Details
Specifications
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Features
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Specifications
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Main Functions
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Selectively recover DNA from PCR products and enzymatic reaction solution (Replace Beckmen or agencourt AmPure XP)
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Applications
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NGS, DNA library
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Purification technology
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Magnetic beads technology
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Process method
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Manual (centrifugation or vacuum)
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Sample type
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DNA products, restriction endonuclease systems, or other enzymatic reaction solutions
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Sample amount
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Appropriate
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Recovery
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80%
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Operation time
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≤50 minutes
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Principle
This product is based on the purification method of high binding magnetic particles. PCR amplicons mix with MagPure A3, 100bp and larger DNA binds to magnetic beads. Excess primes, nucleotides, salts and enzymes can be removed using a simple washing procedure and finally DNA was eluted by Elution Buffer or Water.
Technical Validation
MagPure A4 XP was evaluated using internal quality-control testing for DNA fragment size selection, microscale DNA marker recovery and background nucleic acid assessment. The tested A4XP batch was compared with a standard control batch across multiple bead-to-sample ratios.
In macro-scale DNA marker size selection testing, MagPure A4 XP showed ratio-dependent fragment recovery patterns from 0.6× to 1.8× bead volume. Agarose gel analysis showed no obvious difference between the tested batch and the control batch, supporting consistent size selection behavior across the tested ratios.
Microscale DNA marker recovery was further evaluated at 0.6×, 0.9×, 1.2× and 1.8× bead ratios. The tested batch showed average recovery rates of approximately 30.2%, 58.4%, 70.7% and 86.9%, respectively. Recovery at 0.9×, 1.2× and 1.8× was comparable to the control batch, while the lower recovery observed at 0.6× was attributed to small elution-volume variation under the 50 µL elution condition.
Background nucleic acid testing showed Qubit readings below the detectable range for the tested A4XP bead batch, indicating no detectable nucleic acid background under the tested conditions.
In addition, MagPure A4 XP was evaluated against AMPure XP in library preparation cleanup and size selection workflows using pooled cfDNA samples. In single size selection testing, the tested MagPure A4 XP batches produced mean library concentrations of approximately 7.99–8.32 ng/µL, compared with 6.35 ng/µL for AMPure XP under the tested conditions.
In double size selection testing, MagPure A4 XP batches produced mean library concentrations of approximately 3.15–3.72 ng/µL, comparable to 3.39 ng/µL for AMPure XP. Microscale 50 bp DNA marker recovery also showed comparable high recovery at 1.2× and 1.5× bead ratios, with MagPure A4 XP batches reaching approximately 93–97% recovery.
These results support the use of MagPure A4 XP for PCR product purification, library cleanup and NGS size selection workflows requiring consistent bead performance, controlled fragment recovery and AMPure XP-like workflow compatibility.
Kit Contents
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Contents
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BP-5
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BP-50
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BP-500
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MagPure A4 XP
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5 ml
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50 ml
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500 ml
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Storage and Stability
MagPure A4 XP should be stored at 2-8°C upon arrival and is stable up to 18 months under the condition. However, short-term storage (up to 4 weeks) at room temperature (15-25°C) does not affect its performance. — Shake the reagent well before use. It should appear homogenous and consistent in color.
DO NOT FREEZE.