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Table 2 primer sequences for the PCR amplification at the entire coding regions and exon/intron boundaries of the NPC1 gene

From: Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

Fragment

Exon

Forward(5’-3’)

Reverse(5’-3’)

Product size(bp)

Tm (°C)

1

E1

AGCCGACGACGCCTTCTTCCTT

ACAAGTGAGGAACCTCCGAGCTC

383

61.6

2

E2

GAAGTTTCTGTGATTGTACTTGAGT

TCCACCTCCACCCTGCAATAACAT

310

61.7

3

E3

GTGTCTTAGTTCACTGAGGAATGTTG

GAAAGCTGAGCATTACCAGTTCACA

253

64.3

4

E4

TGGACACAATAAATGCAGAAAGTAAT

TGACAGGACAACTAAAAGGAACAAT

475

63.4

5

E5

AGCATGGTGCATATGGAGTTCGTG

CAAGCACTGGTGAGCCACTGTGC

369

63

6

E6

GTATTTCAGTGGGCTTTTCTTTGAGT

CATGGAGGTATTTGTTTCTTGTCCTA

475

62.5

7

E7

ACCTCACTGTGATGAAGTCCACTA

CATGACAGACAGCATCATCTGAAC

178

60.7

8

E8

TGATTCCTGCCATGAGATAGCAACT

CCCATCTAGCAGTAGTCAACATGTA

556

60.8

9

E9

ATGTGACGTGTTTCTGGGTTTGC

GTCTTGTTGTTTGCTCACCTCTG

384

62.2

10

E10

AGGTGAGTGCTGAGCTGTATTA

AGGAGATACTATTCTGGGATTCA

403

62.4

11

E11

AGATACAGTCCATAGCTCCAGTGAG

TAAGTGCTTGCTGCAAGTGTCTAGC

288

61.1

12

E12

TCGTGAAAGTTAGGGAGAAGTTT

GGCAACAGAAACGTTACATACAA

312

63.4

13

E13

TTTAGTAACAAGTGGGACAGACAAC

AGGTCACACTCACGAATGCGGAG

339

64.3

14

E14

AGTCCCCCACCGAAGTTTAT

AGCCAGCTCCTTCTTTCTCC

233

61.8

15

E15-16

GCTGTAAACAGAAGTGACGCAGA

CTGGCTTCTTAGAAGGCATGTGAT

480

62.2

16

E17

CCTGTACTCCCTATTAGCCTGTCAT

ACTTGCTTGAAACACCTACGTGCATG

322

63.2

17

E18

TGCTTAGTTACTATCAGAGTGTTCAC

CCTCCTCCGCTGCTTCTGAAGTA

291

61

18

E19

CTGTGGAGCAGGTCAGTAACCCT

GTATAAACTGAGGCACGATGCAAATG

245

62

19

E20

CTTCTAACAGTCCTCCCTGCA

CTGTCTTAGCCCAGTCCTCTC

247

64.3

20

E21

TGCTTAGCCTCAAGTGCTCAGAT

ACCCAGTGTAGGCCCTTTGCTG

337

63.7

21

E22

CATGAGAGGTCAAGTGAGTTG

ATGCTCGCTCCCTCTATG

295

62.2

22

E23

CAGGGTGCCCTGGGTAATTAGCA

GATCCAGACTCTTCAGTCACTGAG

292

61.6

23

E24

TTCAATTACAGGTTGGTAAAAGTGGTT

CTTGAAAAGAATGCCTCAGGATAGA

297

63.1

24

E25

TTCCAAAGTGGGATTACAGGCGTG

GACCGACCCTTAGACACAGTTCAG

221

64.3