96 well applied biosystem micro amp fast optical reaction plate Search Results


3730 xl 96 capillary dna analyzer  (Thermo Fisher)
99
Thermo Fisher 3730 xl 96 capillary dna analyzer
3730 Xl 96 Capillary Dna Analyzer, supplied by Thermo Fisher, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/DNA/pmc11432530-91-15-20
Average 99 stars, based on 1 article reviews
3730 xl 96 capillary dna analyzer - by Bioz Stars, 2026-09
99/100 stars
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96 well veritas luminometer  (Promega)
90
Promega 96 well veritas luminometer
96 Well Veritas Luminometer, supplied by Promega, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/glomax+20+20+luminometer/us09359635-597-16-18
Average 90 stars, based on 1 article reviews
96 well veritas luminometer - by Bioz Stars, 2026-09
90/100 stars
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fluorescent plate reader cytofluor 4000  (PerSeptive Biosystems Inc)
90
PerSeptive Biosystems Inc fluorescent plate reader cytofluor 4000
Fluorescent Plate Reader Cytofluor 4000, supplied by PerSeptive Biosystems Inc, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/cytofluor+multiwell+plate+reader/pm12181743-159-13-15
Average 90 stars, based on 1 article reviews
fluorescent plate reader cytofluor 4000 - by Bioz Stars, 2026-09
90/100 stars
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droparray 96 plate for bio-plextm  (Curiox Biosystems)
90
Curiox Biosystems droparray 96 plate for bio-plextm
Droparray 96 Plate For Bio Plextm, supplied by Curiox Biosystems, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/droparray++384+well+cell+plate/pmc06602177-109-14-19
Average 90 stars, based on 1 article reviews
droparray 96 plate for bio-plextm - by Bioz Stars, 2026-09
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cytoview mea plate  (Axion BioSystems)
90
Axion BioSystems cytoview mea plate
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
Cytoview Mea Plate, supplied by Axion BioSystems, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/cytoview+mea+24+well+plates/pmc07571425-97-8-13
Average 90 stars, based on 1 article reviews
cytoview mea plate - by Bioz Stars, 2026-09
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celltiter 96® aqueous nonradioactive cell proliferation assay kit  (Promega)
90
Promega celltiter 96® aqueous nonradioactive cell proliferation assay kit
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
Celltiter 96® Aqueous Nonradioactive Cell Proliferation Assay Kit, supplied by Promega, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/celltiter+glo+luminescent+cell+viability+assay/pmc03937249-66-27-40
Average 90 stars, based on 1 article reviews
celltiter 96® aqueous nonradioactive cell proliferation assay kit - by Bioz Stars, 2026-09
90/100 stars
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384 well plate  (Thermo Fisher)
99
Thermo Fisher 384 well plate
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
384 Well Plate, supplied by Thermo Fisher, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/Ampicillin+trihydrate/pmc05622443-82-7-23
Average 99 stars, based on 1 article reviews
384 well plate - by Bioz Stars, 2026-09
99/100 stars
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cfx 96  (Bio-Rad)
99
Bio-Rad cfx 96
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
Cfx 96, 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
https://www.bioz.com/product/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/CFX96+and+CFX384+Real-Time+PCR+Detection+Systems+Firmware+Update/pmc10388288__2022_281955_ZHANG_SUPPL-41-16-20
Average 99 stars, based on 1 article reviews
cfx 96 - by Bioz Stars, 2026-09
99/100 stars
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6 carboxyfluorescein fam  (Thermo Fisher)
94
Thermo Fisher 6 carboxyfluorescein fam
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
6 Carboxyfluorescein Fam, supplied by Thermo Fisher, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/6-Carboxyfluorescein%2C+96%25/pmc06638359-436-9-22
Average 94 stars, based on 1 article reviews
6 carboxyfluorescein fam - by Bioz Stars, 2026-09
94/100 stars
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cytoview-z  (Axion BioSystems)
90
Axion BioSystems cytoview-z
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
Cytoview Z, supplied by Axion BioSystems, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/cytoview+z+96+well+plates/pm37820720-294-16-23
Average 90 stars, based on 1 article reviews
cytoview-z - by Bioz Stars, 2026-09
90/100 stars
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96-well sru bindtm streptavidin-coated plates  (SRU Biosystems)
90
SRU Biosystems 96-well sru bindtm streptavidin-coated plates
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
96 Well Sru Bindtm Streptavidin Coated Plates, supplied by SRU Biosystems, 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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Average 90 stars, based on 1 article reviews
96-well sru bindtm streptavidin-coated plates - by Bioz Stars, 2026-09
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laminar wash 96-well plate  (Curiox Biosystems)
90
Curiox Biosystems laminar wash 96-well plate
Characterization of cardiomyocytes-derived from human pluripotent stem <t>cells</t> <t>(hPSC-CMs).</t> (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array <t>(MEA)</t> system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).
Laminar Wash 96 Well Plate, supplied by Curiox Biosystems, 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/96+well+applied+biosystem+micro+amp+fast+optical+reaction+plate/laminar+wash+96+well+plate/pm33336868-41-45-49
Average 90 stars, based on 1 article reviews
laminar wash 96-well plate - by Bioz Stars, 2026-09
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Image Search Results


Characterization of cardiomyocytes-derived from human pluripotent stem cells (hPSC-CMs). (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array (MEA) system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).

Journal: Antiviral Research

Article Title: Antiviral activity and safety of remdesivir against SARS-CoV-2 infection in human pluripotent stem cell-derived cardiomyocytes

doi: 10.1016/j.antiviral.2020.104955

Figure Lengend Snippet: Characterization of cardiomyocytes-derived from human pluripotent stem cells (hPSC-CMs). (A) Schematic diagram of hPSC differentiation into cardiomyocytes. (B) The morphology of differentiated hPSC-CMs derived from two hPSC cell lines (hESCs: H9 and hiPSCs: CMC-11; 10 × magnification). (C) The RT-qPCR was performed to measure the expression of cardiac sarcomeric markers, cTnT, and MYH6 genes, in hPSC-CMs. The data represent the mean (±SD) of at least two independent experiments performed in triplicate. Statistical analyses were determined using paired student's t -tests, and P < 0.05 was considered as significant (*). (D) Expression of TNNT2 and ACTN2 in hPSC-CMs (hESC-CMs [upper panel] and hiPSC-CMs [lower panel]) at day 15 of differentiation were determined by flow cytometry and immunofluorescence analyses. Scale bar, 100 μm. (E) Beating cardiomyocytes were prepared for action potential (AP) recording using the patch-clamp technique in hESC-CMs and field potential (FP) recording using a multielectrode array (MEA) system in hiPSC-CMs. The hPSC-CMs were treated with 100 nM isoprenaline (β 2 -adrenergic receptor agonist), 0.3 μM and 1 μM nifedipine (L-type Ca 2+ channel blocker), and 10 nM dofetilide and 30 nM E4031 (hERG K + channel blockers).

Article Snippet: For MEA analysis, hPSC-CMs were seeded on 96-well MEA plates (Cytoview MEA plate, Axion BioSystems, USA) prior to drug treatment.

Techniques: Derivative Assay, Quantitative RT-PCR, Expressing, Flow Cytometry, Immunofluorescence, Patch Clamp