Quick, high-throughput (96-well) recovery of large-sized DNA from any enzymatic reaction or impure preparation without messy precipitations
UniqueUnique spin column for low volume elution of ultra-pure, high-yield DNA. spin column for low volume elution of ultra-pure, high-yield DNA
Eluted DNA is ideal for PCR, endonuclease digestion, sequencing, etc.
Description
The ZR-96 Genomic DNA Clean & Concentrator (DCC) is a 96-well gDNA clean up kit that provides quick (5 minute) recovery of ultra-pure, large-sized DNA (e.g., genomic, mitochondrial, plasmid (BAC/PAC), viral, phage, (wga) DNA, etc.) from any enzymatic reaction or impure preparation (e.g., Proteinase K digestion). There is no need for organic denaturants, chloroform, or messy precipitations: simply add the specially formulated ChIP DNA Binding Buffer to a sample and then transfer the mixture to the supplied Zymo-Spin Column. Eluted DNA is suitable for sequencing, PCR, endonuclease digestion, and other enzymatic procedures. This 96-well gDNA clean up kit is also compatible with smaller DNAs (50 bp to 10 kb) from PCR, digestions, crude plasmid preparations, cDNA synthesis, etc.
Technical Specifications
Applicable For
Eluted DNA is ideal for ligation, sequencing, labeling, PCR, microarray, transfection, transformation, restriction digestion procedures, and any other sensitive downstream application
Elution Volume
≥ 15 µl of DNA Elution Buffer
Equipment
Centrifuge w/ microplate carriers
Purity
A260/A280 > 1.8, A260/A230 > 1.8
Sample Source
Enzymatic reactions or impure preparations containing genomic DNA
Sample storage
Eluted DNA can be used immediately or stored at ≤ -20°C
Size Range
> 50 bp and up to 200 kb
Yield
Up to 5 µg DNA. Recovery of DNA ranges from 70 – 95%
Product FAQ
Q1: What is the lower limit and minimal amount of DNA that can be recovered?
Picogram levels of DNA can be recovered. The limitation is based on sensitivity of detection method.
Q2: How to process naked DNA stored in DNA/RNA Shield?
Use the standard protocol (add 2 or 5 volumes of DNA binding buffer depending on DNA size).
Q3: What to do if ethanol addition to the DNA Wash Buffer was omitted?
The DNA will be eluted off the column. Rebind samples using the appropriate amount of DNA Binding Buffer and wash the column with the properly prepared wash buffer.
Q4: What happens if more DNA was loaded on the columns than the stated maximum binding capacity?
Oversaturation of the column can result in total DNA loss due to clogging of silica matrix.
Q5: How many times can columns be reloaded?
We recommend no more than 5 times as binding efficiency might decrease.
Q6: What is the minimum input volume of DNA sample?
Working with volumes below 50 µl can result in decreased recovery. We recommend raising the starting volume to 100 µl with water to ensure optimal binding conditions.
