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. 2006 Mar 1;7:15. doi: 10.1186/1471-2350-7-15

Table 2.

Primers used to generate the haplotype

Marker Chromosome 17 position Forward Primer Reverse Primer Tm (°C) Other
D17S855 38,458,470 GGATGGCCTTTTAGAAAGTGG ACACAGACTTGTCCTACTGCC 57 5 % DMSO†
D17S1322 38,465,161 CTAGCCTGGGCAACAAACGA GCAGGAAGCAGGAATGGAAC 60 --
D17S1323 38,491,793 TAGGAGATGGATTATTGGTG AAGCAACTTTGCAATGAGTG 60 --
D17S1325 38,891,165 AAAGGTGGCAATTCACAGTTG GTGATAAAACTCAGTGGTACTC 65-55* 1× Q solution

All reactions were amplified for 35 cycles [30s@95°C, 30s@Tm, 30s@72°C] and contained 200 uM dCTP/dGTP/dTTP, 24 uM dATP, 10 uCi α35S-dATP, 1× PCR buffer and 0.5 U of HotStar Taq DNA polymerase (QIAGEN). †Dimethyl Sulfoxide. *Tm starting at 65°C and decreasing by 1°C per cycle for 10 cycles, followed by 25 cycles at 55°C; Q solution from QIAGEN.