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. 2005 Aug 21;11(31):4891–4894. doi: 10.3748/wjg.v11.i31.4891

Table 1.

Primer sequences and restriction enzymes of mutation in Se and Le genes

Mutation Primer sequence Enzyme
Se gene
A385T UP1: GATGGAGGAGGAATACCGCCTC Ear I
DP2: GATCTCCTGGCGGAGGTGGTGGTAGAAGATC
G428A Identical to A358T primer pairs Bgl II
C571T UP: AGGAGATCCTCCAGGAGTTCA Dde I
DP: AGAAGGAGAAAAGGTCTCAAAGG
G849A Identical to C571T primer pairs Dde I
C628T UP: AGTGTGGAAGGGGGTGGTGCCC Bgl I
DP: CCACTCTGGCAGGAAGGC
Fusion gene UP: CTGCCTCCTGACCATGTCC Pst I
DP: identical to reverse primer of C628T
Le genes
T202C and C314T UP: CCACCCTCCTGATCCTGCTC Msp I (T202C)
DP: GATATCCCAGTGGTGCACGATGATGATC Bcl I (C314T)
C445A UP: identical to UP of T202 C and C314 T BstN I
DP: GAGATTGAAGTATCTGTCCAAGGC
G508A UP: TCAACTTGGAGCCACACCCT Alu I
DP: AGTTGGACACCGCCCAGGCCACCAG
A1007C UP: GCTCCTTCCGCTGGGCACTAG Alu I
DP: TGGCCACAAAGGACTCCAGC
T1067A UP: GTACCAGACGGTGCGATGCA Nsi I
DP: identical to DP of A1007 C

1UP: upstream primer; 2DP: downstream primer; The mutated base is underlined.