Extracting DNA from low-melt agarose gels

John H McDonald mcdonald at ravel.udel.edu
Fri Jul 9 13:50:10 EST 1993


In article <01H0AHG3K9OY8WW9E0 at Butler.EDU> KARN at Butler.EDU writes:
>I wish to use low-melt agarose gels to clean up a PCR product of about 1 kb
>(+/- 0.2 kb) but would like to avoid the multiple extraction procedure 
>described in Maniatis.  My goal is to sequence the product so it must be
>relatively clean.  Anybody got an improvement on the Maniatis technique
>or must I haul out the phenol?
>Bob Karn
>KARN at BUTLERU.edu



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