Table 1

Primer sequences, PCR conditions, temperatures, and temperature gradients used for DHPLC mutation screening of genes K8 and K18

ExonSequenceMgCl2Anealing tempProduct sizeTemp gradient
Temp, temperature.
K8 Ex1 5′5′-AGAAGCAGCTTCTCCGCTC-3′
K8 Ex1 3′5′-GGACTACCAGGAGAAAGGGG-3′2.0 mM64.1°C45262.5–65.5°C
K8 Ex2 5′5′- AAAAGACTGCTTGCTTTCCTC -3′
K8 Ex2 3′5′- AGGTGACTTCAGTTGGGTGG -3′1.5 mM64.1°C32260.0–62.0°C
K8 Ex3 5′5′- AGGGCAACCTCCCTTTTG -3′
K8 Ex3 3′5′- CAGTGTCCAGATAGGAGAAGGG -3′2.0 mM64.1°C14859.5+60.5°C
K8 Ex4 5′5′- GGCTCCCCTCTCCTCATC -3′
K8 Ex4 3′5′- TCTCCTGCGACCAGGAAC -3′2.0 mM62.7°C14260.0+61.0°C
K8 Ex5 5′5′- ACCACTTGCCCTCTTCCC -3′
K8 Ex5 3′5′- AGCTGAACTGTGGCTGCC -3′1.5 mM65.6°C45860.0–62.0°C
K8 Ex6 5′5′- GAAGAGAAGGCATACCCAACC -3′
K8 Ex6 3′5′- ACAGGACCCCAAGTCCAAG -3′1.5 mM65.6°C37363.5–65.5°C
K8 Ex7 5′5′- GAAGGGCTAGGAGTTGGTCC -3′
K8 Ex7 3′5′- TGAGCGACTGAGCACAGC -3′1.5 mM65.6°C18861.0–66.0°C
K8 Ex8 5′5′- TGTGGCTACCTCTGTCCCTC -3′
K8 Ex8 3′5′- GAGGGGTAGGCTGGGAGG -3′1.5 mM62.7°C24664.0–66.0°C
K18 Ex1 5′5′- CCTGTCCTTTCTCTCTCCCC -3′
K18 Ex1 3′5′- TCCCTCCTACCCCTTACCTG -3′1.5 mM61.3°C46162.0–67.0°C
K18 Ex2 5′5′- TGGGACCAGGAAGTTTTCAC -3′
K18 Ex2 3′5′- GTCCTTCTTAGCTCCACCCC -3′1.5 mM62.7°C24160.0+61.0°C
K18 Ex3 5′5′- TGGATCAGAGATAGGGGCC -3′
K18 Ex3 3′5′- TTCTCTTGGCCCCTCAATC -3′1.5 mM62.7°C24862.0+63.0°C
K18 Ex4 5′5′- AGAGGCAATCACAGAAGAAAGG -3′
K18 Ex4 3′5′- CACACCTTGGCAGCCATC -3′1.5 mM62.7°C27660.5–63.5°C
K18 Ex5 5′5′- TCTCAGCAGGTGCGTGAG -3′
K18 Ex5 3′5′- GGGCAGGTGATGTGAAGG -3′1.5 mM62.7°C24561.5–63.5°C
K18 Ex6 5′5′- GATGAGCAGTCCTGGGACTC -3′
K18 Ex6 3′5′- CAGTGAACAGACACATGGGG -3′1.5 mM62.7°C37762.0–64.0°C
K18 Ex7 5′5′- GCTGTTTATAACTTGGGCTTGG -3′
K18 Ex7 3′5′- TCCTGCTCCCAAAGGGTAC -3′1.5 mM62.7°C19061.0+62.0°C