Skip to main content
. 2001 Nov;67(11):4984–4991. doi: 10.1128/AEM.67.11.4984-4991.2001

FIG. 2.

FIG. 2

Specificity of detection of selected Salmonella serovar Enteritidis phage type reference strains determined using the Sdf I primer pair in PCRs. The strains used are from the NVSL unless indicated by a specific designation. (A) Detection of Sdf I in phage type reference strains. Lane M, size markers; lane 1, CAHFS-546 (positive control); lane 2, no template; lane 3, phage type 2; lane 4, phage type 3; lane 5, phage type 4; lane 6, phage type 6; lane 7, phage type 6A; lane 8, phage type 8; lane 9, phage type 9; lane 10, phage type 9A; lane 11, phage type 13A; lane 12, 95-13141 (phage type 14B); lane 13, phage type 24; lane 14, phage type 34. (B) Detection of Sdf I in phage type reference strains and clinical strains of phage types 6A, 6B, and 9A. Lane M, size markers; lane 1, CAHFS-546 (positive control); lane 2, no template; lane 3, NVSL 9 (phage type 6A); lane 4, CAHFS-435 (phage type 6A); lane 5, CAHFS-436 (phage type 6A); lane 6, CAHFS-739 (phage type 6B); lane 7, NVSL 13 (phage type 9A); lane 8, D0144-CDC (phage type 9A); lane 9, D01760-CDC (phage type 9A). Amplicons produced by the Sdf I primers (293 bp) and rplI primers (343 bp) are indicated.