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reference strains atcc 49247  (ATCC)


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    ATCC reference strains 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.
    Reference Strains Atcc 49247, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 799 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 799 article reviews
    reference strains atcc 49247 - by Bioz Stars, 2026-02
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    1) Product Images from "Tracking eco-evolutionary dynamics among lung pathobiome members from children with cystic fibrosis"

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

    Journal: bioRxiv

    doi: 10.64898/2026.01.29.702708

    (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.
    Figure Legend 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.

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



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    ATCC reference strains 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.
    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.
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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.
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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.
    Hi 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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    Image Search Results


    (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