Magnetic Beads for DNA Normalization
Bead-based DNA Normalization
- Consistent DNA quantity normalization of various sources in excellent dynamic range
- Easy and efficient protocol – no centrifugation, no filtering
- No more fluorescent quantitation needed
- Cost and Time Saving
- Removal of unwanted components and impurities
- Elution in as low as 10-20 µl without yield loss
- Ideal for High Throughput Sample Processing

DNA Normalization Magnetic Beads were developed to normalize NGS libraries, PCR fragments, sheared genomic DNA, and genomic DNA based on BioDynami´s magnetic bead technology.
During bead-based normalization, any DNA samples of varying concentrations are bound to BioDynami´s magnetic DNA normalization beads characterized by a defined limited DNA binding capacity. Bound DNAs are separated from excess unbound DNA and are subsequently eluted off the beads at approximately the same concentration for each sample.
Specifications of DNA Normalization Magnetic Beads
| Cat.# | 40071/40072 | 40073 | 40075 | 40077 | 40079 |
| NGS Library Input | √ | √ | √ | √ | √ |
| PCR Input | √ | √ | √ | √ | √ |
| Sheared gDNA Input | √ | √ | √ | √ | √ |
| gDNA Input | √ | ||||
| Input Range | NGS, PCR: 300-2000ng
gDNA: 500-5000ng |
150-1200 ng | 50-300 ng | 15-100 ng | 5-30 ng |
| Normalized Range | NGS, PCR: 100-180ng
gDNA: 150-270ng |
100-320 ng | 25-60 ng | 5-15 ng | 1.5 -4.5 ng |
| Elution Volume | >20 μl | >10 μl | >10 μl | >10 μl | >10 μl |
BioDynami kits 40072S and 40072L additionally include special recovery beads for the recovery of unbound excess DNA during DNA normalization.
Traditional fluorescent methods of normalization require the setup of a standard curve from known concentrations, compare with samples, aliquot adjusted volume for each sample, and add adjusted volume of elution buffer to match the total volume for each sample. The whole procedure needs extensive efforts, expensive reagents, and has a long processing time. In contrast, the beads-based protocol is simple, fast, centrifugation free, and filtration free. Additional DNA quantification and dilution is not necessary after normalization with magnetic beads. Labor, time, and reagents are all saved by the use of DNA normalization beads.
Applications of BioDynami´s Magnetic DNA Normalization Beads:
NGS Library Normalization
Magnetic bead-based NGS library normalization provides significant cost and time savings especially when processing many samples.

Normalization of NGS Libraries: Input NGS library amounts and normalized NGS library amounts
This efficient, time-saving alternative bypasses time-consuming and costly library quantitation measurements using fluorescence and/or fragment analyzer instruments. Moreover, manual pipetting steps including dilutions before loading NGS libraries onto the sequencer are no longer necessary.
Normalization of Genomic DNA and of PCR Products
Varying amounts of genomic DNA (including sheared genomic DNA fragments in different samples) as well as of PCR Products can easily and conveniently be normalized to uniform DNA concentrations by BioDynami´s Magnetic DNA Normalization Beads.

Normalization of Genomic DNA: Input Genomic DNA amounts and normalized Genomic DNA amounts

Normalization of PCR Products: Input PCR Products DNA amounts and normalized PCR Products DNA amounts
BioDynami´s unique Magnetic Beads Technology
BioDynami´s magnetic beads are based on SPRI (Solid Phase Reversible Immobilization) and consist of paramagnetic particles coated with carboxyl groups that reversibly bind nucleic acids or paramagnetic particles coated with a proprietary chemistry enabling binding to small nucleic acids -technology background information can be found in the publication from Ribeiro et al. (ACS Omega, Jan 21, 2026)
More BioDynami Magnetic Beads-based Products
NGS Library Size Selection/DNA Size Selection Kits
NGS Library and DNA/RNA Purification and Concentration
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