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. Author manuscript; available in PMC: 2008 Aug 8.
Published in final edited form as: Anal Chem. 2006 May 1;78(9):3158–3164. doi: 10.1021/ac0600151

Table 1.

Summary of all DNA sequences used for the ligation reaction, nanoparticle-enhanced SPRI detection and PCR amplification

Array probes (Immobilized on the DNA microarray):
PG = 5′-S-S-(CH2)6-(T)20 GTG CTT TGT TCT GGA TTT CG -3′
PC = 5′-S-S-(CH2)6-(T)20 GTG CTT TGT TCT GGA TTT CC -3′
PA = 5′-S-S-(CH2)6-(T)20 GTG CTT TGT TCT GGA TTT CA -3′
PN = 5′-S-S-(CH2)6-(T)40 -3′
Oligonucleotide Target (Location of the targeted single base pair is underlined):
T = 5′-TGC CCT TGA GGA CCT GCG AAA TCC AGA ACA AAG CAC -3′
Ligation Probe:
L = 5′-PO4 CAG GTC CTC AAG GGC A -3′
Ligation Probe Complement (Attached to gold nanoparticles):
LC = 5′-S-S-(CH2)6-(T)20 TGC CCT TGA GGA CCT G -3′
PCR primers for exon 13 of BRCA1 gene:
Forward: 5′-AAT GGA AAG CTT CTC AAA GTA -3′
Reverse: 5′-ATG TTG GAG CTA GGT CCT TAC -3′