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Hi Tim, thanks for your answer!
I will try tissue protocol then. Another question, I was reading some papers and they recommend pH 6 – 7 for silica DNA adsortion, could you explain why your pH lysis buffer is 7,6 – 8?
Best wishes.
Hello!
I was reading your protocol of gDNA extraction with beads and a got confused with ratio mentioned 2:3:4. How is it used with blood sample and without TE buffer at beggining? It’s 140ul of blood and 20ul magnetic bead?
Best regards.
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