Table 1 of Xiao, Mol Vis 2011; 17:2049-2055.


Table 1. Primers used to amplify genomic fragments of candidate genes.


Gene
name

Primer
ID


Primer sequence (5'-3')
Product
length
(bp)
Annealing
temperature
(°C)
CRYBB2 1F TTGGGGCCAGAGGGGAGTG    
  1R TGGGCTGGGGAGGGACTTTC 353 66
  2F AGGTCCCACGGCTGCTTAT    
  2R GGCTGCCAGACCCCAAAACT 421 64
  3F GTGGGTAAAGGCAGCATAGC    
  3R GGCAGAGAGAGGGAGTAGGG 378 68
  4F GGTGCACTGGGAAGAGAGTG    
  4R GAAGCCAGAGGTCAGCAGAG 397 60
  5F GAGGCTTCACCCTTCCTAGTG    
  5R GCAGACAAGTTGCAAGTCAC 389 69
CRYGD 1-2F GGGCCCCTTTTGTGCGGTTCT    
  1-2R GTGGGGAGCAAACTCTATTGA 643 65
  3F TGCTCGGTAATGAGGAGTTT    
  3R AAATCAGTGCCAGGAACACA 506 63
MAF 1aF GAGCGAGGGAGCACATTG    
  1aR CCGGTTCCTTTTTCACTTCA 352 60
  1bF AACTGGCAATGAGCAACTCC    
  1bR GTGGTGGTGGTGGTGGTAGT 548 60
  1cF CCGCACTACCACCACCAC    
  1cR CTGGTTCTTCTCCGACTCCA 432 60
  1dF AGCTGGTGACCATGTCTGTG    
  1dR AGAACTAGCAAGCCCACACC 407 53.5
  2F AAATCCTGAGTAAGTGCCATTCA    
  2R GTTGCATTCCGGGAAACTT 575 60
MIP 1F GACTGTCCACCCAGACAAGG    
  1R TCAGGGAGTCAGGGCAATAG 492 64~57
  2F TGAAGGAGCACTGTTAGGAGATG    
  2R AGAGGGATAGGGCAGAGTTGATT 500 64~57
  3F CCAGACAGGGCATCAGT    
  3R TGGTACAGCAGCCAACAC 373 64~57
  4F AAGGTGTGGGATAAAGGAGT    
  4R TTCTTCATCTAGGGGCTGGC 429 64~57
  SeqE1R AAGGCACGGAGCAGGGACATC