Table 1 of Szaflik, Mol Vis 2008; 14:1713-1718.


Table 1. Primers for polymerase chain reaction amplification and sequencing of KRT3 and KRT12, their annealing temperature (Ta), and expected amplicon size.

Gene/exon Forward primer sequence (5’→ 3’) Reverse primer sequence (5’→ 3’) Ta (°C) Product size (bp)
KRT3
exon 1 TgCACAggTCTTCATTTCCCATCC TCCTCAACCCTggATATCTTCCCA 61 887
exon 2 AgTgTTgCCTgATgTTgCTTCCTg ACCATgCTTggAgAAggAAggTgA 61 439
exon 3 ATggAgggAgggAAgAgATgAACT ATTgCTCCAAAggCCTGAACTTgg 61 275
exon 4 gCTCTTTCTTgCTgCAgTTgTggT gCACCAgCCTCAAATCTggAAACA 60 238
exon 5 AgTgAACAAgCTCCCTCTgTgTTg TgAAACCTCCAgTggATCCCgTAA 60 235
exon 6 AAggTTTggTgggTgATgTTggAg ATTTgTggAgATACTgCCCTgTgg 61 345
exon 7 AATCCATTgCATgTCAggAAgggC TATCTGGCCCTTGGCCTATGACTT 60 354
exon 8 TgTTggTgATgTgCTTTgTgACgg AAgCCAATCACTTCCCTCTCCTCT 60 228
exon 9 ACAATAACATAgCAgCTggCCTgg AATACTCAgAggCCCggAgTgAAA 61 756
KRT12
exon 1a AgTgAACTTTTCAACTgCgA TgCCCgAgAgAATACCTAgA 61.5 450
exon 1b AggACTgggTgCTggTTAT CTgCAAgTACAgCTAAATTggA 62 447
exon 2 TAgggCTTCAATCTTgTgTgTgTCCC TTTATATCAATgAAggCAggACAgTAggAC 61.2 200
exon 3 CCCTCAACTgCTTTgCACTTggTT CTCCATACTTgTCCTgACTCCAgA 58.4 289
exon 4 CAgggCCCACgAAAgTCACAAT gTTCgCAggCCTTTCTgTgAATgT 58.3 272
exon 5 ACATTCACAgAAAggCCTgCgAAC TggAAgTCCAAAggATgCTACgTC 58.4 235
exon 6 gCTCgTgCgCAAACAgACgT CCCAggCATATCTTTACTAgA 60 490
exon 7 AgCCACCTgAACCACCTACTCTAA AgCTATgAggTTACAggCATgAgC 63 469
exon 8 gCCTACATTAAACAACCAgTgTTgg CAAgCAATCATCTTgCCTCTCAgC 61 684