Here are your samples:

Carefully remove 10µl of each reaction (the aqueous layer beneath the mineral oil) and place in a fresh Eppendorf tube.
DO NOT TAKE UP ANY MINERAL OIL (or your sample will "float" when you try to load the gel).

To each tube, add 10µl gel loading buffer.

Load the samples on a 2% agarose gel.

Also load the 100bp "size marker" sample provided.

Remember which lane is which!

Run the gel

	Carefully remove 10µl of each reaction (the aqueous layer beneath the mineral oil) and place in a fresh Eppendorf tube. DO NOT TAKE UP ANY MINERAL OIL (or your sample will "float" when you try to load the gel).
To each tube, add 10µl gel loading buffer. Load the samples on a 2% agarose gel. Also load the 100bp "size marker" sample provided. Remember which lane is which!