QIAquick Gel Extraction
Posted 06 September 2012 - 03:49 AM
I have a small doubt regarding the gel extraction purification. I cut of my fragment from the agarose and after weighing the weight of my fragments are 460mg and 550mg..but the Extraction kit says for the slice of more than 400mg we should use more than one QIA column.I have never used in such conditions.You can anyone suggest me how to proceed with my extraction. I am unable to figure it out..
Quick reply would be really appreciated..
Posted 06 September 2012 - 06:34 AM
Next times maybe try to cut smaller agarose slices.
Posted 06 September 2012 - 03:52 PM
The column is primarily limited by the amount of DNA, which is the same for small and big slice, but also by the amount of agarose that has to go throught the column. Maybe I would put there even more than 3x QG buffer to disolve the agarose even more than usual. You will need to centrifuge it repeatedly since there is only space for 800 ul in the column, maybe wash it with QG buffer after each spin, in addition to the final wash, so that the agarose will less likely clogg the column.
Our country has a serious deficiency in lighthouses. I assume the main reason is that we have no sea.
I never trust anything that can't be doubted.
'Normal' is a dryer setting. - Elizabeth Moon