Catalog No. LM801002

SEQQX® DNA Selection Beads

SPRI-based magnetic beads for DNA fragment size selection and purification during NGS library preparation, with a two-step selection protocol and adjustable bead-to-sample ratios.

SPRI magnetic beads
Two-step size selection
NGS library preparation
RUO

Product overview

SEQQX® DNA Selection Beads, catalog no. LM801002, combine solid phase reverse immobilization (SPRI) with an optimized buffer system for DNA fragment selection and purification during NGS library preparation. The handbook describes compatibility with DNA and RNA library preparation kits from multiple manufacturers and a workflow following the AMPure XP bead protocol. Two successive bead additions enable selection of defined DNA fragment-size ranges.

NGS library preparation

Select and purify DNA fragments within DNA or RNA library preparation workflows.

Adjustable size selection

Six reference ratio pairs target fragment ranges from 250–350 bp to 800–1000 bp.

Magnetic separation

The two-step protocol uses a magnetic stand, two 80% ethanol washes and elution in at least 20 µL of water.

Specifications

ParameterValue
TechnologySPRI magnetic-bead DNA size selection and purification
MethodTwo-step selection; magnetic stand required
Starting sample volumeAt least 100 µL; adjust with ultrapure water if needed
EquilibrationAt least 30 min at room temperature before use
250–350 bp selectionFirst-round ratio 0.80×; second-round addition 0.20×
320–420 bp selectionFirst-round ratio 0.70×; second-round addition 0.20×
450–550 bp selectionFirst-round ratio 0.60×; second-round addition 0.20×
550–700 bp selectionFirst-round ratio 0.55×; second-round addition 0.15×
700–900 bp selectionFirst-round ratio 0.50×; second-round addition 0.15×
800–1000 bp selectionFirst-round ratio 0.45×; second-round addition 0.15×
Ratio basisBoth bead additions are calculated from the original DNA sample volume
WashingTwo washes, each 200 µL freshly prepared 80% ethanol for 30 s
ElutionAt least 20 µL ddH₂O; 5 min at room temperature
Storage and shelf life2–8°C; 18 months
Intended useResearch use only

Pack sizes & ordering

Catalog No.Pack sizeFormat
LM8010021 mLMagnetic-bead suspension
LM8010025 mLMagnetic-bead suspension
LM80100210 mLMagnetic-bead suspension
LM80100260 mLMagnetic-bead suspension
LM801002450 mLMagnetic-bead suspension

Specify the required volume when ordering. Bead consumption depends on the initial sample volume and the selected ratio pair. Source: LM801002_SEQQX_DNA_Selection_Beads_12601.pdf, pp. 2–4.

Performance & validation

The handbook demonstrates two-step selection using ultrasonicated calf thymus DNA spanning 100–1000 bp, with results assessed by Agilent 2100 Bioanalyzer. It describes recovery and library-size distribution as closely matching AMPure XP beads, without providing a numerical recovery percentage. Source: LM801002 handbook, pp. 2–4.

Six reference size windows

Ratio pairs from 0.80×/0.20× to 0.45×/0.15× correspond to six reference fragment-size ranges.

Electropherogram evidence

Agilent 2100 High Sensitivity DNA Chip analysis is shown for fragmented calf thymus DNA dissolved in water.

Selection conditions

Use at least 100 µL starting DNA solution, equilibrate beads and avoid over-drying to support consistent selection.


SEQQX LM801002 Performance2
SEQQX LM801002 Performance1

Product documents

Product FAQs

How are the bead volumes calculated?

Both additions use the original DNA sample volume. For 100 µL at 0.80×/0.20×, add 80 µL first, then 20 µL to the transferred supernatant.

Which fraction is retained?

Keep the supernatant after the first selection. After the second selection, keep the beads, wash and elute the DNA.

What if the sample is below 100 µL?

Add ultrapure water to at least 100 µL before size selection.

What preparation is required?

Equilibrate beads for at least 30 min at room temperature, mix thoroughly and prepare fresh 80% ethanol. Avoid over-drying after washing.

How should the product be stored?

Store at 2–8°C. Shelf life is 18 months. Research use only.

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