PCR Purification Beads
Purification of PCR fragments >80 bp
Removal of primers <30 nt
Manual/automated processing
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Description:
The magnetic beads for plasmid purification from the American company BioDynami combine BioDynami's patented chemistry with the unique properties of SPRI beads (Solid Phase Reversible Immobilization). These beads effectively eliminate RNA contamination from isolated plasmid DNA samples. Additionally, they remove undesirable components such as salts, dNTPs, proteins, enzymes, and other impurities. The purified plasmid DNA obtained using this method is ideal for downstream applications such as enzymatic digestion, transformation, transfection, molecular cloning, and more. These beads provide an effective and cost-efficient tool for removing bacterial RNA during routine plasmid purification.
The image visualizes a comparison of samples before and after using magnetic beads for plasmid DNA purification. The left panel shows significant RNA contamination in the unpurified sample (-), while the right panel demonstrates effective RNA removal after purification (+). The use of magnetic beads results in clean and high-quality DNA, ready for further analysis.

Workflow:
First, the plasmid DNA is mixed with magnetic beads that specifically bind to the DNA, while RNA and other impurities remain in the solution. The beads with bound DNA are then separated from the rest of the solution using a magnet, effectively removing RNA and impurities. Next, the beads are washed with a wash buffer to remove any remaining contaminants. Finally, the purified plasmid DNA is eluted from the beads, resulting in highly purified plasmid DNA.

Features:
Package size:
40 reactions (Cat. No. 40059S)
200 reactions (Cat. No. 40059L)
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Purification of PCR fragments >80 bp
Removal of primers <30 nt
Manual/automated processing
DNA isolation from 100 bases
RNA isolation from 200 bases
Elution volume from 10 µl
purification of short DNA/RNA fragments
removal of impurities
for manual/automated procedure
DNA and RNA concentrator
Binding capacity: 10 µg DNA per prep
Removal of unwanted components
dynamic range
without fluorescent quantification
no centrifugation and filtration
with recovery beads
miRNA purification
Efficiency up to 80%
Removal of tRNA, 5S RNA
dynamic range
without fluorescent quantification
no centrifugation and filtration
without recovery beads
Purification of tRNA and oligos (>70 nt)
Removal of RNA/DNA contamination
Efficiency approximately 83%
plasmid purification
removal of RNA
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