Hi,

I am preparing STE buffer for genotyping in the method following. I want the buffer to have a final pH of 8.

Tris - 100mM

EDTA- 5mM

SDS-0.2%

NaCl- 200mM

Is TRIZMA base is more suitable or Tris- hydrochloride more suitable for this preparation?

Can you suggest me any protocol for genotyping?

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