Table 1

Primer sequences and reaction conditions used for amplification of viral and myoglobin sequences (Y = C + T)

Sequence amplified Primer sequence Annealing temp MgCl2(mM) No of cycles Amplicon (bp)
Enterovirus 5′ UTR First round PCR 50°C2.030228
Nucleotide positions 417–645
5′-GGTGYGAAGAGYCTAYTGAG
5′-CACYGGATGGCYATTCCA
Nested reaction 52°C1.825146
Nucleotide positions 456–602
5′-CCCCTGAATGCGGCTAAT
5′-ATTGTCACCATAAGCAGCCA
HCMV UL83 region First round PCR 57°C1.540449
Nucleotide positions 120032–120489
5′-TCTCGCGTATGGCTTG
5′-GTCAGCGTTCGTGTTTCC
Nested reaction 55°C1.530233
Nucleotide positions 120144–120377
5′-TGAGGTAAAAGCCACATCCAG
5′-GACCAGTACGTCAAGGTGTAC
Adenovirus hexon region First round PCR 60°C2.040300
Nucleotide positions 18858–19158
5′-GCCGCAGTGGTCTTACATGCACATC
5′-CAGCACGCCGCGGATGTCAAAGT
Nested reaction 60°C2.030142
Nucleotide positions 18937–19079
5′-GCCACCGAGACGTACTTCAGCCTG
5′-TTGTACGAGTACGCGGTATCCTCGCGGTC
Myoglobin exons 1 and 3 Amplification from DNA 55°C1.535439
5′-AACATGACAGGTCCTCTTGG
5′-CATGGCGCAGTCTGAA
Amplification from cDNA 55°C1.540299
5′TTGGCAGGAAGTCCTCATCA
5′-AGCTCCAGGGCCTTGTTCAT
  • bp, base pair; HCMV UL83, human cytomegalovirus unique long; PCR, polymerase chain reaction.