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Table 3 Primers used for mutation search and gene expression analyses

From: Genetic mapping of high caries experience on human chromosome 13

Primers used for mutation search

Primer

Primer sequences (5′–3′)

Amplicon size (base pairs)

Thermal cycling condition

Forward

CAGCTTTATCGCCAGAGTCC

350

94°C 5 min→ 35×[94°C 30 sec, 56°C 30 sec, 72°C 30 sec]→72°C 5 min

Reverse

CCTCTTCCTCACCATCACCT

Forward

AAGAAGGTGGGGAGGAAGAG

550

94°C 5 min→ 35×[94°C 30 sec, 53°C 30 sec, 72°C 30 sec]→72°C 5 min

Reverse

GGTCATCCGAGATCATTAAAAA

Forward

TTTTTATACATATTGTTAGGGTCAGC

500

94°C 5 min→ 35×[94°C 30 sec, 53°C 30 sec, 72°C 30 sec]→72°C 5 min

Reverse

CAGTTTGTTTACCATCTCAAACACTT

Primers used for quantitative real-time polymerase chain reaction analysis

Target Gene

Primer

Primer sequences (5′–3′)

Amplicon size

Thermal cycling condition

   

(base pairs)

 

GATA1

Forward

TACTCAGTGCACCAACTGCC

114

50°C 2 min, 95°C 10 min→ 40×[95°C 15 sec, 60°C 1 min]→ 95°C 15 sec, 60°C 30 sec, 95°C 15 sec

Reverse

CGGTTCACCTGGTGTAGCTT

GR

Forward

AAGGGTTTGCTTTCACCCCA

138

Reverse

AAGCGTGTTGCAATTTCCCC

GATA3

Forward

GAGATGGCACGGGACACTAC

102

Reverse

CTGCAGACAGCCTTCGCTT

IL4

Forward

TCTTCCTGCTAGCATGTGCC

113

Reverse

GGTGCACAGAGTCTTCTGCT

IL5

Forward

AGCCAATGAGACTCTGAGGAT

116

Reverse

CAGTACCCCCTTGCACAGTT

IL13

Forward

ATGCATCCGCTCCTCAATCC

78

Reverse

AGTGAGAGCATGACCGTGG

GAPDH

Forward

ACCACAGTCCATGCCATCAC

452

 

Reverse

TCCACCACCCTGTTGCTGTA