shigellaflexner  (ATCC)


Bioz Verified Symbol ATCC is a verified supplier
Bioz Manufacturer Symbol ATCC manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94

    Structured Review

    ATCC shigellaflexner
    Shigellaflexner, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/shigellaflexner/product/ATCC
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    shigellaflexner - by Bioz Stars, 2022-09
    94/100 stars

    Images

    Similar Products

  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 94
    ATCC shigella flexneri
    Scanning electron microscope image of the synthesized vancomycin-coated iron oxide magnetic nanoparticles ( upper left panel). Schematic illustration of the MNP@antibiotic agglutination test ( upper right panel). Evaluation of the interaction between two antibiotics, penicillin and vancomycin, stabilized magnetic beads with the two bacterial strains, B. cereus and S. <t>flexneri</t> , using the MNP@antibiotic agglutination test ( lower panel).
    Shigella Flexneri, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/shigella flexneri/product/ATCC
    Average 94 stars, based on 3 article reviews
    Price from $9.99 to $1999.99
    shigella flexneri - by Bioz Stars, 2022-09
    94/100 stars
      Buy from Supplier

    Image Search Results


    Scanning electron microscope image of the synthesized vancomycin-coated iron oxide magnetic nanoparticles ( upper left panel). Schematic illustration of the MNP@antibiotic agglutination test ( upper right panel). Evaluation of the interaction between two antibiotics, penicillin and vancomycin, stabilized magnetic beads with the two bacterial strains, B. cereus and S. flexneri , using the MNP@antibiotic agglutination test ( lower panel).

    Journal: Biosensors

    Article Title: Magnetic Separation and Centri-Chronoamperometric Detection of Foodborne Bacteria Using Antibiotic-Coated Metallic Nanoparticles

    doi: 10.3390/bios11070205

    Figure Lengend Snippet: Scanning electron microscope image of the synthesized vancomycin-coated iron oxide magnetic nanoparticles ( upper left panel). Schematic illustration of the MNP@antibiotic agglutination test ( upper right panel). Evaluation of the interaction between two antibiotics, penicillin and vancomycin, stabilized magnetic beads with the two bacterial strains, B. cereus and S. flexneri , using the MNP@antibiotic agglutination test ( lower panel).

    Article Snippet: LB agar growth medium was obtained from Merck, France, and was used to replicate S. flexneri (ATCC 29903 ) and B. cereus (ATCC 11768 ) , available as reference strains from the Laboratory of Epidemiology and Veterinary Microbiology at Pasteur Institute of Tunis.

    Techniques: Microscopy, Synthesized, Agglutination, Magnetic Beads

    Chronoamperometric curves correspond to the response of the centri-chronoamperometric assay without bacteria (noninoculated LB media) and with various S. flexneri concentrations: 1.44, 2.88, 5.75, 11.5, and 23 cells/mL ( A ). Biosensor response to various concentration of S. flexneri . The curve indicates the fitting of the experimental data with a logarithmic regression (current density) = 0.1526 × ln ( S. flexneri concentration) + 0.7168 (R2 = 0.9486) ( B ).

    Journal: Biosensors

    Article Title: Magnetic Separation and Centri-Chronoamperometric Detection of Foodborne Bacteria Using Antibiotic-Coated Metallic Nanoparticles

    doi: 10.3390/bios11070205

    Figure Lengend Snippet: Chronoamperometric curves correspond to the response of the centri-chronoamperometric assay without bacteria (noninoculated LB media) and with various S. flexneri concentrations: 1.44, 2.88, 5.75, 11.5, and 23 cells/mL ( A ). Biosensor response to various concentration of S. flexneri . The curve indicates the fitting of the experimental data with a logarithmic regression (current density) = 0.1526 × ln ( S. flexneri concentration) + 0.7168 (R2 = 0.9486) ( B ).

    Article Snippet: LB agar growth medium was obtained from Merck, France, and was used to replicate S. flexneri (ATCC 29903 ) and B. cereus (ATCC 11768 ) , available as reference strains from the Laboratory of Epidemiology and Veterinary Microbiology at Pasteur Institute of Tunis.

    Techniques: Concentration Assay

    Phage plaques formed in double-layer agar plates and electron micrograph of negatively stained phage pSs-1. ( A ) phage plaques formed in agar plates with S. sonnei ATCC ® 25931, ( B ) phage plaques formed in agar plates with S. flexneri ATCC ® 29903, and ( C ) electron micrograph of pSs-1. The bar corresponds to 50 nm.

    Journal: Scientific Reports

    Article Title: Bacteriophage application to control the contaminated water with Shigella

    doi: 10.1038/srep22636

    Figure Lengend Snippet: Phage plaques formed in double-layer agar plates and electron micrograph of negatively stained phage pSs-1. ( A ) phage plaques formed in agar plates with S. sonnei ATCC ® 25931, ( B ) phage plaques formed in agar plates with S. flexneri ATCC ® 29903, and ( C ) electron micrograph of pSs-1. The bar corresponds to 50 nm.

    Article Snippet: To evaluate the bacteriolytic activity of pSs-1 against S. sonnei ATCC® 25931 and S. flexneri ATCC® 29903, the absorbance (OD600 nm ) was examined in order to determine the change of viable bacteria.

    Techniques: Staining

    Time course of host cell lysis effect of pSs-1 against S. sonnei ATCC ® 25931 ( A ) and S. flexneri ATCC ® 29903 ( B ). Early exponential phase cultures of S. sonnei ATCC ® 25931 and S. flexneri ATCC ® 29903 were co-cultured with pSs-1 at MOIs of 0, 0.1, 1, and 10. The results are shown as mean + standard deviations from triplicate experiments.

    Journal: Scientific Reports

    Article Title: Bacteriophage application to control the contaminated water with Shigella

    doi: 10.1038/srep22636

    Figure Lengend Snippet: Time course of host cell lysis effect of pSs-1 against S. sonnei ATCC ® 25931 ( A ) and S. flexneri ATCC ® 29903 ( B ). Early exponential phase cultures of S. sonnei ATCC ® 25931 and S. flexneri ATCC ® 29903 were co-cultured with pSs-1 at MOIs of 0, 0.1, 1, and 10. The results are shown as mean + standard deviations from triplicate experiments.

    Article Snippet: To evaluate the bacteriolytic activity of pSs-1 against S. sonnei ATCC® 25931 and S. flexneri ATCC® 29903, the absorbance (OD600 nm ) was examined in order to determine the change of viable bacteria.

    Techniques: Lysis, Cell Culture

    ( A ) MDR Staphylococcal strains discriminated by universally conserved thermonuclease ( nuc ) gene. Isolated 160 Staphylococcal spp., were screened to identify at species level by PCR using universally conserved thermonuclease ( nuc ) gene. PCR confirmed as 151 methicillin resistant S . aureus (Lane 1–4, 359 bp), 6 as S . epidermidis (Lane 5–8, 251 bp) and 2 as S . haemolyticus (Lane 9 and 10, 434 bp) used along with E . coli (Lane 11), S . typhimurium (Lane 12), S . flexneri (Lane 13), V . cholera (Lane 14), and V . parahaemolyticus (Lane 15) were compared with 100 bp ladder (M) and water as negative control (C-). ( B) Illustration of PCR amplicons expected when using the updated Staphylococcal spp. multiplex PCR. Lane M, 100 bp ladder; Lane 1, negative control (C-); Lane 2, mixture of multiplex PCR products obtained for all the templates of MDR-MRSA, MRSE, MRSH and S . typhimurium; Lane 3, MRSA; Lane 4, MRSE ; Lane 5, MRSH and Lane 6, S . typhimurium comparable to the amplified product of mPCR in lane 2.

    Journal: Scientific Reports

    Article Title: MALDI-TOF-MS based identification and molecular characterization of food associated methicillin-resistant Staphylococcus aureus

    doi: 10.1038/s41598-017-11597-z

    Figure Lengend Snippet: ( A ) MDR Staphylococcal strains discriminated by universally conserved thermonuclease ( nuc ) gene. Isolated 160 Staphylococcal spp., were screened to identify at species level by PCR using universally conserved thermonuclease ( nuc ) gene. PCR confirmed as 151 methicillin resistant S . aureus (Lane 1–4, 359 bp), 6 as S . epidermidis (Lane 5–8, 251 bp) and 2 as S . haemolyticus (Lane 9 and 10, 434 bp) used along with E . coli (Lane 11), S . typhimurium (Lane 12), S . flexneri (Lane 13), V . cholera (Lane 14), and V . parahaemolyticus (Lane 15) were compared with 100 bp ladder (M) and water as negative control (C-). ( B) Illustration of PCR amplicons expected when using the updated Staphylococcal spp. multiplex PCR. Lane M, 100 bp ladder; Lane 1, negative control (C-); Lane 2, mixture of multiplex PCR products obtained for all the templates of MDR-MRSA, MRSE, MRSH and S . typhimurium; Lane 3, MRSA; Lane 4, MRSE ; Lane 5, MRSH and Lane 6, S . typhimurium comparable to the amplified product of mPCR in lane 2.

    Article Snippet: Salmonella typhimurium (98), Escherichia coli (1610), Staphylococcus aureus (96), Bacillus cereus (430), Shigella flexneri (1457), Vibrio cholera (3904), Vibrio paraheamolyticus (451), Pseudomonas aeruginosa (1688) and Enterobacter aerogenes (13048) strains were cultured as per the protocol prescribed by MTCC and ATCC.

    Techniques: Isolation, Polymerase Chain Reaction, Negative Control, Multiplex Assay, Amplification