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carnobacterium divergens  (ATCC)


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    Structured Review

    ATCC carnobacterium divergens
    STEC, LAB, and spoilage bacteria which selected to perform the biofilm-forming ability test.
    Carnobacterium Divergens, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/carnobacterium divergens/product/ATCC
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    carnobacterium divergens - by Bioz Stars, 2024-12
    93/100 stars

    Images

    1) Product Images from "Formation and Transfer of Multi-Species Biofilms Containing E. coli O103:H2 on Food Contact Surfaces to Beef"

    Article Title: Formation and Transfer of Multi-Species Biofilms Containing E. coli O103:H2 on Food Contact Surfaces to Beef

    Journal: Frontiers in Microbiology

    doi: 10.3389/fmicb.2022.863778

    STEC, LAB, and spoilage bacteria which selected to perform the biofilm-forming ability test.
    Figure Legend Snippet: STEC, LAB, and spoilage bacteria which selected to perform the biofilm-forming ability test.

    Techniques Used:

    Factorial design of strains combination.
    Figure Legend Snippet: Factorial design of strains combination.

    Techniques Used:

    Recovery of STEC O103:H2 after 24 h of enrichment from multispecies dry biofilms stored for 30 days at 10 and 25°C.
    Figure Legend Snippet: Recovery of STEC O103:H2 after 24 h of enrichment from multispecies dry biofilms stored for 30 days at 10 and 25°C.

    Techniques Used:



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    Image Search Results


    STEC, LAB, and spoilage bacteria which selected to perform the biofilm-forming ability test.

    Journal: Frontiers in Microbiology

    Article Title: Formation and Transfer of Multi-Species Biofilms Containing E. coli O103:H2 on Food Contact Surfaces to Beef

    doi: 10.3389/fmicb.2022.863778

    Figure Lengend Snippet: STEC, LAB, and spoilage bacteria which selected to perform the biofilm-forming ability test.

    Article Snippet: Carnobacterium divergens , ATCC 35677 , Vacuum package minced beef , LAB.

    Techniques:

    Factorial design of strains combination.

    Journal: Frontiers in Microbiology

    Article Title: Formation and Transfer of Multi-Species Biofilms Containing E. coli O103:H2 on Food Contact Surfaces to Beef

    doi: 10.3389/fmicb.2022.863778

    Figure Lengend Snippet: Factorial design of strains combination.

    Article Snippet: Carnobacterium divergens , ATCC 35677 , Vacuum package minced beef , LAB.

    Techniques:

    Recovery of STEC O103:H2 after 24 h of enrichment from multispecies dry biofilms stored for 30 days at 10 and 25°C.

    Journal: Frontiers in Microbiology

    Article Title: Formation and Transfer of Multi-Species Biofilms Containing E. coli O103:H2 on Food Contact Surfaces to Beef

    doi: 10.3389/fmicb.2022.863778

    Figure Lengend Snippet: Recovery of STEC O103:H2 after 24 h of enrichment from multispecies dry biofilms stored for 30 days at 10 and 25°C.

    Article Snippet: Carnobacterium divergens , ATCC 35677 , Vacuum package minced beef , LAB.

    Techniques:

    a Schematic illustration of precise control of integrin ligand presentation on nanofilaments via peptide assembly. b TEM images of nanofilaments obtained via molecular self-assembly and co-assembly of FFFIKLLI (100 μM) and FFF at various ratios, and the estimated molecular packing structures. IKLLI motif is presented in blue and FFF motif is presented in pink. The scale bars represent 200 nm. Three independent experiments were performed. c Zoom-in SEM images (false color) of HuH-7 cell edge and apical membrane after 3-day incubations. FFFIKLLI was maintained at a concentration of 100 μM. The cell body is highlighted in pink, while the nanofilaments are highlighted in blue. The scale bars represent 300 nm.

    Journal: Nature Communications

    Article Title: Control cell migration by engineering integrin ligand assembly

    doi: 10.1038/s41467-022-32686-2

    Figure Lengend Snippet: a Schematic illustration of precise control of integrin ligand presentation on nanofilaments via peptide assembly. b TEM images of nanofilaments obtained via molecular self-assembly and co-assembly of FFFIKLLI (100 μM) and FFF at various ratios, and the estimated molecular packing structures. IKLLI motif is presented in blue and FFF motif is presented in pink. The scale bars represent 200 nm. Three independent experiments were performed. c Zoom-in SEM images (false color) of HuH-7 cell edge and apical membrane after 3-day incubations. FFFIKLLI was maintained at a concentration of 100 μM. The cell body is highlighted in pink, while the nanofilaments are highlighted in blue. The scale bars represent 300 nm.

    Article Snippet: Integrin β1 shRNA plasmid (#sc-29375-SH), Integrin α3 shRNA plasmid (#sc-35684-SH), Integrin α6 shRNA plasmid (#sc-43129-SH), and control shRNA plasmid-A (#sc-108060) were purchased from Santa Cruz Biotechnology for knockdown of the target integrins.

    Techniques: Concentration Assay

    a Time-lapse series showing actin cytoskeleton (grey) and paxillin (green) in HuH-7 cells expressing mRuby-Lifeact-7 and mGFP-paxillin upon the treatment of FFFIKLLI (100 μM) for 12 hr. Scale bars represent 2 μm. Three independent experiments were performed. b F-actin phalloidin staining (magenta), integrin β1 (cyan) and paxillin (yellow) immunofluorescence in HuH-7 cell after 12 h treatment of FFFIKLLI (100 μM). Scale bar represents 2 μm. c Fluorescence intensity distribution profile of integrin β1, paxillin, and actin cytoskeleton along the yellow line on merged image of b . d 12 h time course Rac1 activity of HuH-7 cells with or without the treatment of FFFIKLLI (100 μM). Rac1 activity was measured by FRET. n = 6 cells (Ctrl) or 5 cells (FFFIKLLI). Symbols represent the mean FRET/CFP emission ratio ± s.d. e Representative FRET/CFP ratio images of HuH-7 cells expressing RaichuEV-Rac1 with or without the treatment of FFFIKLLI (100 μM) at the indicated time points and coded according to a pseudo-color scale, which ranges from yellow to purple with an increase in Rac1 activity. Scale bars represent 20 μm. Source numerical data are available in source data.

    Journal: Nature Communications

    Article Title: Control cell migration by engineering integrin ligand assembly

    doi: 10.1038/s41467-022-32686-2

    Figure Lengend Snippet: a Time-lapse series showing actin cytoskeleton (grey) and paxillin (green) in HuH-7 cells expressing mRuby-Lifeact-7 and mGFP-paxillin upon the treatment of FFFIKLLI (100 μM) for 12 hr. Scale bars represent 2 μm. Three independent experiments were performed. b F-actin phalloidin staining (magenta), integrin β1 (cyan) and paxillin (yellow) immunofluorescence in HuH-7 cell after 12 h treatment of FFFIKLLI (100 μM). Scale bar represents 2 μm. c Fluorescence intensity distribution profile of integrin β1, paxillin, and actin cytoskeleton along the yellow line on merged image of b . d 12 h time course Rac1 activity of HuH-7 cells with or without the treatment of FFFIKLLI (100 μM). Rac1 activity was measured by FRET. n = 6 cells (Ctrl) or 5 cells (FFFIKLLI). Symbols represent the mean FRET/CFP emission ratio ± s.d. e Representative FRET/CFP ratio images of HuH-7 cells expressing RaichuEV-Rac1 with or without the treatment of FFFIKLLI (100 μM) at the indicated time points and coded according to a pseudo-color scale, which ranges from yellow to purple with an increase in Rac1 activity. Scale bars represent 20 μm. Source numerical data are available in source data.

    Article Snippet: Integrin β1 shRNA plasmid (#sc-29375-SH), Integrin α3 shRNA plasmid (#sc-35684-SH), Integrin α6 shRNA plasmid (#sc-43129-SH), and control shRNA plasmid-A (#sc-108060) were purchased from Santa Cruz Biotechnology for knockdown of the target integrins.

    Techniques: Expressing, Staining, Immunofluorescence, Fluorescence, Activity Assay

    FIC index values of five developed consortia against panel of spoilage and pathogenic strains <xref ref-type= a " width="100%" height="100%">

    Journal: Microbiology Spectrum

    Article Title: Bacteriocin-Based Synergetic Consortia: a Promising Strategy to Enhance Antimicrobial Activity and Broaden the Spectrum of Inhibition

    doi: 10.1128/spectrum.00406-21

    Figure Lengend Snippet: FIC index values of five developed consortia against panel of spoilage and pathogenic strains a

    Article Snippet: Carnobacterium divergence ATCC 35677 , FIC = 0.375 , — , — , — , FIC = 0.625.

    Techniques: