calcein acetoxymethylester Search Results


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  • 99
    Thermo Fisher calcein acetoxymethylester calcein am
    Calcein Acetoxymethylester Calcein Am, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 37 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Becton Dickinson calcein acetoxymethylester fluorescent dye
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    Thermo Fisher calcein violet acetoxymethylester
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    Thermo Fisher calcein am cell permeant dye
    (A, B) Neuroprotective effects of Akt activation by odorant stimulation in the early stage. In the presence of 10 μM odorants, ORNs were co-incubated for 6 h in the presence or absence of (A) 50 μM LY294002 or (B) siRNA for Akt1, respectively. (C, D) Neuroprotective effects of Akt activation by odorant stimulation in the late stage. In the presence of 10 μM odorants, ORNs were co-incubated for 18 h in the presence or absence of (C) 50 μM LY294002 or (D) siRNA for Akt1, respectively. Cell viability was assessed by the <t>calcein</t> assay. Data are expressed as percent of value in untreated control cultures (serum free condition). Data are presented as means ± SEM from three independent experiments. One-way ANOVA, followed by Dunnett’s post hoc test, was performed. **P
    Calcein Am Cell Permeant Dye, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 150 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A, B) Neuroprotective effects of Akt activation by odorant stimulation in the early stage. In the presence of 10 μM odorants, ORNs were co-incubated for 6 h in the presence or absence of (A) 50 μM LY294002 or (B) siRNA for Akt1, respectively. (C, D) Neuroprotective effects of Akt activation by odorant stimulation in the late stage. In the presence of 10 μM odorants, ORNs were co-incubated for 18 h in the presence or absence of (C) 50 μM LY294002 or (D) siRNA for Akt1, respectively. Cell viability was assessed by the calcein assay. Data are expressed as percent of value in untreated control cultures (serum free condition). Data are presented as means ± SEM from three independent experiments. One-way ANOVA, followed by Dunnett’s post hoc test, was performed. **P

    Journal: Molecules and Cells

    Article Title: Odorant Stimulation Promotes Survival of Rodent Olfactory Receptor Neurons via PI3K/Akt Activation and Bcl-2 Expression

    doi: 10.14348/molcells.2015.0038

    Figure Lengend Snippet: (A, B) Neuroprotective effects of Akt activation by odorant stimulation in the early stage. In the presence of 10 μM odorants, ORNs were co-incubated for 6 h in the presence or absence of (A) 50 μM LY294002 or (B) siRNA for Akt1, respectively. (C, D) Neuroprotective effects of Akt activation by odorant stimulation in the late stage. In the presence of 10 μM odorants, ORNs were co-incubated for 18 h in the presence or absence of (C) 50 μM LY294002 or (D) siRNA for Akt1, respectively. Cell viability was assessed by the calcein assay. Data are expressed as percent of value in untreated control cultures (serum free condition). Data are presented as means ± SEM from three independent experiments. One-way ANOVA, followed by Dunnett’s post hoc test, was performed. **P

    Article Snippet: Cell viability assay Cell viability was monitored by the calcein assay, which examined cells stained with calcein acetoxymethylester (AM) (C3100MP, Invitrogen, USA).

    Techniques: Activation Assay, Incubation