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Table 2 Experiment tested

From: An SPRI beads-based DNA purification strategy for flexibility and cost-effectiveness

Test component

Buffer composition

Work condition

Vol.beads/Vol.DNA

Separating time (min)

Incubated temperature

Incubated time (min)

PEG 8000

16.3% PEG 8000, 10 mg/ml beads, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

18% PEG 8000, 10 mg/ml beads, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

20% PEG 8000, 10 mg/ml beads, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

21.4% PEG 8000, 10 mg/ml beads, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

22.6% PEG 8000, 10 mg/ml beads, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

Beads (SPION particles)

10 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

5 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

2.5 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

1.25 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

0.675 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

Separating time

1.25 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

5

RT

10

1.25 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

2

RT

10

1.25 mg/ml beads, 20% PEG 8000, 2 M NaCl, 16.3 mM MgCl2

1.2×

1

RT

10

Incubated temperature

1.25 mg/ml beads, 10% PEG 8000, 1.25 M NaCl, 10 mM MgCl2

1.2×

5

28 °C

10

1.25 mg/ml beads, 10% PEG 8000, 1.25 M NaCl, 10 mM MgCl2

1.2×

5

25 °C

10

1.25 mg/ml beads, 10% PEG 8000, 1.25 M NaCl, 10 mM MgCl2

1.2×

5

18 °C

10