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| • | Quick (5 minute) clean-up of large-sized DNA from any enzymatic reaction or impure preparation without messy precipitations. |
| • | Unique spin column for low volume (≥ 10 µl) elution of ultra-pure, high-yield DNA. |
| • | Eluted DNA is ideal for PCR, endonuclease digestion, sequencing, etc. |
| Product | Catalog No. | Size | Price | Store |
|---|---|---|---|---|
| Genomic DNA Clean & Concentrator™ | D4010 | 25 Preps. | $ | |
| D4011 | 100 Preps. | $ | ||
| Components Available | ||||
| • | Format: Spin Column (capped) |
| • | Sample Sources: DNA from impure preparations of genomic DNA (e.g., Proteinase K digestions), plasmid DNA (including BAC), viral DNA, and whole genome amplified (wga) DNA.
Can also be used for the purification of lower molecular weight DNA (50 bp to 10 kb) from PCR, endonuclease digestion, post-RT cDNA synthesis, etc. |
| • | DNA Size Limits: Capable of purifying small DNA fragments >50 bp and large sized DNAs >200 kb. |
| • | DNA Recovery: Typically, up to 10 μg total DNA per column can be eluted with ≥10 μl water. Recovery of DNA ranges from 70 to 95%. |
| • | DNA Purity: Ultra-pure (A(260/280) ≥ 1.8) high molecular weight DNA is eluted in water and is especially well suited for PCR, sequencing, endonuclease digestion, etc. |
| • | Detergent Tolerance: ≤5% Triton X-100, ≤5% Tween-20, ≤5% Sarkosyl, ≤1% SDS |
| • | Equipment Needed: Microcentrifuge |
The Genomic DNA Clean & Concentrator™ (DCC™) is for the 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. The product is also compatible with smaller DNAs (50 bp to 10 kb) from PCR, digestions, crude plasmid preparations, cDNA synthesis, etc.
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Phage DNA Recovery. λ DNA (48.5 kb) is effectively recovered from 10-fold concentrations of starting material using the Genomic DCC™.
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High molecular weight DNA is efficiently purified using the Genomic DCC™. Porcine gDNA (~35-50 kb), T4 phage DNA (170 kb), and λ DNA (48.5 kb) were purified (in duplicate) from input material using the Genomic DCC™. Eluted DNAs were analyzed in a 0.8% (w/v) TAE/agarose/EtBr gel (shown above). The size marker “M” is a 1 kb ladder (Zymo Research).
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