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. 2008 Dec 10;4(3):216–220. doi: 10.1007/s11671-008-9228-z

Table 1.

Target oligonucleotide sequences

ssDNA No. Sequence (5′-3′)
175wd
 
GGCACCCGCGTCCGCGCCATGGCCATCTAC
175G–A
1
GGCACCCGCGTCCCGCCATGGCCATCTAC
245wd
 
TGCATGGGCGGCATGAACCGGAGGCCCATC
245G–T
2
TGCATGGGCGCATGAACCGGAGGCCCATC
245G–A
3
TGCATGGGCGCATGAACCGGAGGCCCATC
248wd
 
GCATGAACCGGAGGCCCATCCTCACCATCA
248G–A
4
GCATGAACCGAGGCCCATCCTCACCATCA
248G–T
5
GCATGAACCGAGGCCCATCCTCACCATCA
248C–T
6
GCATGAACGGAGGCCCATCCTCACCATCA
249wd
 
GCATGAACCGGAGGCCCATCCTCACCATCA
249G1–T
7
GCATGAACCGGAGCCCATCCTCACCATCA
249G2–T
8
GCATGAACCGGAGCCCATCCTCACCATCA
249G-C
9
GCATGAACCGGAGCCCATCCTCACCATCA
273wd
 
GAACAGCTTTGAGGTGCGTGTTTGTGCCTG
273G–T
10
GAACAGCTTTGAGGTGCTGTTTGTGCCTG
273G–A
11
GAACAGCTTTGAGGTGCTGTTTGTGCCTG
282wd
 
TCCTGGGAGAGACCGGCGCACAGAGGAAGA
282C–T 12 TCCTGGGAGAGACGGCGCACAGAGGAAGA

The underline corresponds to the single base mismatch comparing with the wildtype (wd). 12 of the most frequent point mutations in exon 5, 7, and 8 of human p53 gene are included. 248wd and 249wd are the same sequences. The mutant sequences are numbered from 1 to 12