Skip to main content
. 2007 Jan 17;45(3):1042–1044. doi: 10.1128/JCM.01109-06

TABLE 1.

Primers, probes, and PCR specifications used for amplification of various parts of the MIE genea

Primer/probe designation Sequence, 5′→3′ Genomic coordinateb Cycling conditions
RQ1 GACTAGTGTGATGCTGGCCAAG 2719 95°C/10 min → 50 times (95°C/15 s → 60°C/1 min)
RQ2 GCTACAATAGCCTCTTCCTCATCTG 2919
RQ probe AGCCTGAGGTTATCAGTGTAATGAAGCGCC 2758
CMV 2-4F GACCCTGATAATCCTGACGA 1506 95°C/10 min → 35 times (95°C/30 s → 53°C/30 s →
CMV 2-4R ATGTGCTCCTTGATTCTATG 2073     72°C/30 s) → 72°C/7 min
exon4celyF GAAATTCACTGGCGCCTTTA 2101 95°C/3 min → 35 times (95°C/1 min → 53°C/1 min →
exon4celyR AGCACCATCCTCCTCTTCCT 3169     72°C/2 min) → 72°C/7 min
CMV4F AGTGAGTTCTGTCGGGTGCT 2678 95°C/3 min → 25 times (95°C/30 s → 53°C/30 s →
CMV4R CCCTCCTCCTCTTCCTCATC 3075     72°C/1 min) → 72°C/7 min
a

RQ1, RQ2, and RQ probe, primers and probe for Q-PCR; CMV 2-4F and CMV 2-4R, primers for qualitative PCR; exon4celyF, exon4celyR, CMV4F, and CMV4R, primers for nested PCR and consecutive sequencing.

b

MIE gene sequence (GenBank accession no. M21295).