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How to improve yield in DNA-purification from agars electrophoresis?

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#1 Biologystudent



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Posted 29 March 2014 - 12:07 PM

As title states, how can I improve the yield?

I go from 300ng/ul down to barely 20ng/ul.

I tried to incubate longer time at RT (too evaporate the ethanol from the washing step, but at the same time not too long to risk getting over-dried). Also tried to centrifuge at higher speed and for 2min. And to divide my elution down to 2steps (first 20ul and then 10ul).

Not much improvement so far.

I am using Ge Healthcare Illustra Agaros Purification Kit.


#2 bob1


    Thelymitra pulchella

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Posted 29 March 2014 - 03:04 PM

There isn't a whole lot that you can do - yields of 10% or less are very common with gel extractions.  The reason is that agarose is a sugar based molecule similar to DNA, so separating the two is quite hard.

#3 perneseblue


    Unlimited ligation works!

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Posted 30 March 2014 - 06:56 AM

You can do a few things

1 - increase the amount of capture buffer you are using. Increase by 50%.

2 - you can pass the capture buffer through the column two or three times.

3 - you can add isopropanol to the (capture buffer + agarose) solution  (100ul for every 300ul)

4 - you can use warm elution buffer.

5 - you can do two elutions (which you have already done).


but that said, you do take hit from using a column.

May your PCR products be long, your protocols short and your boss on holiday

#4 hobglobin


    Growing old is mandatory, growing up is optional...

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Posted 30 March 2014 - 09:12 AM

Also have a look on older threads, this is a common problem:


http://www.protocol-...gel +extraction

http://www.protocol-...gel +extraction


and so on...

One must presume that long and short arguments contribute to the same end. - Epicurus
...except casandra's that belong to the funniest, most interesting and imaginative (or over-imaginative?) ones, I suppose.

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