Difference between revisions of "Team:Macquarie Australia/Notebook"
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font-family: 'Quicksand', sans-serif; | font-family: 'Quicksand', sans-serif; | ||
} | } | ||
| + | |||
| + | /*dot points for each week*/ | ||
| + | ul.normal { | ||
| + | list-style-type: bullet; | ||
| + | font-size: 14px; | ||
| + | font-family: 'Quicksand', sans-serif; | ||
| + | } | ||
| + | /*dot points for each week - indented*/ | ||
| + | ul.indented { | ||
| + | list-style-type: circle; | ||
| + | font-size: 14px; | ||
| + | font-family: 'Quicksand', sans-serif; | ||
| + | } | ||
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#accordion section p { | #accordion section p { | ||
display: none; | display: none; | ||
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</h> | </h> | ||
<p style="text-align: justify; font-size: 14px;"> | <p style="text-align: justify; font-size: 14px;"> | ||
| − | < | + | <ul class="normal"> |
<!-- ENTER TEXT FOR THE PAGE HERE --> | <!-- ENTER TEXT FOR THE PAGE HERE --> | ||
| + | <li> | ||
We went through lab safety induction to ensure safety procedures were followed at all times in the lab | We went through lab safety induction to ensure safety procedures were followed at all times in the lab | ||
</li> | </li> | ||
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We learnt how to perform digestion, ligation, transformation and how to make and run agarose gels | We learnt how to perform digestion, ligation, transformation and how to make and run agarose gels | ||
</li> | </li> | ||
| + | <li> | ||
We used digestion to screen the Photosystem II (PSII) parts DCA, psbELJTB and psbMZtlwkOPQR. psbELJTB and psbMZtlwkOPQR showed successful digestion and correct sizes. DCA showed signs of contamination in all samples. | We used digestion to screen the Photosystem II (PSII) parts DCA, psbELJTB and psbMZtlwkOPQR. psbELJTB and psbMZtlwkOPQR showed successful digestion and correct sizes. DCA showed signs of contamination in all samples. | ||
| − | + | </li> | |
| + | <li> | ||
We decided to focus of the Chlorophyll plasmid rather than PS II. We proceeded with digestion and ligation of ChlD with ChlI2 as well as DRV1 with ChlG, both into Kanamycin backbones, following the 3A assembly protocol. | We decided to focus of the Chlorophyll plasmid rather than PS II. We proceeded with digestion and ligation of ChlD with ChlI2 as well as DRV1 with ChlG, both into Kanamycin backbones, following the 3A assembly protocol. | ||
| − | + | </li> | |
| + | <li> | ||
Renee, Areti and Karl also began the interlab study: | Renee, Areti and Karl also began the interlab study: | ||
| − | + | </li> | |
| + | </ul> | ||
Revision as of 14:15, 6 October 2018
Project planning - no wet lab work this week.
- We went through lab safety induction to ensure safety procedures were followed at all times in the lab
- We learnt how to perform digestion, ligation, transformation and how to make and run agarose gels
- We used digestion to screen the Photosystem II (PSII) parts DCA, psbELJTB and psbMZtlwkOPQR. psbELJTB and psbMZtlwkOPQR showed successful digestion and correct sizes. DCA showed signs of contamination in all samples.
- We decided to focus of the Chlorophyll plasmid rather than PS II. We proceeded with digestion and ligation of ChlD with ChlI2 as well as DRV1 with ChlG, both into Kanamycin backbones, following the 3A assembly protocol.
- Renee, Areti and Karl also began the interlab study:
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