Is it necessary to perform this procedure? It may incur additional expenses and effort or just the QC step prior to quantification or cloning.
I've done DGGE and never cleaned my pcr reactions before do DGGE electrophoresis.
I agree with Ana Machado.
Other way is try improve PCR reaction, adding BSA and DMSO or changing some conditions of PCR reactions. I guess that add BSA and DMSO you can improve your reaction getting a band only.
If you have a single band in your agarose gel then there is no need to clean up your PCR products before running DGGE.
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Is there any formula or specific program?
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