Review



ml  (Worthington Biochemical)


Bioz Verified Symbol Worthington Biochemical is a verified supplier
Bioz Manufacturer Symbol Worthington Biochemical manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • 99
      Buy from Supplier

    Structured Review

    Worthington Biochemical ml
    Ml, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/ml/custom%40ml%4042853924
    Average 99 stars, based on 1 article reviews
    ml - by Bioz Stars, 2026-10
    99/100 stars

    Images

    Related Articles

    Tissue:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Gentle:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Suspension:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Saline:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Analysis:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    FACS:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Single Cell:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Virus Isolation Assay:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Isolation:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Infection:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Adsorption:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Virus:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Flow Cytometry:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Cytometry:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Incubation:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Oligomer Restriction:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30

    Mouse Assay:

    Article Title: Correlative and Live-Cell Imaging of S100B-Promoter-Associated Interstitial Cells from the Cardiac Sinoatrial Node and Valves.
    Article Snippet: NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 5 HEPES, and 5.5 glucose (pH 7.0) for 10 min at 35 degrees C. They were then digested in 3 mL Ca2+-free Tyrode solution containing lyophilized elastase (2.0 mg; Worthington Biochemical, Lakewood, NJ, USA), protease (0.4 mg; Sigma- Aldrich, Burlington, MA, USA), collagenase type II (3 mg; Worthington Biochemical), and bovine serum albumin (3 mg; Sigma) for 30



    Similar Products

    nutristem hpsc xf with +20% ng/ml bfgf  (Polyplus-transfection SA)
    96
    Polyplus-transfection SA nutristem hpsc xf with +20% ng/ml bfgf
    Nutristem Hpsc Xf With +20% Ng/Ml Bfgf, supplied by Polyplus-transfection SA, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/NutriStem+hPSC+XF+with+%2B20%25+ng%2FmL+bFGF/polyplus-transfection+sa___06-5100-11-1a
    Average 96 stars, based on 1 article reviews
    nutristem hpsc xf with +20% ng/ml bfgf - by Bioz Stars, 2026-10
    96/100 stars
    		  Buy from Supplier
    ml  (Worthington Biochemical)
    99
    Worthington Biochemical ml
    Ml, supplied by Worthington Biochemical, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/ml/custom%40ml%4042882460
    Average 99 stars, based on 1 article reviews
    ml - by Bioz Stars, 2026-10
    99/100 stars
    		  Buy from Supplier
    cell strainers  (Greiner Bio)
    96
    Greiner Bio cell strainers
    Cell Strainers, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Easystrainer+70+%CE%9Cm+For+50+Ml+Tubes/pmc13676164-80-8-12
    Average 96 stars, based on 1 article reviews
    cell strainers - by Bioz Stars, 2026-10
    96/100 stars
    		  Buy from Supplier
    ml133  (Tocris)
    92
    Tocris ml133
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    Ml133, supplied by Tocris, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/ML+133+hydrochloride/pmc13673283-236-35-42
    Average 92 stars, based on 1 article reviews
    ml133 - by Bioz Stars, 2026-10
    92/100 stars
    		  Buy from Supplier
    liver pieces  (Santa Cruz Biotechnology)
    97
    Santa Cruz Biotechnology liver pieces
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    Liver Pieces, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Phosphate+Buffered+Saline/pm42888028-315-17-34
    Average 97 stars, based on 1 article reviews
    liver pieces - by Bioz Stars, 2026-10
    97/100 stars
    		  Buy from Supplier
    leucosep polypropylene tubes  (Greiner Bio)
    94
    Greiner Bio leucosep polypropylene tubes
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    Leucosep Polypropylene Tubes, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Leucosep+Tube+12+Ml+Pp+168%2F100+Mm/pm42882478-42-17-20
    Average 94 stars, based on 1 article reviews
    leucosep polypropylene tubes - by Bioz Stars, 2026-10
    94/100 stars
    		  Buy from Supplier
    leucosep tubes  (Greiner Bio)
    96
    Greiner Bio leucosep tubes
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    Leucosep Tubes, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Leucosep+Tube+50+Ml+Pp+30%2F115+Mm/pm42880372-46-23-26
    Average 96 stars, based on 1 article reviews
    leucosep tubes - by Bioz Stars, 2026-10
    96/100 stars
    		  Buy from Supplier
    k3edta plasma tubes  (Greiner Bio)
    93
    Greiner Bio k3edta plasma tubes
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    K3edta Plasma Tubes, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Vacuette+Tube+9+Ml+K3E+K3Edta/pm42880206-51-18-24
    Average 93 stars, based on 1 article reviews
    k3edta plasma tubes - by Bioz Stars, 2026-10
    93/100 stars
    		  Buy from Supplier
    master block  (Greiner Bio)
    95
    Greiner Bio master block
    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L <t>ML133</t> ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.
    Master Block, supplied by Greiner Bio, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml/Masterblock+96+Well+2+Ml+Pp+V-Bottom/pmc13635745-104-16-18
    Average 95 stars, based on 1 article reviews
    master block - by Bioz Stars, 2026-10
    95/100 stars
    		  Buy from Supplier

    Image Search Results


    Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L ML133 ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.

    Journal: Archiv Der Pharmazie

    Article Title: K + Channels in Membrane Potential Dynamics and Migration of Neutrophil Granulocytes

    doi: 10.1002/ardp.70365

    Figure Lengend Snippet: Membrane potential and migration velocity of C5a‐stimulated neutrophils in the absence and presence of different K + channel inhibitors. Neutrophils were always stimulated with 6 nmol/L C5a at t = 0 min. K + channel inhibitors were present throughout the entire experiment as indicated. The thin grey lines in panels A, C, E and G represent the mean values of neutrophils isolated from individual mice. The thick black lines illustrate the mean values derived from all individual mice. The mean values plotted in panels B, D, F and H were obtained from the time periods labeled by the shaded areas in panels A, C, E, and G. Rest., Peak and Repol. correspond to t = −3–0 min, maximal depolarization and t = 8–10 min, respectively. (A,B) Control experiments in the absence of K + channel inhibitors ( N = 12 mice; n = 135 cells; n ≥ 5 cells each). (C, D) Inhibition of K Ca 3.1 channels with 10 µmol/L senicapoc ( N = 4 mice; n = 40 cells; n ≥ 9 cells each). (E, F) Inhibition of K V 1.3 channels with Vm24 ( N = 4 mice; n = 42 cells; n ≥ 10 cells each). (G, H) Inhibition of K ir 2.1 channels with 10 µmol/L ML133 ( N = 3 mice; n = 34 cells; n ≥ 10 cells each). Normally distributed data were analyzed with one‐way ANOVA followed by Tukey's multiple comparison.

    Article Snippet: When indicated, we added either senicapoc (K Ca 3.1 inhibitor; 10 μM, kindly provided by Christina Kick, Institut für Pharmazeutische und Medizinische Chemie, University Münster), Vm24 (K V 1.3 inhibitor; 10 nM [ ]) or ML133 (K ir 2.1 inhibitor; 10 μM, Tocris Bioscience, UK) to the Ringer's solution.

    Techniques: Membrane, Migration, Isolation, Derivative Assay, Labeling, Control, Inhibition, Comparison

    Summary of key parameters obtained from the mathematical model analysis. The para meters are calculated for the movement into the direction of the C5a gradient (Y coordinate).

    Journal: Archiv Der Pharmazie

    Article Title: K + Channels in Membrane Potential Dynamics and Migration of Neutrophil Granulocytes

    doi: 10.1002/ardp.70365

    Figure Lengend Snippet: Summary of key parameters obtained from the mathematical model analysis. The para meters are calculated for the movement into the direction of the C5a gradient (Y coordinate).

    Article Snippet: When indicated, we added either senicapoc (K Ca 3.1 inhibitor; 10 μM, kindly provided by Christina Kick, Institut für Pharmazeutische und Medizinische Chemie, University Münster), Vm24 (K V 1.3 inhibitor; 10 nM [ ]) or ML133 (K ir 2.1 inhibitor; 10 μM, Tocris Bioscience, UK) to the Ringer's solution.

    Techniques: Analysis