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. 2016 Aug 5;6(3):197–205. doi: 10.1556/1886.2016.00004

Table 2.

ipaH and lacY primers and probes used in the present study

Gene Primer or probe* Sequence (5′–3′) Melting point (°C) PCR product (bp) Fluorochrome (5′ end) Reference
lacY lacY-F ACCAGACCCAGCACCAGATAAG 59 104 [19]
lacY-R TTCTGCTTCTTTAAGCAACTGGC 58.9 Modified from [19]
lacY-MGB-p1 CATACATATTGCCCGCCAGTA 70 FAM Modified from [19]
lacY-MGB-p2 CATACATATGCCCGCCAGA 70 FAM Modified from [19]
ipaH ipaH-F GACGGACAACAGAATACACTCCATC 59.8 108 Modified from [22]
ipaH-R ATGTTCAAAAGCATGCCATATCTGT 59.8 [22]
ipaH-MGB-p CGGAAAACAAACAATCTGATGT 69 VIC Modified from [22]

*All probes were conjugated with minor groove binder (MGB) and had a “Black Hole Quencher” at the 3′ end

Due to sequence variation in the lacY gene of certain EIEC strains, two different lacY probes were used to detect all EIEC strains [19]