I starting the DNA conversion with sodium bisufite in some concentration
but, after finish in the step of purification i found that the
disulfite converted DNA have the higher concentration than the starting DNA ~1000 ng
How could i solve the error rate in this problem? and
what are the factors the leading to this problem?
problems of purification
Started by Rainbowz, May 03 2011 10:36 PM
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