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 |
Quality Control The quality of ATP Gel/PCR fragments Extraction Kit is tested on a lot-to-lot basis. The efficiency of DNA recovery is tested by isolation of DNA fragment of various sizes from either aqueous solution or agarose. The purified DNA is checked by agarose gel ...
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Quality Control The quality of 96-Well Gel/PCR DNA Extraction Kit is tested on a lot-to-lot basis. The efficiency of DNA recovery is tested by isolation of DNA fragments of various sizes. The purified DNA is checked by agarose gel analysis. The entire procedure can be completed ...
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2. ATP TM provide genomic DNA extraction protocols for smaller sample quantity. If larger sample quantity is required, user can scale up the buffer volume of the protocols proportionally. Introduction 1. ATP TM provide RBC Lysis Buffer to remove non-nucleated red blood cells ...
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