Team:Newcastle/Gel extraction

Revision as of 08:13, 10 August 2010 by RachelBoyd (Talk | contribs)

Excise the DNA fragment from the agarose gel with a clean, sharp scalpel
Weight the gel slice and add 3 volumes of buffer QG to 1 volume of gel (100 mg ~ 100 µl)
Incubate at 50°C and invert the tube gently at regular intrerval until the gel has completely dissolved
After the gel has dissovled completely, check that the color of the mixture is yellow
Add 1 gel volume of isopropanol to the sample and mix
Place a QIAquick spin column in a 2 ml collection tube
To bind DNA, apple the sample to the QIAquick column and centrifuge for 1 min
Discard the flow through and place the QIAquick column back into the same tube (Maximum volumn is 750ul)
Add 0.5 ml of Buffer QG to QIAquick column and centrifuge for 1 min and discard the flow through and place the QIAquick column back into the same tube
To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min and place the QIAquick column back into the same tube
Centrifuge the column for a further 1 min
Transfer the column into a clean 1.5 ml micriocentrifuge tube
To elute DNA, add 30 µl of Buffer EB to the center of the QIAquick membrane and allow to stand for 1 min
Centrifuge the column for 1 min and transfer the eluate to a clean 1.5 ml micriocentrifuge tube