Skip to main content
. 2000 Dec;38(12):4351–4355. doi: 10.1128/jcm.38.12.4351-4355.2000

FIG. 1.

FIG. 1

Agarose gel electrophoresis of the 933-bp PCR amplification products from chromosomal DNA from staphylococcal species reference strains using primers GF-1 and GR-2 (A), from other genera used as negative control (B), and fragments produced by AluI endonuclease digestion of PCR amplification products (C). Lanes: 1, S. aureus CECT 86; 2, S. epidermidis CECT 232; 3, S. capitis CECT 233; 4, S. hominis CECT 234; 5, S. saprophyticus CECT 235; 6, S. warneri CECT 236; 7, S. xylosus CECT 237; 8, S. auricularis CECT 4052; 9, S. carnosus CECT 4491; 10, S. simulans CECT 4538; 11, S. intermedius ATCC 49052; 12, S. haemolyticus human isolate; 13, Streptococcus sp. mastitis isolate; 14, S. agalactiae CECT 183; 15, S. dysagalactiae CECT 758; 16, S. suis CECT 958; 17, B. cereus CECT 193; 18, E. faecalis CECT 795; 19, M. luteus CECT 241; 20, A. hydrophila CECT 839; 21, E. coli CECT 434; 22, S. cholerasuis CECT 556; 23, Y. ruckeri CECT 4319; 24, reaction mixture with no DNA. Lanes M, standard DNA size markers (φX174 digested with HaeIII), (A and B, from top to bottom: 1,353, 1,078, 872, and 603 bp) and 50-bp ladder (C); bottom band, 50 bp.