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strain atcc 12202  (ATCC)


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    ATCC strain atcc 12202
    Strain Atcc 12202, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 48 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 93 stars, based on 48 article reviews
    strain atcc 12202 - by Bioz Stars, 2026-06
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    Strains and plasmids used in this study

    Journal: Journal of Bacteriology

    Article Title: Conjugative Transfer and cis -Mobilization of a Genomic Island by an Integrative and Conjugative Element of Streptococcus agalactiae

    doi: 10.1128/JB.02199-12

    Figure Lengend Snippet: Strains and plasmids used in this study

    Article Snippet: In addition, they have the same genetic background than the recipient S. pyogenes strain, as shown by pulsed-field gel electrophoresis ( ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window Fig 3 caption a7 Analysis of eight clones of transconjugants obtained after filter-mating experiments between donor strain 515 (carrying ICE_ 515_tRNA Lys ) and recipient strain S. pyogenes ATCC 12202. (A) Amplification of the right junction of the ICEs in these clones as for donor cells, using primers specific of the integrase genes and of the tRNA Lys gene (lane D).

    Techniques: Plasmid Preparation, Mutagenesis

    Analysis of eight clones of transconjugants obtained after filter-mating experiments between donor strain 515 (carrying ICE_515_tRNALys) and recipient strain S. pyogenes ATCC 12202. (A) Amplification of the right junction of the ICEs in these clones as for donor cells, using primers specific of the integrase genes and of the tRNALys gene (lane D). The negative control is S. pyogenes ATCC 12202, used as recipient cells (lane R). Lane M shows DNA molecular weight marker. (B) Analysis of the transconjugants by pulsed-field gel electrophoresis in parallel to the donor strain (lane D) and the recipient strain (lane R).

    Journal: Journal of Bacteriology

    Article Title: Conjugative Transfer and cis -Mobilization of a Genomic Island by an Integrative and Conjugative Element of Streptococcus agalactiae

    doi: 10.1128/JB.02199-12

    Figure Lengend Snippet: Analysis of eight clones of transconjugants obtained after filter-mating experiments between donor strain 515 (carrying ICE_515_tRNALys) and recipient strain S. pyogenes ATCC 12202. (A) Amplification of the right junction of the ICEs in these clones as for donor cells, using primers specific of the integrase genes and of the tRNALys gene (lane D). The negative control is S. pyogenes ATCC 12202, used as recipient cells (lane R). Lane M shows DNA molecular weight marker. (B) Analysis of the transconjugants by pulsed-field gel electrophoresis in parallel to the donor strain (lane D) and the recipient strain (lane R).

    Article Snippet: In addition, they have the same genetic background than the recipient S. pyogenes strain, as shown by pulsed-field gel electrophoresis ( ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window Fig 3 caption a7 Analysis of eight clones of transconjugants obtained after filter-mating experiments between donor strain 515 (carrying ICE_ 515_tRNA Lys ) and recipient strain S. pyogenes ATCC 12202. (A) Amplification of the right junction of the ICEs in these clones as for donor cells, using primers specific of the integrase genes and of the tRNA Lys gene (lane D).

    Techniques: Clone Assay, Amplification, Negative Control, Molecular Weight, Marker, Pulsed-Field Gel, Electrophoresis