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Table 4 Combinations of GenSolve, Qiagen and NucleoSpin protocols for DNA extraction from DBS: GQ versus NN and Nn methods

From: Optimized DNA extraction from neonatal dried blood spots: application in methylome profiling

      

65°C, 65 min

  
 

Sample code

DNA (ng/μl)

DNA (ng)

260/280

260/230

260/280

260/230

Protocol

 

NCS 1a

25.3

1062

1.84

1.15

1.88

1.18

GQ

NCS 1b

40.0

1802

1.82

1.84

1.90

1.90

NN

NCS 2a

28.8

1209

1.87

1.27

1.89

1.33

GQ

NCS 2b

47.3

2127

1.89

2.00

1.90

1.91

NN

NCS 3a

15.2

638

2.02

1.09

1.93

1.15

GQ

NCS 3b

27.6

1271

1.82

1.59

1.91

1.61

NN

NCS 4-4a

23.0

987

1.93

0.93

1.96

1.03

GQ

NCS 4-4b

30.0

1348

1.85

1.72

1.90

1.81

NN

NCS 4-5a

33.4

1435

1.82

1.01

1.83

1.02

GQ

NCS 4-5b

35.4

1593

1.98

1.94

1.87

1.76

NN

NCS 4-6a

19.9

856

2.01

1.14

1.97

1.10

GQ

NCS 4-6b

33.9

1525

1.93

1.85

1.89

1.82

NN

Precipitation buffer in NN changed to ethanol, leading to protocol Nn

NCS 4-7a

18.0

774

1.76

0.87

1.86

0.84

GQ

NCS 4-7b

25.7

1155

1.93

1.37

1.81

1.35

Nn

NCS 4-8a

14.7

617

1.99

0.90

1.94

0.91

GQ

NCS 4-8b

24.6

1105

1.92

1.33

1.85

1.42

Nn

NCS 4-9a

26.1

1121

1.90

1.20

1.94

1.26

GQ

NCS 4-9b

39.0

1754

1.95

1.89

1.88

1.77

Nn

  1. Two punches, each having 9 mm diameter, were analyzed per DBS. Punches labeled “a” were tested with GQ while their matched pairs, labeled “b”, were tested with NN. When the DNA precipitation buffer in NN was changed to ethanol, the resultant protocol was termed Nn. Average eluate volumes by GQ and NN/Nn were 42 μl and 45 μl, respectively. Data represent averages of 2–4 readings per sample.