Thursday, 21 April 2016

DNA Gel Extraction and Purification Using Columns

Spin column purification of DNA inserts from agarose gels is a quick and easy process but the downside is that yields are lower compared to DNA purified using a phenol/chloroform extraction protocol. Notwithstanding this, column purification is quite popular and the yields are sufficient for most applications. Interestingly though, there are times when there appears to be no DNA at the end of it.

Something to take note of is the size cut-off of the columns. If you plan on cloning small to very small inserts, pay attention to the kit you are using because you want to avoid having your inserts fall through the filter. Below is a list of various kits and their minimum size cut-offs:

Company
Kit
Minimum Size (bp)
Agilent Technologies
100
Merck Millipore
100
GenScript


100
Qiagen
70
Omega Bio-tek
70
Macherey-Nagel
50
Affymetrix
50
Zymo Research
50
NEB
50
Sigma-Aldrich
50
Thermo Fisher Scientific
40

It goes without saying that if you are trying to clone a 48bp insert, you probably don’t want to be using the QIAquick Gel Extraction Kit.

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