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Benchmark Plus Microplate Reader, supplied by Bio-Rad, 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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BMG Labtech multi-mode microplate reader clariostar plus
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Multi Mode Microplate Reader Clariostar Plus, supplied by BMG Labtech, 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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Hidex microplate reader hidex sense beta plus type 425-311
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Microplate Reader Hidex Sense Beta Plus Type 425 311, supplied by Hidex, 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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BMG Labtech microplate reader clariostar plus
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Microplate Reader Clariostar Plus, supplied by BMG Labtech, 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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Greiner Bio clariostar® plus microplate reader
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Clariostar® Plus Microplate Reader, supplied by Greiner Bio, 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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BMG Labtech plate reader clariostar plus microplate
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Plate Reader Clariostar Plus Microplate, supplied by BMG Labtech, 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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BMG Labtech clariostar plus microplate reader
Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence <t>microplate</t> reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.
Clariostar Plus Microplate Reader, supplied by BMG Labtech, 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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Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence microplate reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.

Journal: Biochemistry and Biophysics Reports

Article Title: Antimicrobial peptide LL-37 increases rhinovirus-induced interferon β expression in human airway epithelial cells through a Ca 2+ -dependent mechanism

doi: 10.1016/j.bbrep.2025.102105

Figure Lengend Snippet: Stimulation with LL-37 increases intracellular Ca 2+ concentration in BEAS-2B cells. (A, B) Cells were loaded with the fluorescent Ca 2+ indicator dye Fluo-4 AM and stimulated with or without LL-37 (4 μM) in Ca 2+ -containing (2.5 mM) HEPES solution. ( A ) Fluorescence was assessed continuously every 5 min for 40 min in a fluorescence microplate reader, and the time curve plotted and normalized to background fluorescence before LL-37 or vehicle was introduced. ( B ) Fluorescence determined at the endpoint (40 min) and compared to vehicle control. The fluorescence signal was normalized to fluorescence in control cells for each of the 4 independent experiments. DMSO (0.1 %) was included as vehicle control. Values are presented as means ± SEM. ∗ represents P < 0.05 vs. vehicle control determined with Student’s two-tailed unpaired t -test for single comparisons between two groups as appropriate.

Article Snippet: Cells were treated with LL-37 (4 μM) or vehicle in HEPES solution with a physiological concentration of Ca 2+ (2.5 mM), and cellular fluorescence determined in a CLARIOstar Plus multi-mode microplate reader (BMG Labtech).

Techniques: Concentration Assay, Fluorescence, Control, Two Tailed Test