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. 2011 Dec 2;6(12):e28357. doi: 10.1371/journal.pone.0028357

Table 1. Primers sequence, annealing temperatures and size of PCR products used to amplify and sequence exons of the G6PD gene.

Exons Primer name Sequence (5′-3′) Hybridization T° Size of PCR products
Exon 2 PCR_G6PD_Ex2_F TGAAGGCTGCCTAGGAGAGA 58°C 494 bp
PCR_G6PD_Ex2_R CAGGTAGAGCCGGGATGAT
Exons 3–4 PCR_G6PD_Ex3–4_F TGTCCCCAGCCACTTCTAA 58°C 400 bp
PCR_G6PD_Ex3–4_R GGAGAGGAGGAGAGCATCC
Exon 5 PCR_G6PD_Ex 5_F CGGGGACACTGACTTCTG 56°C 500 bp
PCR_G6PD_Ex 5_R ACGCTGCCACCTTGTGGT
Exons 6–7 PCR_G6PD_Ex 6–7_F ACACAAGGCACGGGAGGT 58°C 697 bp
PCR_G6PD_Ex 6–7_R GAGGAGCTCCCCCAAGATAG
Exon 8 PCR_G6PD_Ex 8_F CCCTTGAACCAGGTGAACAG 58°C 221 bp
PCR_G6PD_Ex 8_R TCAGTGCCTCGTCACAGATG
Exon 9 PCR_G6PD_Ex 9_F CCTGAGGGCTGCACATCT 58°C 363 bp
PCR_G6PD_Ex 9_R GTGCGTGAGTGTCTCAGTGG
Exons 10–11–12 PCR_G6PD_Ex 10–12_F TGAGACACTCACGCACTGGT 58°C 752 bp
PCR_G6PD_Ex 10–12_R TGAGGTAGCTCCACCCTCAC
Exon 13 PCR_G6PD_Ex 13_F TTATGGCAGGTGAGGAAAGG 58°C 848 bp
PCR_G6PD_Ex 13_R GAAGTGGGTCCTCAGGGAAG