Team:Bielefeld-CeBiTec/Notebook/Journal/rMFC/Aug
From 2014.igem.org
(Difference between revisions)
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+ | <ul> | ||
+ | <li><b><i>pR6K</i></b></li> | ||
+ | <ul> | ||
+ | <li> The <i>pR6K</i>-cassette for the <i>dcuB</i> deletion was <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">purified</a> out of the gel</li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | <ul> | ||
+ | <li><b><i>ccm</i></b></li> | ||
+ | <ul> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> of the ccm-backbone (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#pSB1C3_suf_ccm" target="_blank">pSB1C3_suf_ccm</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#pSB1C3_pre_ccm" target="_blank">pSB1C3_pre_ccm</a>)</li> | ||
+ | <ul> | ||
+ | <li>Annealing temperature: 65 °C</li> | ||
+ | <li>Bands as expected (~ bp) but slightly visible because of inappropriate annealing temperature</li> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> was repeated with an annealing temperature of 55 °C </li> | ||
+ | <li>Both PCR products were <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">purified</a> out of the gel</li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | <ul> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> of <i>ccm</i>-cassette using a gradient (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#ccm_fwd" target="_blank">ccm_fwd</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#ccm_rev" target="_blank">ccm_rev</a>)</li> | ||
+ | <ul> | ||
+ | <li>Annealing temperature: 61 °C appeared as the optimum</li> | ||
+ | <li>Bands as expected (~6281 bp)</li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | <ul> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> of <i>ccm</i>-cassette (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#ccm_fwd" target="_blank">ccm_fwd</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#ccm_rev" target="_blank">ccm_rev</a>)</li> | ||
+ | <ul> | ||
+ | <li>Annealing temperature: 61 °C</li> | ||
+ | <li>Bands as expected (~6281 bp)</li> | ||
+ | <li>PCR product was <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">purified</a></li> | ||
+ | |||
+ | </ul> | ||
+ | </ul> | ||
+ | <ul> | ||
+ | <li><b><i>GSU 3274</i></b></li> | ||
+ | <ul> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification of <i>GSU 3274</i>-backbone</a> (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#pSB1C3_pre_pccH" target="_blank">pSB1C3_pre_pccH</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#pSB1C3_suf_pccH" target="_blank">pSB1C3_suf_pccH</a>)</li> | ||
+ | <ul> | ||
+ | <li>Annealing temperature: 65 °C</li> | ||
+ | <li>Bands not as expected (~2070 bp) because of inappropriate annealing temperature</li> | ||
+ | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> was repeated with an annealing temperature of 55 °C </li> | ||
+ | <ul> | ||
+ | <li>Bands as expected (~2070 bp)</li> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | </ul> | ||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
+ | |||
</div> | </div> | ||
</div> | </div> |
Revision as of 20:39, 1 October 2014
August |
- pR6K
- PCR amplification of pR6K-cassette
- Plasmid isolation of pR6K-cassette and Purification out of the gel
- Connection of the pR6K-cassette and oprF
- PCR amplification to connect the pR6K-cassette and oprF
- Bands as expected (~3300 bp)
- PCR product was purified out of the gel
- Fum A
- Plasmid isolation of Fum A
- BioBrick Assembly (Suffix)
- Transformation of Fum A with electrocompotetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands (not) as expected (~... bp)
- BioBrick Assembly (Suffix)
- pR6K
- The pR6K-cassette for the dcuB deletion was purified out of the gel
- ccm
- PCR amplification of the ccm-backbone (pSB1C3_suf_ccm, pSB1C3_pre_ccm)
- Annealing temperature: 65 °C
- Bands as expected (~ bp) but slightly visible because of inappropriate annealing temperature
- PCR amplification was repeated with an annealing temperature of 55 °C
- Both PCR products were purified out of the gel
- PCR amplification of ccm-cassette using a gradient (ccm_fwd, ccm_rev)
- Annealing temperature: 61 °C appeared as the optimum
- Bands as expected (~6281 bp)
- PCR amplification of ccm-cassette (ccm_fwd, ccm_rev)
- Annealing temperature: 61 °C
- Bands as expected (~6281 bp)
- PCR product was purified
- GSU 3274
- PCR amplification of GSU 3274-backbone (pSB1C3_pre_pccH, pSB1C3_suf_pccH)
- Annealing temperature: 65 °C
- Bands not as expected (~2070 bp) because of inappropriate annealing temperature
- PCR amplification was repeated with an annealing temperature of 55 °C
- Bands as expected (~2070 bp)