AcuGenix™ NGS DNA Clean Beads

AcuGenix™ NGS DNA Purification magnetic beads

Superparamagnetic beads empower standardized and high-recovery nucleic acid purification and fragment screening

This product takes high-performance superparamagnetic beads as its core and is equipped with an optimized buffer system, which can achieve efficient and repeatable purification and screening of nucleic acid fragments. By adjusting the ratio of magnetic beads to samples, target fragments can be selectively combined to precisely recover nucleic acids within a specified size range. The operation process is completely consistent with the industry gold standard AMPure XP magnetic beads and can directly replace the purification reagents in the existing NGS library construction process without the need to re-optimize the experimental plan. This product supports both manual operation and is compatible with various mainstream automated liquid handling workstations, meeting the experimental requirements of different fluxes.

1. Precise fragment screening
The controllable recovery of nucleic acids within the target size range is achieved by adjusting the proportion of magnetic beads, adapting to the fragment selection requirements of different NGS applications.

2. Compatible with common industry processes:
The operation process is exactly the same as that of AMPure XP. Replacing the existing reagents does not require adjusting the experimental plan, significantly reducing the cost of methodological validation.

3. Compatibility with broad-spectrum library construction kits
Compatible with DNA and RNA library construction kits from mainstream manufacturers, and adaptable to various mainstream NGS library construction processes.

4. Dual compatibility of manual and automatic:
It supports both desktop manual operation and is compatible with various mainstream automated liquid handling workstations, covering throughput requirements ranging from routine scientific research to high-throughput detection.

5. Excellent batch stability
Strict batch quality control ensures the consistency and repeatability of purification results and reduces the risk of experimental failure.

Purification at each step of the NGS library (after fragmentation, ligation, and amplification).

2. Fragment screening for whole genome sequencing (WGS), whole exome sequencing (WES), RNA sequencing, and targeted sequencing libraries.

3. Purification of PCR products, enzymatic reaction products and low starting amount nucleic acid samples.