live dead staining Search Results


93
Biotium ab181421 yeast live
Ab181421 Yeast Live, supplied by Biotium, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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Beyotime dead bacterial staining kit
Dead Bacterial Staining Kit, supplied by Beyotime, 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/live+dead+staining/pmc12205665-35-6-18?v=Beyotime
Average 99 stars, based on 1 article reviews
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92
ImmunoChemistry Technologies aad red fluorescent live
Aad Red Fluorescent Live, supplied by ImmunoChemistry Technologies, 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/live+dead+staining/bio_rxiv__2023__07__30__550591-273-6-12?v=ImmunoChemistry+Technologies
Average 92 stars, based on 1 article reviews
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91
ImmunoChemistry Technologies cellmetrix green live dead stain
Cellmetrix Green Live Dead Stain, supplied by ImmunoChemistry Technologies, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
ScienCell alcian blue staining kit
Representative images of multi-lineage differentiation potential of isolated WJ-MSCs and AM-MSCs. WJ-MSCs and AM-MSCs were induced to differentiate toward adipogenic lineage and verified by Alizarin Red <t>S</t> <t>staining</t> (magnification, ×100), osteogenic lineage and verified by Oil Red O staining (magnification, ×200), and chondrogenic lineage and verified by <t>Alcian</t> Blue staining (magnification, ×200). Scale bar, 100 μm. AM-MSCs amniotic membrane mesenchymal stem cells, WJ-MSCs Wharton’s jelly mesenchymal stem cells
Alcian Blue Staining Kit, supplied by ScienCell, 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/live+dead+staining/pmc05359832-81-10-14?v=ScienCell
Average 90 stars, based on 1 article reviews
alcian blue staining kit - by Bioz Stars, 2026-08
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90
Enzo Biochem annexin v-fitc apoptosis detection kit
Representative images of multi-lineage differentiation potential of isolated WJ-MSCs and AM-MSCs. WJ-MSCs and AM-MSCs were induced to differentiate toward adipogenic lineage and verified by Alizarin Red <t>S</t> <t>staining</t> (magnification, ×100), osteogenic lineage and verified by Oil Red O staining (magnification, ×200), and chondrogenic lineage and verified by <t>Alcian</t> Blue staining (magnification, ×200). Scale bar, 100 μm. AM-MSCs amniotic membrane mesenchymal stem cells, WJ-MSCs Wharton’s jelly mesenchymal stem cells
Annexin V Fitc Apoptosis Detection Kit, supplied by Enzo Biochem, 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/live+dead+staining/10__3341_slash_jkos__2018__59__6__549-40-12-25?v=Enzo+Biochem
Average 90 stars, based on 1 article reviews
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90
Becton Dickinson fixable viability stain 780 dye
Representative images of multi-lineage differentiation potential of isolated WJ-MSCs and AM-MSCs. WJ-MSCs and AM-MSCs were induced to differentiate toward adipogenic lineage and verified by Alizarin Red <t>S</t> <t>staining</t> (magnification, ×100), osteogenic lineage and verified by Oil Red O staining (magnification, ×200), and chondrogenic lineage and verified by <t>Alcian</t> Blue staining (magnification, ×200). Scale bar, 100 μm. AM-MSCs amniotic membrane mesenchymal stem cells, WJ-MSCs Wharton’s jelly mesenchymal stem cells
Fixable Viability Stain 780 Dye, 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/live+dead+staining/pmc11227024-389-1-6?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
fixable viability stain 780 dye - by Bioz Stars, 2026-08
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Becton Dickinson live/dead fixable aqua dead cell stain kit
Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of <t>dead</t> cells by Aqua <t>LIVE/DEAD</t> + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.
Live/Dead Fixable Aqua Dead Cell Stain 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/live+dead+staining/pmc09151687-223-9-37?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
live/dead fixable aqua dead cell stain kit - by Bioz Stars, 2026-08
90/100 stars
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90
Beijing Solarbio Science live/dead cell staining kit
Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of <t>dead</t> cells by Aqua <t>LIVE/DEAD</t> + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.
Live/Dead Cell Staining Kit, supplied by Beijing Solarbio Science, 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/live+dead+staining/pm39125251-46-11-18?v=Beijing+Solarbio+Science
Average 90 stars, based on 1 article reviews
live/dead cell staining kit - by Bioz Stars, 2026-08
90/100 stars
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90
Beijing Solarbio Science live/dead cell double staining
Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of <t>dead</t> cells by Aqua <t>LIVE/DEAD</t> + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.
Live/Dead Cell Double Staining, supplied by Beijing Solarbio Science, 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/live+dead+staining/pm36290984-143-0-4?v=Beijing+Solarbio+Science
Average 90 stars, based on 1 article reviews
live/dead cell double staining - by Bioz Stars, 2026-08
90/100 stars
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90
Beijing Solarbio Science live/dead cell staining kit solarbio, beijing, china
Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of <t>dead</t> cells by Aqua <t>LIVE/DEAD</t> + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.
Live/Dead Cell Staining Kit Solarbio, Beijing, China, supplied by Beijing Solarbio Science, 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/live+dead+staining/pm39334225-102-1-5?v=Beijing+Solarbio+Science
Average 90 stars, based on 1 article reviews
live/dead cell staining kit solarbio, beijing, china - by Bioz Stars, 2026-08
90/100 stars
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90
AAT Bioquest iflour 840 maleimide live-dead stain
Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of <t>dead</t> cells by Aqua <t>LIVE/DEAD</t> + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.
Iflour 840 Maleimide Live Dead Stain, supplied by AAT Bioquest, 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/live+dead+staining/pmc11184753-73-18-23?v=AAT+Bioquest
Average 90 stars, based on 1 article reviews
iflour 840 maleimide live-dead stain - by Bioz Stars, 2026-08
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Image Search Results


Representative images of multi-lineage differentiation potential of isolated WJ-MSCs and AM-MSCs. WJ-MSCs and AM-MSCs were induced to differentiate toward adipogenic lineage and verified by Alizarin Red S staining (magnification, ×100), osteogenic lineage and verified by Oil Red O staining (magnification, ×200), and chondrogenic lineage and verified by Alcian Blue staining (magnification, ×200). Scale bar, 100 μm. AM-MSCs amniotic membrane mesenchymal stem cells, WJ-MSCs Wharton’s jelly mesenchymal stem cells

Journal: Stem Cell Research & Therapy

Article Title: Compared to the amniotic membrane, Wharton’s jelly may be a more suitable source of mesenchymal stem cells for cardiovascular tissue engineering and clinical regeneration

doi: 10.1186/s13287-017-0501-x

Figure Lengend Snippet: Representative images of multi-lineage differentiation potential of isolated WJ-MSCs and AM-MSCs. WJ-MSCs and AM-MSCs were induced to differentiate toward adipogenic lineage and verified by Alizarin Red S staining (magnification, ×100), osteogenic lineage and verified by Oil Red O staining (magnification, ×200), and chondrogenic lineage and verified by Alcian Blue staining (magnification, ×200). Scale bar, 100 μm. AM-MSCs amniotic membrane mesenchymal stem cells, WJ-MSCs Wharton’s jelly mesenchymal stem cells

Article Snippet: Sections (4 μm) were deparaffinized in xylene and stained with Alcian Blue Staining Kit (ScienCell, Carlsbad, CA, USA) according to the user’s manual.

Techniques: Isolation, Staining, Membrane

Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of dead cells by Aqua LIVE/DEAD + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.

Journal: The Journal of Clinical Investigation

Article Title: Reprogramming dysfunctional CD8 + T cells to promote properties associated with natural HIV control

doi: 10.1172/JCI157549

Figure Lengend Snippet: Total CD8 + T cells from individuals without HIV were treated with medium, vehicle (Veh.) control, or the GSK3 inhibitor (inh), followed by incubation under basal conditions or with anti-CD3/anti-CD28 stimulation for 48 hours. ( A and B ) Analysis of CD8 + T cell subpopulations in unstimulated cells ( n = 4). ( C ) Fold change of CD8 + T cell subpopulations upon vehicle control or GSK3 inhibitor treatment, relative to the medium alone condition ( n = 4). ( D ) Expression of TCF-1 in CD8 + T cell subsets ( n = 4). ( E ) Fold change in the expression of the indicated markers induced by anti-CD3/anti-CD28 antibody stimulation relative to unstimulated cells ( n = 5). ( F ) Analysis of dead cells by Aqua LIVE/DEAD + staining (Aqua L/D) among total and T-bet + CD8 + T cells, and fold change in dead CD8 + T cells induced by anti-CD3/anti-CD28 stimulation relative to the unstimulated (Unstim.) condition ( n = 5). ( G ) Frequencies of granzyme B + (GZMB + ), IL-2 + , IFN-γ + , and TNF-α + CD8 + T cells after anti-CD3/anti-CD28 stimulation. ( H ) Expression of 1 to 4 functions in CD8 + T cells ( n = 5). * P < 0.05, by Dunn’s test ( B ) and Wilcoxon test ( C , D , and F – H ). Data obtained from 2 ( A – F ) or 3 ( G and H ) independent experiments are shown.

Article Snippet: Purified CD8 + T cells were stained with the LIVE/DEAD Fixable Aqua Dead Cell Stain kit and the following antibodies: anti–CD3 Alexa Fluor 700, anti–CD8 APC Cy7, anti–CCR7 PE Cy7, anti–CD45RA BV421, and anti–CD27 PE (all from BD Biosciences).

Techniques: Incubation, Expressing, Staining