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phage particles  (Hitachi Ltd)


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    Hitachi Ltd phage particles
    Phage Particles, supplied by Hitachi Ltd, used in various techniques. Bioz Stars score: 99/100, based on 45777 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phage particles/product/Hitachi Ltd
    Average 99 stars, based on 45777 article reviews
    phage particles - by Bioz Stars, 2026-06
    99/100 stars

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    Image Search Results


    Bacteriophage morphology and phenotypic characteristics of FNU2: Capsid length 89.9 ± 0.76 nm, Tail length 325.07 ± 2.33 nm, Tail width 13.55 ± 0.35 nm (A); FNU3: Capsid length 99.36 ± 0.85 nm, Tail length 323.56 ± 2.57 nm, Tail width 14.53 ± 0.25 nm (B); FNU4: Capsid length 56.98 ± 0.2.3 nm, Tail length 156.32 ± 7.5 nm, Tail width 11.44 ± 1.6 nm (C); Genomic alignment of bacteriophage FNU2, FNU3 and FNU4. Homology to FNU4 by FNU2 and FNU3 highlighted by grey connecting lines to the tail region (green) and in genes for DNA, RNA and nucleotide metabolism (yellow) (D).

    Journal: Journal of Oral Microbiology

    Article Title: Characterisation of novel Fusobacterium nucleatum bacteriophages and their efficacy in disrupting pathogenic dual-species biofilms

    doi: 10.1080/20002297.2025.2584952

    Figure Lengend Snippet: Bacteriophage morphology and phenotypic characteristics of FNU2: Capsid length 89.9 ± 0.76 nm, Tail length 325.07 ± 2.33 nm, Tail width 13.55 ± 0.35 nm (A); FNU3: Capsid length 99.36 ± 0.85 nm, Tail length 323.56 ± 2.57 nm, Tail width 14.53 ± 0.25 nm (B); FNU4: Capsid length 56.98 ± 0.2.3 nm, Tail length 156.32 ± 7.5 nm, Tail width 11.44 ± 1.6 nm (C); Genomic alignment of bacteriophage FNU2, FNU3 and FNU4. Homology to FNU4 by FNU2 and FNU3 highlighted by grey connecting lines to the tail region (green) and in genes for DNA, RNA and nucleotide metabolism (yellow) (D).

    Article Snippet: The purified bacteriophage particles were visualised using a JEOL JEM−2100 transmission electron microscope (TEM) with 400-mesh carbon-coated copper grids (ProSciTech, Australia).

    Techniques:

    Proteomic phylogeny of the F. nucleatum bacteriophages. The monophyletic cluster of the Latrobeviruses is highlighted in the dotted green rectangle while the FNU4 bacteriophage is shown in the dotted purple rectangle.

    Journal: Journal of Oral Microbiology

    Article Title: Characterisation of novel Fusobacterium nucleatum bacteriophages and their efficacy in disrupting pathogenic dual-species biofilms

    doi: 10.1080/20002297.2025.2584952

    Figure Lengend Snippet: Proteomic phylogeny of the F. nucleatum bacteriophages. The monophyletic cluster of the Latrobeviruses is highlighted in the dotted green rectangle while the FNU4 bacteriophage is shown in the dotted purple rectangle.

    Article Snippet: The purified bacteriophage particles were visualised using a JEOL JEM−2100 transmission electron microscope (TEM) with 400-mesh carbon-coated copper grids (ProSciTech, Australia).

    Techniques:

    Bacteriophage FNU4 alignment with the contig of the host subspecies unclassified F. nucleatum strain 2256 draft genome.

    Journal: Journal of Oral Microbiology

    Article Title: Characterisation of novel Fusobacterium nucleatum bacteriophages and their efficacy in disrupting pathogenic dual-species biofilms

    doi: 10.1080/20002297.2025.2584952

    Figure Lengend Snippet: Bacteriophage FNU4 alignment with the contig of the host subspecies unclassified F. nucleatum strain 2256 draft genome.

    Article Snippet: The purified bacteriophage particles were visualised using a JEOL JEM−2100 transmission electron microscope (TEM) with 400-mesh carbon-coated copper grids (ProSciTech, Australia).

    Techniques:

    Location of protospacers targeted by F. nucleatum strain 2256 CRISPR system, that are found in the bacteriophage FNU4. The putative genes are represented by packaging (black), hypothetical (grey), head and capsid (green), lysis (red), tail (blue), transport and metabolism (yellow), and DNA manipulation (pink) (A). Genome maps of draft genomes of two of the F. nucleatum hosts for bacteriophages. In both F. nucleatum strain 2256 (B) and Fnp ATCC 10953 (C), the genome maps consist of tracks that are labeled from outside to center as track 1: prophage in dark green; tracks 2 & 3 mobile genetic elements including sites for replication (red), integration or excision (light green), defence-related genes (purple) and other transfer genes (olive green). Track 4 indicates the GC content graph, while the size of the genome is indicated by the labels on the innermost track. The bacteriophage FNU4 has homology to the region from 0.4 Mbp to 0.8 Mbp in the F. nucleatum strain 2256 map. Kernel density estimation (KDE) plots showing the uneven clustering of defence system loci across the genomes of F. nucleatum strains 2256 (D) and Fnp ATCC 10953 (E).

    Journal: Journal of Oral Microbiology

    Article Title: Characterisation of novel Fusobacterium nucleatum bacteriophages and their efficacy in disrupting pathogenic dual-species biofilms

    doi: 10.1080/20002297.2025.2584952

    Figure Lengend Snippet: Location of protospacers targeted by F. nucleatum strain 2256 CRISPR system, that are found in the bacteriophage FNU4. The putative genes are represented by packaging (black), hypothetical (grey), head and capsid (green), lysis (red), tail (blue), transport and metabolism (yellow), and DNA manipulation (pink) (A). Genome maps of draft genomes of two of the F. nucleatum hosts for bacteriophages. In both F. nucleatum strain 2256 (B) and Fnp ATCC 10953 (C), the genome maps consist of tracks that are labeled from outside to center as track 1: prophage in dark green; tracks 2 & 3 mobile genetic elements including sites for replication (red), integration or excision (light green), defence-related genes (purple) and other transfer genes (olive green). Track 4 indicates the GC content graph, while the size of the genome is indicated by the labels on the innermost track. The bacteriophage FNU4 has homology to the region from 0.4 Mbp to 0.8 Mbp in the F. nucleatum strain 2256 map. Kernel density estimation (KDE) plots showing the uneven clustering of defence system loci across the genomes of F. nucleatum strains 2256 (D) and Fnp ATCC 10953 (E).

    Article Snippet: The purified bacteriophage particles were visualised using a JEOL JEM−2100 transmission electron microscope (TEM) with 400-mesh carbon-coated copper grids (ProSciTech, Australia).

    Techniques: CRISPR, Lysis, Labeling

    Mono- and dual-species biofilms imaged via confocal microscopy. F. nucleatum ( Fnp) (green) and P. gingivalis ATCC 33277 ( Pg ) (red) prestained and imaged before biofilm formation (top panel); following biofilm formation (middle panel); biofilms treated with Fnp -specific bacteriophage FNU2 (bottom panel). The biofilms were cultured for up to 48 h (A). 3-D confocal image stack showing (i) attachment of Fnp (green) to cover the slip side and Pg (red) overlaying the Fnp to form a dual-species biofilm. Treatment with (ii) the lytic FNU2 bacteriophage and (iii) the lytic FNU3 bacteriophage disrupted approximately 75% of the biofilm mass. The biofilms were cultured for up to 4 days (B). Quantification of the biofilm-forming capacity of Fnp and P. gingivalis , and their disruption by the Fnp bacteriophages FNU2 and FNU3. The three panels represent Fnp ATCC 10953 mono-species biofilms (C), dual-species biofilms of Fnp ATCC 10953 and P . gingivalis ATCC 33277 (D) and P. gingivalis ATCC 33277 mono-species biofilm (E). Heat-killed F. nucleatum was boiled at 100 ° C for 1 h before being added to P . gingivalis ATCC 33277 biofilm.

    Journal: Journal of Oral Microbiology

    Article Title: Characterisation of novel Fusobacterium nucleatum bacteriophages and their efficacy in disrupting pathogenic dual-species biofilms

    doi: 10.1080/20002297.2025.2584952

    Figure Lengend Snippet: Mono- and dual-species biofilms imaged via confocal microscopy. F. nucleatum ( Fnp) (green) and P. gingivalis ATCC 33277 ( Pg ) (red) prestained and imaged before biofilm formation (top panel); following biofilm formation (middle panel); biofilms treated with Fnp -specific bacteriophage FNU2 (bottom panel). The biofilms were cultured for up to 48 h (A). 3-D confocal image stack showing (i) attachment of Fnp (green) to cover the slip side and Pg (red) overlaying the Fnp to form a dual-species biofilm. Treatment with (ii) the lytic FNU2 bacteriophage and (iii) the lytic FNU3 bacteriophage disrupted approximately 75% of the biofilm mass. The biofilms were cultured for up to 4 days (B). Quantification of the biofilm-forming capacity of Fnp and P. gingivalis , and their disruption by the Fnp bacteriophages FNU2 and FNU3. The three panels represent Fnp ATCC 10953 mono-species biofilms (C), dual-species biofilms of Fnp ATCC 10953 and P . gingivalis ATCC 33277 (D) and P. gingivalis ATCC 33277 mono-species biofilm (E). Heat-killed F. nucleatum was boiled at 100 ° C for 1 h before being added to P . gingivalis ATCC 33277 biofilm.

    Article Snippet: The purified bacteriophage particles were visualised using a JEOL JEM−2100 transmission electron microscope (TEM) with 400-mesh carbon-coated copper grids (ProSciTech, Australia).

    Techniques: Confocal Microscopy, Cell Culture, Disruption