DNA binding, wash and elution steps can be done using a vacuum manifold or by centrifugation.
3. After washing off the contaminants, the purified DNA is eluted by a low salt elution buffer or water.
2. And then DNA in chaotropic salt is bound to the glass fiber matrix of the plate.
1. The method uses proteinase K and a chaotropic salt, guanidine hydrochloride to lyse cells and degrade protein.
Introduction | |
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Introduction Format: 96-Well plates Sample:Blood, animal tissues, mouse tails, culture cells, swabs and other body fluids |