MagSi-DNA beads are magnetic silica beads with a nanoporous surface optimal for nucleic acid binding. Due to the superparamagnetic properties and bead size of 3µm, the beads sediment very slowly and typically collects within 1-2 minutes in a magnetic field. This makes them applicable for both manual and automated/robotic DNA isolation.
The magnetic microparticles are intended as a solid phase extraction tool for custom buffer systems based on chaotropic and non-chaotropic binding principles. They can be used for developing your own nucleic acid isolation and extraction methods, such as:
MagSi-DNA beads reversibly bind DNA and other nucleic acids under sample- and buffer-specific conditions. A solution containing DNA (e.g. lysate) is combined with the beads and an application-specific binding buffer. After incubation, nucleic acids are bound to the silica surface. By applying a suitable magnet to the container (tube/deepwell microplate), the bead pellet is separated from the sample mixture. Unwanted components are further removed by washing steps in a selection of buffers. Finally, nucleic acids are released in a DNase/RNase-free water or buffer solution.
MagSi-DNA beads are available with a silica surface and with a carboxylated surface. The two surfaces differ in their optimal binding conditions. When developing a new application, it is recommended to try both types in parallel.
Please note: When separation speed is crucial and sufficient homogenization tools are available, 300nm beads may be more suitable due to their short separation time.
Cat# | Product | Surface | Volume |
MD01022 | MagSi-DNA 3.0 | Silica | 2ml |
MD03022 | MagSi-DNA 3.0 | Silica | 10ml |
MD01024 | MagSi-DNA 3.0 COOH | Carboxylated | 2ml |
MD03024 | MagSi-DNA 3.0 COOH | Carboxylated | 10ml |
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