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Overview
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DNA purification procedure utilizes spin minicolumns with membranes which efficiently and selectively bind nucleic acids. First, CB Buffer is added to DNA sample. It causes proteins to degrade and enables DNA to bind with the column’s membrane. The binding buffer contains a color indicator, that facilitates an easy monitoring of the solution’s pH for optimal DNA binding. The two-step washing stage efficiently removes impurities and enzyme inhibitors. Purified DNA is eluted using either a low ionic strength buffer (Elution Buffer) or water (pH 7.0-9.0) and may be used directly in all downstream applications such as PCR, qPCR, DNA sequencing, enzymatic restriction, DNA ligation, etc. or stored until ready to use.
PRODUCT SPECIFICATIONS
SAMPLE MATERIAL
up to 200 μl of DNA sample
YIELD
60-99% – depending on DNA fragment length
DNA FRAGMENT LENGTH
50 bp – ~20 kbp
genomic and plasmid DNA, however the efficiency will be decreased
BINDING CAPACITY
approx. 40 μg DNA
TIME REQUIRED
10 min for 6 PCR purifications
DNA PURITY
A260/280 ratio = 1.7-1.9Please contact us at for specific academic pricing.
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- Properties
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Overview