Nanosep Centrifugal Device, Nucleic Acid Binding, 24/Pk - ODNABC33
Pall's quality infrastructure extends from the process-scale filtration and separation systems it supports worldwide to its laboratory devices. Spin-column NAB devices isolate DNA and RNA through a bind, wash, and elute workflow. Quartz glass fiber drives bind-wash-elute purification under centrifugal force while capturing DNA and RNA by surface adsorption and increases binding surface area for higher capacity. For genomic, plasmid, and amplicon work, dual-layer silica folds purification into a simple spin.
Key Characteristics
- Compatible with guanidine salts and ethanol or isopropanol wash buffers
- Layered glass fiber increases binding surface area for higher capture yield
- Releases purified template under low-salt elution into a clean collection tube
- Dual-layer silica binds nucleic acids by surface adsorption under high salt
- Recovers DNA and RNA fragments from fifty to ten thousand base pairs
Isolating clean, concentrated nucleic acid from a crude lysate sets up every molecular assay you run. Reliable nucleic acid capture delivers purified template ready for your assay through a simple bind, wash, and elute spin. Request a quality certificate, lot documentation, or a blanket-order quote from the Tisch Scientific support team.
- Sterility
- Nonsterile
- Wettability
- Hydrophilic
- Nucleic Acid Recovery - Binds and elutes nucleic acids from fifty to ten thousand base pairs in a simple centrifugal workflow.
- Gel Extraction - Recovers DNA fragments excised from agarose gel slices for cloning and downstream molecular applications.
- Amplicon Cleanup - Recovers amplified DNA fragments from reaction mixtures before sequencing or library preparation workflows.
- RNA Isolation - Recovers RNA from lysed samples for reverse transcription, expression analysis, and downstream molecular work.
- DNA Purification - Captures and purifies genomic DNA from cell and tissue lysates for sequencing and amplification workflows.
- Plasmid Cleanup - Isolates plasmid DNA from bacterial lysates ahead of cloning, transfection, and restriction digestion steps.