Table 1.

Primer pairs and PCR conditions for sequencingWAS cDNA

Primer Set Sequence (5′-3′) Exons CoveredFragment Size (bp*)
W-2  GCTTCGCCAGAGAAGACAAG 1-4  495  
W-496c  TCCACTTTGCCCTCTGATTCC  
W-452 CTCGTGCAGGAGAAGATACA  4-9  475  
W-926c CCTGGTCCTCAATGAAGTCG  
W-906  ACGACTTCATTGAGGACCAG  9-11 497  
W-1402c  CTGCAGCGCTGAGCTCTCTG  
W-1406 CCACCACCTCAGAGCTCAGA  11-12  303  
W-1708c TGAGTGTGAGGACCAGGCAG 
Primer Set Sequence (5′-3′) Exons CoveredFragment Size (bp*)
W-2  GCTTCGCCAGAGAAGACAAG 1-4  495  
W-496c  TCCACTTTGCCCTCTGATTCC  
W-452 CTCGTGCAGGAGAAGATACA  4-9  475  
W-926c CCTGGTCCTCAATGAAGTCG  
W-906  ACGACTTCATTGAGGACCAG  9-11 497  
W-1402c  CTGCAGCGCTGAGCTCTCTG  
W-1406 CCACCACCTCAGAGCTCAGA  11-12  303  
W-1708c TGAGTGTGAGGACCAGGCAG 

For all reactions, the amplification mix contained 1.5 mmol/L MgCl2, and the cycling profile was 30 cycles each of 94°C for 30 sec, 57°C for 1 min, and 72°C for 1 min, with a final extension at 72°C for 5 min.

*

Indicates base pair.

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