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Team:Lambert GA/NoteBook
From 2014hs.igem.org
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<li> <b>January 2014:</b> Began research into source organisms for the Chitin Deacytelase gene.</li> | <li> <b>January 2014:</b> Began research into source organisms for the Chitin Deacytelase gene.</li> | ||
<li> <b>February 2014:</b> iGEM kit arrived.</li> | <li> <b>February 2014:</b> iGEM kit arrived.</li> | ||
| - | <li> <b>March 2014:</b> Began extracting genomic yeast DNA. Used a protocol from Looke Article, Biotechnology Volume 50. using lithium acetate etc. Results were inconsistent and yields were low. | + | <li> <b>March 2014:</b> Began extracting genomic yeast DNA. Used a protocol from Looke Article, Biotechnology Volume 50. using lithium acetate etc. Results were inconsistent and yields were low.</li> |
| - | </li><b> April 2014:<b> Used Pierce Thermoscientific Yeast DNA Extraction Kit to extract genomic DNA from S.cerevisiae. PCR using pMAL primers. Began Ligations. | + | </li><b> April 2014:<b> Used Pierce Thermoscientific Yeast DNA Extraction Kit to extract genomic DNA from S.cerevisiae. PCR using pMAL primers. Began Ligations.</li> |
| - | <li><b> May 2014:<b> Continued ligations using Quick Ligation, Overnight ligation and T4ligase. Further research determined low efficiency of blunt ended ligations. | + | <li><b> May 2014:<b> Continued ligations using Quick Ligation, Overnight ligation and T4ligase. Further research determined low efficiency of blunt ended ligations.</li> |
| - | <li><b> June 2014:<b> Began Biobricking CDA gene. Designed Biobrick primers for CDA, PCR, digested, ligated with PSB1C3 and transformations with DH10beta competent cells. | + | <li><b> June 2014:<b> Began Biobricking CDA gene. Designed Biobrick primers for CDA, PCR, digested, ligated with PSB1C3 and transformations with DH10beta competent cells.</li> |
</ul> | </ul> | ||
Revision as of 22:56, 20 June 2014
Lambert iGEM NoteBook
- Lab Notes
- Fall 2013: Our team visited a local farm to determine needs in our community. From the visit, we began formulating the idea of a fruit preservative.
- November and December 2013: We began to work on sterile techniques and safety training. Also began research into Chitin to Chitosan Pathway as well as applications of chitosan.
- January 2014: Began research into source organisms for the Chitin Deacytelase gene.
- February 2014: iGEM kit arrived.
- March 2014: Began extracting genomic yeast DNA. Used a protocol from Looke Article, Biotechnology Volume 50. using lithium acetate etc. Results were inconsistent and yields were low. April 2014: Used Pierce Thermoscientific Yeast DNA Extraction Kit to extract genomic DNA from S.cerevisiae. PCR using pMAL primers. Began Ligations.
- May 2014: Continued ligations using Quick Ligation, Overnight ligation and T4ligase. Further research determined low efficiency of blunt ended ligations.
- June 2014: Began Biobricking CDA gene. Designed Biobrick primers for CDA, PCR, digested, ligated with PSB1C3 and transformations with DH10beta competent cells.
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