using the standard protocol.
Sept 18
(TR,CB) We ran our digested insert and vector on a low melt gel at 80V for 60 min. After cutting out the correct bands, we went straight into a ligation.
Sept 19
(TR)
