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virus atcc cat  (ATCC)


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    ATCC virus atcc cat
    Virus Atcc Cat, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 57 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/virus atcc cat/product/ATCC
    Average 93 stars, based on 57 article reviews
    virus atcc cat - by Bioz Stars, 2026-02
    93/100 stars

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    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.
    Reference Strains Atcc 49247, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.
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    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.
    Virus Strains Influenza A Virus H1n1 A Pr 8 34 Atcc, 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
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    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.
    Control Strain Atcc 49247, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC influenzae atcc 49247
    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.
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    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.

    Journal: bioRxiv

    Article Title: Tracking eco-evolutionary dynamics among lung pathobiome members from children with cystic fibrosis

    doi: 10.64898/2026.01.29.702708

    Figure Lengend Snippet: (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.

    Article Snippet: When comparing the IC 90 values for ampicillin and piperacillin–tazobactam to the reference strains ATCC 49247 (β-lactamase positive ) and ATCC 10211 (β-lactamase negative ), we observed that isolates covered the entire IC 90 space between the two references.

    Techniques: Sequencing, Activity Assay, Azocasein Assay, Concentration Assay, Crystal Violet Assay

    (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.

    Journal: bioRxiv

    Article Title: Tracking eco-evolutionary dynamics among lung pathobiome members from children with cystic fibrosis

    doi: 10.64898/2026.01.29.702708

    Figure Lengend Snippet: (A) Phylogenetic tree based on 1196 core genes of clinical H. influenzae isolates and three well-studied laboratory strains (86-028NP, ATCC 10211, and ATCC 49247). The table displays the ID of people with CF (pwCF) and the capsule presence (typeable vs non-typeable). Note that one isolate had to be excluded from genetic analysis due to poor sequence qualities. (B) Genome size (in base pairs) of the clinical isolates, grouped by time window. (C) Average genome composition of clinical isolates, with genes classified as core (present in 100% of isolates), soft-core (90–99%), shell (15–89%), and cloud (0–14%). (D) Protease activity of clinical isolates measured using the azocasein assay. (E) Siderophore production of clinical isolates measured using the chrome azurol S (CAS) assay in ssBHI medium supplemented with 2,2’-bipyridine to a final concentration of 75 μM. (F) Biofilm formation under static growth conditions measured using the crystal violet assay. Asterisks denote significance levels: ***P < 0.001; **P < 0.01; *P < 0.05.

    Article Snippet: Furthermore, we used laboratory strains, including P. aeruginosa PAO1 (ATCC 15692), S. aureus strains USA300 JE2 (ATCC-BAA-1717), Cowan 1 (ATCC 12598), and 6850 (ATCC 53657), and H. influenzae strains ATCC 49766 (NTHI), ATCC 49247 (NTHI) and ATCC 10211 (Serovar B) (Table S4).

    Techniques: Sequencing, Activity Assay, Azocasein Assay, Concentration Assay, Crystal Violet Assay