D406 Zymo Genomic DNA Clean And Concentrator Kit-25 in USA
The D406 Zymo Genomic DNA Clean & Concentrator-25 (DCC) is a spin column 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 gDNA clean-up kit is also compatible with smaller DNAs (50 bp to 10 kb) from PCR, digestions, crude plasmid preparations, cDNA synthesis, etc.
Cleanse and concentrate D406 Zymo genomic DNA effortlessly with our Genomic DNA Clean Concentrator Kit (25 preps). Optimize your research with purified DNA for accurate downstream applications. Order now for reliable results!
|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||≥ 35 µl of DNA Elution Buffer|
|Purity||A260/A280 > 1.8, A260/A230 > 1.8|
|Sample Source||Enzymatic reactions or impure preparations containing genomic DNAs|
|Sample storage||Eluted DNA can be used immediately or stored at ≤ -20°C|
|Size Range||50 bp to 200 kb|
|Yield||Recovery of DNA ranges from 70 – 95%|
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.