k. pneumoniae isolates Search Results


90
EPIRUS Inc ndm-1-producing k. pneumoniae isolate
Ndm 1 Producing K. Pneumoniae Isolate, supplied by EPIRUS Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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National Reference Center for Legionella clinical kpc-3 k. pneumoniae isolate nara864
Clinical Kpc 3 K. Pneumoniae Isolate Nara864, supplied by National Reference Center for Legionella, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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AstraZeneca ltd kpc-producing k. pneumoniae isolates
Kpc Producing K. Pneumoniae Isolates, supplied by AstraZeneca ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Parkwood Mennonite Home k . pneumoniae clinical isolate parkwood-18
Human peripheral blood mononuclear cells (PBMCs) ( n = 8) were left untreated or stimulated for 24 h with SEB. They were then washed and rested for 3 days before they were exposed to K . <t>pneumoniae</t> lysate. Interferon (IFN)-γ + , tumor necrosis factor (TNF)-α + , interleukin (IL)-2 + , and IL-17A + events among MAIT cells were enumerated 24 h later by intracellular cytokine staining ( A ). PBMCs from a separate cohort were subjected to SEB stimulation, followed by 24 h of resting, before they were challenged with either K . pneumoniae or E . coli lysate. Twenty-four hours later, cells were interrogated for their intracellular IFN-γ content ( n = 13) and evaluated for staining with Annexin V or Fixable Viability Dye ( n = 4) ( B ). SEB-exposed CD3 + cells co-expressing LAG-3 were divided into 5 subpopulations based on CD161 and Vα7.2 staining. The relative contribution of each subpopulation to total CD3/LAG-3 double-expressors is depicted in a pie chart generated using PBMCs from 8 donors ( C ). Concomitant upregulation of CD69 and LAG-3 by SEB, or lack thereof, was also examined in conventional T (T conv ) and MAIT cell compartments. Representative FACS plots are shown ( n = 8) ( D ). In additional experiments, the frequencies of LAG-3 + MAIT cells were determined in PBMC cultures containing 20 μM SB203580 or PD98059 ( E ), 5 ng/mL recombinant human IL-12 (rIL-12) and/or recombinant human IL-18 (rIL-18) ( F ), 5 μg/mL anti-IL-12 and anti-IL-18 ± 200 ng/mL cyclosporine A (CsA) ( n = 3) ( G ). The proportions of LAG-3 + TIM-3 - and LAG-3/TIM-3 double-expressors among T conv and MAIT cells were also calculated at indicated time points after SEB stimulation of PBMCs ( n = 8) ( H ). In separate experiments, PBMC cultures were stimulated for 24 h with SEB. Cells were washed, and cultures were replenished with fresh medium containing 20 μg/mL of an anti-human LAG-3 monoclonal antibody (mAb) or a mouse IgG1 isotype control. Klebsiella lysate was added to cultures, followed, 24 h later, by enumeration of IFN-γ + MAIT cells ( n = 3) ( I ). Error bars represent SEM. The underlying data for this figure can be found in , and our gating strategies are provided in .
K . Pneumoniae Clinical Isolate Parkwood 18, supplied by Parkwood Mennonite Home, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/k%2E+pneumoniae+isolates/pmc05478099-353-7-10?v=Parkwood+Mennonite+Home
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k . pneumoniae clinical isolate parkwood-18 - by Bioz Stars, 2026-08
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90
National Reference Center for Legionella k. pneumoniae isolates ff and um
Human peripheral blood mononuclear cells (PBMCs) ( n = 8) were left untreated or stimulated for 24 h with SEB. They were then washed and rested for 3 days before they were exposed to K . <t>pneumoniae</t> lysate. Interferon (IFN)-γ + , tumor necrosis factor (TNF)-α + , interleukin (IL)-2 + , and IL-17A + events among MAIT cells were enumerated 24 h later by intracellular cytokine staining ( A ). PBMCs from a separate cohort were subjected to SEB stimulation, followed by 24 h of resting, before they were challenged with either K . pneumoniae or E . coli lysate. Twenty-four hours later, cells were interrogated for their intracellular IFN-γ content ( n = 13) and evaluated for staining with Annexin V or Fixable Viability Dye ( n = 4) ( B ). SEB-exposed CD3 + cells co-expressing LAG-3 were divided into 5 subpopulations based on CD161 and Vα7.2 staining. The relative contribution of each subpopulation to total CD3/LAG-3 double-expressors is depicted in a pie chart generated using PBMCs from 8 donors ( C ). Concomitant upregulation of CD69 and LAG-3 by SEB, or lack thereof, was also examined in conventional T (T conv ) and MAIT cell compartments. Representative FACS plots are shown ( n = 8) ( D ). In additional experiments, the frequencies of LAG-3 + MAIT cells were determined in PBMC cultures containing 20 μM SB203580 or PD98059 ( E ), 5 ng/mL recombinant human IL-12 (rIL-12) and/or recombinant human IL-18 (rIL-18) ( F ), 5 μg/mL anti-IL-12 and anti-IL-18 ± 200 ng/mL cyclosporine A (CsA) ( n = 3) ( G ). The proportions of LAG-3 + TIM-3 - and LAG-3/TIM-3 double-expressors among T conv and MAIT cells were also calculated at indicated time points after SEB stimulation of PBMCs ( n = 8) ( H ). In separate experiments, PBMC cultures were stimulated for 24 h with SEB. Cells were washed, and cultures were replenished with fresh medium containing 20 μg/mL of an anti-human LAG-3 monoclonal antibody (mAb) or a mouse IgG1 isotype control. Klebsiella lysate was added to cultures, followed, 24 h later, by enumeration of IFN-γ + MAIT cells ( n = 3) ( I ). Error bars represent SEM. The underlying data for this figure can be found in , and our gating strategies are provided in .
K. Pneumoniae Isolates Ff And Um, supplied by National Reference Center for Legionella, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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k. pneumoniae isolates ff and um - by Bioz Stars, 2026-08
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90
IDEXX presumptive k. pneumoniae isolates
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
Presumptive K. Pneumoniae Isolates, supplied by IDEXX, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Wyeth Ayerst Laboratories ampc positive isolate of k. pneumoniae
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
Ampc Positive Isolate Of K. Pneumoniae, supplied by Wyeth Ayerst Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ANSES laboratories non-duplicate k. pneumoniae isolates
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
Non Duplicate K. Pneumoniae Isolates, supplied by ANSES laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MBL Life science mbl-producing k. pneumoniae 1.41 isolate
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
Mbl Producing K. Pneumoniae 1.41 Isolate, supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Meridian HealthComms mbl-producing k. pneumoniae isolates
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
Mbl Producing K. Pneumoniae Isolates, supplied by Meridian HealthComms, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MBL Life science k. pneumoniae strains isolated in 2012 from two colonized children (stool samples/rectal swabs)
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
K. Pneumoniae Strains Isolated In 2012 From Two Colonized Children (Stool Samples/Rectal Swabs), supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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k. pneumoniae strains isolated in 2012 from two colonized children (stool samples/rectal swabs) - by Bioz Stars, 2026-08
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MedImmune llc k. pneumoniae isolates
Host, source, and MLST diversity of 53 <t> K. pneumoniae </t> / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.
K. Pneumoniae Isolates, supplied by MedImmune llc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Human peripheral blood mononuclear cells (PBMCs) ( n = 8) were left untreated or stimulated for 24 h with SEB. They were then washed and rested for 3 days before they were exposed to K . pneumoniae lysate. Interferon (IFN)-γ + , tumor necrosis factor (TNF)-α + , interleukin (IL)-2 + , and IL-17A + events among MAIT cells were enumerated 24 h later by intracellular cytokine staining ( A ). PBMCs from a separate cohort were subjected to SEB stimulation, followed by 24 h of resting, before they were challenged with either K . pneumoniae or E . coli lysate. Twenty-four hours later, cells were interrogated for their intracellular IFN-γ content ( n = 13) and evaluated for staining with Annexin V or Fixable Viability Dye ( n = 4) ( B ). SEB-exposed CD3 + cells co-expressing LAG-3 were divided into 5 subpopulations based on CD161 and Vα7.2 staining. The relative contribution of each subpopulation to total CD3/LAG-3 double-expressors is depicted in a pie chart generated using PBMCs from 8 donors ( C ). Concomitant upregulation of CD69 and LAG-3 by SEB, or lack thereof, was also examined in conventional T (T conv ) and MAIT cell compartments. Representative FACS plots are shown ( n = 8) ( D ). In additional experiments, the frequencies of LAG-3 + MAIT cells were determined in PBMC cultures containing 20 μM SB203580 or PD98059 ( E ), 5 ng/mL recombinant human IL-12 (rIL-12) and/or recombinant human IL-18 (rIL-18) ( F ), 5 μg/mL anti-IL-12 and anti-IL-18 ± 200 ng/mL cyclosporine A (CsA) ( n = 3) ( G ). The proportions of LAG-3 + TIM-3 - and LAG-3/TIM-3 double-expressors among T conv and MAIT cells were also calculated at indicated time points after SEB stimulation of PBMCs ( n = 8) ( H ). In separate experiments, PBMC cultures were stimulated for 24 h with SEB. Cells were washed, and cultures were replenished with fresh medium containing 20 μg/mL of an anti-human LAG-3 monoclonal antibody (mAb) or a mouse IgG1 isotype control. Klebsiella lysate was added to cultures, followed, 24 h later, by enumeration of IFN-γ + MAIT cells ( n = 3) ( I ). Error bars represent SEM. The underlying data for this figure can be found in , and our gating strategies are provided in .

Journal: PLoS Biology

Article Title: MAIT cells launch a rapid, robust and distinct hyperinflammatory response to bacterial superantigens and quickly acquire an anergic phenotype that impedes their cognate antimicrobial function: Defining a novel mechanism of superantigen-induced immunopathology and immunosuppression

doi: 10.1371/journal.pbio.2001930

Figure Lengend Snippet: Human peripheral blood mononuclear cells (PBMCs) ( n = 8) were left untreated or stimulated for 24 h with SEB. They were then washed and rested for 3 days before they were exposed to K . pneumoniae lysate. Interferon (IFN)-γ + , tumor necrosis factor (TNF)-α + , interleukin (IL)-2 + , and IL-17A + events among MAIT cells were enumerated 24 h later by intracellular cytokine staining ( A ). PBMCs from a separate cohort were subjected to SEB stimulation, followed by 24 h of resting, before they were challenged with either K . pneumoniae or E . coli lysate. Twenty-four hours later, cells were interrogated for their intracellular IFN-γ content ( n = 13) and evaluated for staining with Annexin V or Fixable Viability Dye ( n = 4) ( B ). SEB-exposed CD3 + cells co-expressing LAG-3 were divided into 5 subpopulations based on CD161 and Vα7.2 staining. The relative contribution of each subpopulation to total CD3/LAG-3 double-expressors is depicted in a pie chart generated using PBMCs from 8 donors ( C ). Concomitant upregulation of CD69 and LAG-3 by SEB, or lack thereof, was also examined in conventional T (T conv ) and MAIT cell compartments. Representative FACS plots are shown ( n = 8) ( D ). In additional experiments, the frequencies of LAG-3 + MAIT cells were determined in PBMC cultures containing 20 μM SB203580 or PD98059 ( E ), 5 ng/mL recombinant human IL-12 (rIL-12) and/or recombinant human IL-18 (rIL-18) ( F ), 5 μg/mL anti-IL-12 and anti-IL-18 ± 200 ng/mL cyclosporine A (CsA) ( n = 3) ( G ). The proportions of LAG-3 + TIM-3 - and LAG-3/TIM-3 double-expressors among T conv and MAIT cells were also calculated at indicated time points after SEB stimulation of PBMCs ( n = 8) ( H ). In separate experiments, PBMC cultures were stimulated for 24 h with SEB. Cells were washed, and cultures were replenished with fresh medium containing 20 μg/mL of an anti-human LAG-3 monoclonal antibody (mAb) or a mouse IgG1 isotype control. Klebsiella lysate was added to cultures, followed, 24 h later, by enumeration of IFN-γ + MAIT cells ( n = 3) ( I ). Error bars represent SEM. The underlying data for this figure can be found in , and our gating strategies are provided in .

Article Snippet: A frozen stock of a K . pneumoniae clinical isolate, Parkwood-18, was a gift from Dr. Miguel Valvano (Queen’s University Belfast, Belfast, United Kingdom).

Techniques: Staining, Expressing, Generated, Recombinant, Control

Host, source, and MLST diversity of 53  K. pneumoniae  / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.

Journal: Pathogens

Article Title: Molecular Characterization of Presumptive Klebsiella pneumoniae Isolates from Companion and Farm Animals in Germany Reveals Novel Sequence Types

doi: 10.3390/pathogens14030259

Figure Lengend Snippet: Host, source, and MLST diversity of 53 K. pneumoniae / quasipneumoniae strains with 46 distinct STs obtained from various companion and farm animals in Germany in 2023.

Article Snippet: Sixty-four presumptive K. pneumoniae isolates from the strain collection of IDEXX Laboratories, Kornwestheim, Germany, were used in the current study.

Techniques:

The phylogenetic tree of 64 K. pneumoniae / quasipneumoniae isolates from companion and farm animals in Germany was constructed using the Neighbor-Joining (NJ) method based on MLST data. The tree includes STs and corresponding geographical locations. Novel STs are indicated in red.

Journal: Pathogens

Article Title: Molecular Characterization of Presumptive Klebsiella pneumoniae Isolates from Companion and Farm Animals in Germany Reveals Novel Sequence Types

doi: 10.3390/pathogens14030259

Figure Lengend Snippet: The phylogenetic tree of 64 K. pneumoniae / quasipneumoniae isolates from companion and farm animals in Germany was constructed using the Neighbor-Joining (NJ) method based on MLST data. The tree includes STs and corresponding geographical locations. Novel STs are indicated in red.

Article Snippet: Sixty-four presumptive K. pneumoniae isolates from the strain collection of IDEXX Laboratories, Kornwestheim, Germany, were used in the current study.

Techniques: Construct

MLST characteristics of the eleven  K. pneumoniae  / quasipneumoniae isolates with novel STs obtained from companion and farm animals in Germany in 2023.

Journal: Pathogens

Article Title: Molecular Characterization of Presumptive Klebsiella pneumoniae Isolates from Companion and Farm Animals in Germany Reveals Novel Sequence Types

doi: 10.3390/pathogens14030259

Figure Lengend Snippet: MLST characteristics of the eleven K. pneumoniae / quasipneumoniae isolates with novel STs obtained from companion and farm animals in Germany in 2023.

Article Snippet: Sixty-four presumptive K. pneumoniae isolates from the strain collection of IDEXX Laboratories, Kornwestheim, Germany, were used in the current study.

Techniques: