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+ | </style> | ||
<h1 style="text-align:center">Experiments</h1> | <h1 style="text-align:center">Experiments</h1> | ||
+ | |||
<h2> Protocols </h2> | <h2> Protocols </h2> | ||
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<li>Add 450 microliters of LB media to the cells.</li> | <li>Add 450 microliters of LB media to the cells.</li> | ||
<li>Pellet out the cell by centrifuging at 6000 RPM for 60 seconds.</li> | <li>Pellet out the cell by centrifuging at 6000 RPM for 60 seconds.</li> | ||
− | + | <li>Remove 350 microliters of the supernatant and resuspend the cells.</li> | |
+ | <li>Pipet 100 microliters of the cells onto the appropriate plate and spread the cells throughout the plate using inoculation loops</li> | ||
+ | </ol> | ||
+ | <p><strong>Preparation of LB Media</strong></p> | ||
+ | <ol> | ||
+ | <li> Fill a container to about 70% of its volume with distilled water(assuming the container volume is the total volume of media intended to be made). </li> | ||
+ | <li> Add 10 g/L of Tryptone.</li> | ||
+ | <li> Add 10 g/L of NaCl. </li> | ||
+ | <li> Add 5 g/L of Yeast Extract. </li> | ||
+ | <li> Stir and fill up remaining volume with distilled water. </li> | ||
+ | </ol> | ||
+ | <p><strong>Preparation of LB Agar</strong></p> | ||
+ | <ol> | ||
+ | <li> Fill a container to about 60%-70% of its volume with distilled water(assuming the container volume is the total volume of media intended to be made). </li> | ||
+ | <li> Add 10 g/L of Tryptone.</li> | ||
+ | <li> Add 10 g/L of NaCl. </li> | ||
+ | <li> Add 5 g/L of Yeast Extract. </li> | ||
+ | <li> Add 20g/L of Agar.</li> | ||
+ | <li> Stir and fill up remaining volume with distilled water. </li> | ||
+ | </ol> | ||
+ | |||
+ | <p><strong>Preparation of Competent Cells/strong></p> | ||
+ | <ol> | ||
+ | <li>Thaw 50 microliters of cells on ice for 5 minutes.</li> | ||
</html> | </html> |
Revision as of 06:05, 12 June 2017
Experiments
Protocols
Transformation
- Thaw 100 microliters of competent cells on ice.
- Add 5 microliters of DNA (plasmids) to the thawed competent cells.
- Incubate the cells and DNA on ice for 30 minutes.
- Place the tubes with the cells and DNA in a 42 deg. Celsius bath for 45-60 seconds.
- Leave cells on ice for about 2-5 minutes.
- Add 450 microliters of LB media to the cells.
- Pellet out the cell by centrifuging at 6000 RPM for 60 seconds.
- Remove 350 microliters of the supernatant and resuspend the cells.
- Pipet 100 microliters of the cells onto the appropriate plate and spread the cells throughout the plate using inoculation loops
Preparation of LB Media
- Fill a container to about 70% of its volume with distilled water(assuming the container volume is the total volume of media intended to be made).
- Add 10 g/L of Tryptone.
- Add 10 g/L of NaCl.
- Add 5 g/L of Yeast Extract.
- Stir and fill up remaining volume with distilled water.
Preparation of LB Agar
- Fill a container to about 60%-70% of its volume with distilled water(assuming the container volume is the total volume of media intended to be made).
- Add 10 g/L of Tryptone.
- Add 10 g/L of NaCl.
- Add 5 g/L of Yeast Extract.
- Add 20g/L of Agar.
- Stir and fill up remaining volume with distilled water.
Preparation of Competent Cells/strong>
- Thaw 50 microliters of cells on ice for 5 minutes.