Table 1 of Peng, Mol Vis 2009; 15:810-814.


Table 1. Primers and PCR conditions used to amplify genomic segments of GPR143.


Primer
name


Primer sequence (5′-3′)
Annealing
temperature
(°C)
Product
size
(bp)
Exon 1-F AACCTTCCCAACCTTTCTGC 69 698
1-R CCTCTCGTCCTCACTCCATC

Exon 2-F CAGTGAGCAGGGTTTTTACCA 66 537
2-R AACAGACTCCCAGGGTTTGC

Exon 3-F GTCTACCCTGCCGTCTCAAG 66 334
3-R TGAGCTGCTGTGGATGTTTC

Exon 4-F CTCAGCAGCACGAGGAAACT 67 465
4-R ACAAACGAGAAAGGCAGAGC

Exon 5-F CTTAGGGGTCCTCCCATTTC 65 575
5-R TGGCACTGAGCTAACAAACG

Exon 6-F ATCCCCATGGTTGCATAAGA 64 738
6-R CACATGGTTGGGACATTTCA

Exon 7-F GCACCTGGCCCTCTTAGTTT 67 436
7-R GAGGCCAAGACAGAGGATTG

Exon 8-F TTCAGGCACCCTTGAAGGTA 66 539
8-R CCGGGACAAAGAATCCTCTA

Exon 9-F GGCTTGTGTCATCCGTTGTA 61 488
9-R CCCTTCGGGAAGAAGCTCTA