The purity of your salting-out approach is one of its vital downsides; whilst a enough produce may be reached, the standard obtained may not be satisfactory. To evaluate just how much history bacterial DNA was present from the samples, we performed qPCR of bacterial 16S rRNA genes and calculated the https://www.facebook.com/NewTechFind/posts/pfbid02CsD3AaVcSkRwFf5Xd4E45XYBXLEW11uKWALk2WS43BHgfobUpcD4tRuHLPRx9NCvl