Table 1.
Exon # | Forward primer (5’-3’) | Reverse primer (5’- 3’) |
---|---|---|
1 | CGCTCCTCTCTGAGACAGAC | TTTTATAGAACATGCAACATTATCC |
2.1 | AATGAGTTTGGTTGAGGCAG | ATATCCAGCAGGGCAGATG |
2.2 | CAGTGGGACAATCTGTGAAAC | AATGTCACCTCTGCTTCTGC |
3 | GCTAAATTATGAACACTTTGCTAAAAC | GGTAAAATAGTTCATGGTCAGGG |
4 | CATGGGTCTTGGGTTGATAG | TTCATTTCATTTGCTATAAGCG |
5 | AACCTCCTTTTAGGCAAATG | GGTTAAAGCCATGGTCTGC |
6.1 | GAGCTATTCATGCACTTCTGC | GCCTCTGCAAATATTACCTCC |
6.2 | GAAGCTGGAGCTGCTAAGTG | TTTGCTGTTTCTGCTCTGC |
7.1 | TCCATCCCTTCTGTCTTTTG | TCCTAGGTTTTGTGAAGACTGA |
7.2 | TGGTGGGTCAGTAACATCATC | GCAATGCTGACTCCAAACTC |
8 | CAGATATGTGGTTTCACCGTC | TCTGTGTTTGCTCTTGGAAC |
9.1 | AAAAGCAACTAGCACAGTATGTAAC | AACTGCAAACAGCCAGTGAC |
9.2 | TGTGGGAGACAGAGCTATTGA | CTTGAGGAGAGAGCTTTCCAA |
10 | CTTTTCTTGAATGAGATGAACAAG | GAACTTTGAGTAATCCCATCATTC |
11 | GCTGTTCCAGAGAGATAAGGC | CTCAACAACTGGCTCGTCAT |
12 | TTCCTGAGTAGTTCCATTGTCC | CCCAGTTGCAGATTAACATTG |
List of primer used for Sanger sequencing of CRB1 gene. Multiple overlapping primers were used to amplify and sequence exons 2, 6, 7, and 9.