(quantum fitc-5 mesf kit Search Results


annexin v fitc  (Beijing Solarbio Science)
97
Beijing Solarbio Science annexin v fitc
(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by <t>Annexin</t> V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.
Annexin V Fitc, supplied by Beijing Solarbio Science, 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/%28quantum+fitc-5+mesf+kit/pmc07967038-123-10-29?v=Beijing+Solarbio+Science
Average 97 stars, based on 1 article reviews
annexin v fitc - by Bioz Stars, 2026-08
97/100 stars
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fitc 5-bromo-20deoxyuridine (brdu) flow kit  (Becton Dickinson)
90
Becton Dickinson fitc 5-bromo-20deoxyuridine (brdu) flow kit
(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by <t>Annexin</t> V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.
Fitc 5 Bromo 20deoxyuridine (Brdu) Flow Kit, supplied by Becton Dickinson, 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/%28quantum+fitc-5+mesf+kit/pm21710478-154-1-6?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
fitc 5-bromo-20deoxyuridine (brdu) flow kit - by Bioz Stars, 2026-08
90/100 stars
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quantum fitc 5 mesf kit  (Bangs Laboratories)
86
Bangs Laboratories quantum fitc 5 mesf kit
(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by <t>Annexin</t> V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.
Quantum Fitc 5 Mesf Kit, supplied by Bangs Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/%28quantum+fitc-5+mesf+kit/pm26329844-193-16-20?v=Bangs+Laboratories
Average 86 stars, based on 1 article reviews
quantum fitc 5 mesf kit - by Bioz Stars, 2026-08
86/100 stars
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annexin v fitc  (Danaher Inc)
94
Danaher Inc annexin v fitc
(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by <t>Annexin</t> V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.
Annexin V Fitc, supplied by Danaher Inc, 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/%28quantum+fitc-5+mesf+kit/pmc03130899-330-23-27?v=Danaher+Inc
Average 94 stars, based on 1 article reviews
annexin v fitc - by Bioz Stars, 2026-08
94/100 stars
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5-bromo-20-deoxyuridine (brdurd) flow kit  (Becton Dickinson)
90
Becton Dickinson 5-bromo-20-deoxyuridine (brdurd) flow kit
(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by <t>Annexin</t> V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.
5 Bromo 20 Deoxyuridine (Brdurd) Flow Kit, supplied by Becton Dickinson, 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/%28quantum+fitc-5+mesf+kit/10__1158_slash_1541___7786__mcr___11___0508-57-6-13?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
5-bromo-20-deoxyuridine (brdurd) flow kit - by Bioz Stars, 2026-08
90/100 stars
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Image Search Results


(a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by Annexin V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.

Journal: Redox Biology

Article Title: Kaempferol alleviates LD-mitochondrial damage by promoting autophagy: Implications in Parkinson's disease

doi: 10.1016/j.redox.2021.101911

Figure Lengend Snippet: (a) Cell viability was measured in Ka-treated (0, 3, 30, 60, 100, 300, or 600 μM; 24 h) SH-SY5Y cells by CCK-8 assays. The chemical structure of Ka is shown under the curve. (b) LDH assays of SH-SY 5Y cells treated with Ka (3, 10, 30, or 60 μM) and/or MPP + (400 μM, 24 h). (c– e) Ka (30 μM)- and/or MPP + (400 μM)-treated SH-SY5Y cells were stained with Hoechst 33,342 and PI and then observed by fluorescence microscopy. Scale bars, 80 μm. Quantification of Hoechst-positive (d) and Hoechst/PI double-positive (e) cells was performed. (f–g) SH-SY5Y cells treated with Ka (30 μM)- and/or MPP + (400 μM) for 24 h, then apoptosis was assessed by Annexin V/PI staining and flow cytometry. The data for flow cytometry analysis are presented as a percentage of the cell population by normalizing to control samples. (h–k) Ka (30 μM)-pretreated SH-SY5Y cells were stimulated with or without MPP + (400 μM). Representative immunoblots (h) and quantitative analysis of Bcl-2, Bax, procaspase-3 and cleaved caspase-3 in cell extracts (i, j,k). The data are expressed as the mean ± SEM and are representative of at least three independent experiments. * P < 0.05, ** P < 0.01, *** P < 0.001, by one-way ANOVA followed by Tukey's post hoc test. Ka, kaempferol.

Article Snippet: Cells were digested and rinsed with D-hank's then stained with Annexin V-FITC (5 μl diluted in 500 μl PBS)/PI (0.1 μl diluted in 500 μl PBS) apoptosis kit (CA1020, Solarbio, Beijing, Chian) according to the manufacturer's protocol.

Techniques: CCK-8 Assay, Staining, Fluorescence, Microscopy, Flow Cytometry, Control, Western Blot