Skip to main content
. 2013 Jan;79(1):322–327. doi: 10.1128/AEM.02632-12

Table 2.

Primers and probe used in this study

Gene Forward sequence (5′→3′) Reverse sequence (5′-→3′) Probe sequence (5′→3′)d Amplicon size (bp) Reference
gltA GGGGACCAGCTCATGGTGG AATGCAAAAAGAACAGTAAACA NA ∼350 22
gltAa GGGGACCAGCTCATGGTGG CGTGGATCATAATTTTTATA CCAAAACCCATAAGGCGGAAAGGATCATTT ∼143 19
gltAb GTTATCCTATTGACCAA CCAAAACCCATAAGGCG NA ∼685 20
AACTCTTGCCGCTATGG TATTCTTCACAAGGAAC ∼401/387c
rpoB GCACGATTYGCATCATCTTTTCC CGCATTATGGTCGTATTTGTCC NA ∼333 21
groEL ATGGACAAAGTTGGCAATGAA TTCCACCACCAGCAACAATA NA ∼720 This study
ribC TAACCGATATTGGTTGTGTTGAAG TAAAGCTAGAAAGTCTGGCAACATAACG NA ∼588 This study
ftsZ CATATGGTTTTCATTACTGCYGGTATGG TTCTTCGCGAATACGATTAGCAGCTTC NA ∼515 21
a

qPCR.

b

Seminested PCR.

c

Seminested PCR product.

d

Dually labeled oligonucleotide probe with 5′-6-carboxyfluorescein and 3′-black hole quencher 1. NA, not applicable.