SEARCH

SEARCH BY CITATION

Appendix S1. Materials and methods.

Fig. S1. DGGE analysis of pure culture isolates, lanes 1–13.

Fig. S2. DGGE analysis of pure culture isolates, lanes 14–25.

Fig. S3. DGGE analysis of pure culture isolates, lanes 26 and 27.

Fig. S4. PCR products of the new rpoB-DGGE primers amplified and run on a 1.2% agarose gel with 1X TAE buffer.

Fig. S5. PCR products of the large amplifying new rpoB primers amplified and run on a 1.2% agarose gel with 1X TAE buffer.

Table S1. Bacterial pure cultures used in this study to test newly developed rpoB primers.

Table S2. Reference bacterial strains used for the development of rpoB primers in this study.

Table S3. 16S rRNA gene-V3 (Bovine).

Table S4. 16S rRNA gene-V3 (Ovine).

Table S5.rpoB-Dahllöf (Bovine).

Table S6.rpoB-Dahllöf (Ovine).

Table S7.rpoB – this study (Bovine).

Table S8.rpoB – this study (Ovine).

Please note: Wiley-Blackwell is not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article.

FilenameFormatSizeDescription
FEM_1042_sm_supplemental-material.doc786KSupporting info item

Please note: Wiley Blackwell is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.