BamHI Methylation including good multiplex amplification performance

including good multiplex amplification performance

and offers high success rates and faster processing

adapter-ligated NGS libraries

allowing the reaction to be set up simply by adding the SNP-specific primers and DNA template

5 μg of fully 5-hydroxymethylated 1095bp PCR fragment from digestion by MunI within 1 hour at 37°C in a 50 μL volume of the recommended reaction buffer

BamHI Methylation including good multiplex amplification performanceRecognition site: 5' G G A T C C 3' 3' C C T A G G 5' Product Description The BamH restriction endonuclease recognizes the G^GATCC site and achieves optimal cutting efficiency within 515 minutes at 37C using the universal buffer. GDSBio restriction endonucleases exhibit 100% activity in both Digest and Green reaction buffers. The universal Digest buffer allows for rapid single enzyme, double enzyme, or multiple enzyme digestion of DNA within 515