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The system is ideal for low-copy number and hard-to-isolate plasmids
this buffer is the final column wash to prepare for pure DNA to be recovered and eluted
Control DNA and primers are included to monitor the success of the assay
non-methylated DNA
Eluted DNA is suitable for PCR
RNase A DNA Hydroxymethylation The system is ideal forRNase A is a highly active and stable enzyme that specifically digests RNA across a wide range of buffer conditions and temperatures. It is purified from bovine pancreas and is free from DNase and protease contamination. The lyophilized enzyme can be reconstituted to a concentration of up to 10 mg ml. RNase A has been rigorously tested for plasmid and genomic DNA purifications, ensuring its reliability and efficiency.
US$ 29700.00
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