Make and run an agarose gel: Difference between revisions
From London Hackspace Wiki
Mycoplasma (talk | contribs) (Created page with "=== Make gel === * Choose the gel concentration (higher the concentration the smaller the bands you can see). The following instructions are for a 1% of 50ml, which we normally ...") |
Mycoplasma (talk | contribs) |
||
Line 3: | Line 3: | ||
* Choose the gel concentration (higher the concentration the smaller the bands you can see). The following instructions are for a 1% of 50ml, which we normally use. | * Choose the gel concentration (higher the concentration the smaller the bands you can see). The following instructions are for a 1% of 50ml, which we normally use. | ||
* Add 1 gram of agarose to 5g (or ml) of TBE 10x and 45g (or ml) of dH20. | * Add 1 gram of agarose to 5g (or ml) of TBE 10x and 45g (or ml) of dH20. | ||
* Mix and then microwave this until it is clear (normally around 1 min) | |||
* Leave to cool, then add Ethidium Bromide stock solution at a concentration of 2ul/40ml (so about 2.25ul for this gel) at about 50°C. |
Revision as of 20:05, 4 September 2012
Make gel
- Choose the gel concentration (higher the concentration the smaller the bands you can see). The following instructions are for a 1% of 50ml, which we normally use.
- Add 1 gram of agarose to 5g (or ml) of TBE 10x and 45g (or ml) of dH20.
- Mix and then microwave this until it is clear (normally around 1 min)
- Leave to cool, then add Ethidium Bromide stock solution at a concentration of 2ul/40ml (so about 2.25ul for this gel) at about 50°C.