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bal protein level  (Bio-Rad)


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    Structured Review

    Bio-Rad bal protein level
    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and <t>BAL</t> were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c <t>),</t> <t>acellular</t> BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).
    Bal Protein Level, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 44837 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bal protein level/product/Bio-Rad
    Average 99 stars, based on 44837 article reviews
    bal protein level - by Bioz Stars, 2026-05
    99/100 stars

    Images

    1) Product Images from "Concentrated Secretome of Adipose Stromal Cells Limits Influenza A Virus-Induced Lung Injury in Mice"

    Article Title: Concentrated Secretome of Adipose Stromal Cells Limits Influenza A Virus-Induced Lung Injury in Mice

    Journal: Cells

    doi: 10.3390/cells10040720

    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and BAL were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).
    Figure Legend Snippet: Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and BAL were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).

    Techniques Used: Infection, Cell Counting, Control, Saline

    ASC-CS administration limits BAL protein and inflammatory cell extravasation, and increases in granzyme B and MPO without compromise of viral clearance in IAV-infected mice. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Mice receiving vehicle control for IAV are annotated as saline (sal, black columns). On Day6 and 8, IAV mice were sub-cutaneously injected with 2.25 mg/kg of ASC-CS (CS, green columns) or an equivalent volume of PBS (red columns designated as IAV). Lungs and BAL were collected on Day9 to analyze for BAL white blood cell count ( a ) and total protein levels ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin (HA) level ( f ). n = 4–6 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between (1) IAV groups and the control group (vs. sal), and (2) CM groups and the corresponding gender IAV group (vs. IAV).
    Figure Legend Snippet: ASC-CS administration limits BAL protein and inflammatory cell extravasation, and increases in granzyme B and MPO without compromise of viral clearance in IAV-infected mice. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Mice receiving vehicle control for IAV are annotated as saline (sal, black columns). On Day6 and 8, IAV mice were sub-cutaneously injected with 2.25 mg/kg of ASC-CS (CS, green columns) or an equivalent volume of PBS (red columns designated as IAV). Lungs and BAL were collected on Day9 to analyze for BAL white blood cell count ( a ) and total protein levels ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin (HA) level ( f ). n = 4–6 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between (1) IAV groups and the control group (vs. sal), and (2) CM groups and the corresponding gender IAV group (vs. IAV).

    Techniques Used: Infection, Control, Saline, Injection, Cell Counting



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    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and <t>BAL</t> were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c <t>),</t> <t>acellular</t> BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).
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    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and <t>BAL</t> were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c <t>),</t> <t>acellular</t> BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).
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    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and <t>BAL</t> were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c <t>),</t> <t>acellular</t> BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).
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    Image Search Results


    Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and BAL were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).

    Journal: Cells

    Article Title: Concentrated Secretome of Adipose Stromal Cells Limits Influenza A Virus-Induced Lung Injury in Mice

    doi: 10.3390/cells10040720

    Figure Lengend Snippet: Murine lung infection with IAV is characterized by two distinct phases, a viral clearance phase and a lung injury phase, with white blood cell infiltration during former and latter phases. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Lungs and BAL were collected on the days indicated to analyze for BAL total protein levels ( a ) and white blood cell count ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin level ( f ). n = 4–8 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between IAV groups and the control group, receiving saline in lung (plotted as D0).

    Article Snippet: BAL protein level was measured in acellular BAL using Bradford assay (BioRad, Hercules, CA, USA).

    Techniques: Infection, Cell Counting, Control, Saline

    ASC-CS administration limits BAL protein and inflammatory cell extravasation, and increases in granzyme B and MPO without compromise of viral clearance in IAV-infected mice. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Mice receiving vehicle control for IAV are annotated as saline (sal, black columns). On Day6 and 8, IAV mice were sub-cutaneously injected with 2.25 mg/kg of ASC-CS (CS, green columns) or an equivalent volume of PBS (red columns designated as IAV). Lungs and BAL were collected on Day9 to analyze for BAL white blood cell count ( a ) and total protein levels ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin (HA) level ( f ). n = 4–6 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between (1) IAV groups and the control group (vs. sal), and (2) CM groups and the corresponding gender IAV group (vs. IAV).

    Journal: Cells

    Article Title: Concentrated Secretome of Adipose Stromal Cells Limits Influenza A Virus-Induced Lung Injury in Mice

    doi: 10.3390/cells10040720

    Figure Lengend Snippet: ASC-CS administration limits BAL protein and inflammatory cell extravasation, and increases in granzyme B and MPO without compromise of viral clearance in IAV-infected mice. C57Bl/6 mice received intranasal administration of IAV H1N1 PR8 (800 pfu/mouse) on Day0. Mice receiving vehicle control for IAV are annotated as saline (sal, black columns). On Day6 and 8, IAV mice were sub-cutaneously injected with 2.25 mg/kg of ASC-CS (CS, green columns) or an equivalent volume of PBS (red columns designated as IAV). Lungs and BAL were collected on Day9 to analyze for BAL white blood cell count ( a ) and total protein levels ( b ), lung wet/dry ratio ( c ), acellular BAL granzyme B ( d ) and MPO ( e ) levels, and PR8 hemagglutinin (HA) level ( f ). n = 4–6 per group, presented are mean +/− SEM. * for p < 0.05 by t -test with Welch correction (unequal variances) between (1) IAV groups and the control group (vs. sal), and (2) CM groups and the corresponding gender IAV group (vs. IAV).

    Article Snippet: BAL protein level was measured in acellular BAL using Bradford assay (BioRad, Hercules, CA, USA).

    Techniques: Infection, Control, Saline, Injection, Cell Counting