fixable viability staining-efluor780 Search Results


efluor780 conjugated fvd  (Thermo Fisher)
99
Thermo Fisher efluor780 conjugated fvd
Efluor780 Conjugated Fvd, 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/fixable+viability+staining-efluor780/Fluorescein/pmc05442621-303-4-6
Average 99 stars, based on 1 article reviews
efluor780 conjugated fvd - by Bioz Stars, 2026-09
99/100 stars
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fixable viability stain efluor780  (Becton Dickinson)
90
Becton Dickinson fixable viability stain efluor780
Labile zinc levels increase in primary epithelial cells. (A) SAECs were infected with RSV at an MOI of 3, and cells were stained with ZP-1 at 24 h p.i. and 48 h p.i. (B) Cell viability was determined by staining the cells with the fixable viability dye <t>eFluor780.</t> (C) Nasal epithelial cells isolated from nasopharyngeal aspirates were stained with ZP-1. Labile zinc levels are presented as median fluorescence intensities (MFI). (D) The cell viability of NPA specimens was determined by staining the cells with the fixable viability dye eFluor780. There were 10 controls and 7 cases. (E) A549 cells were infected with RSV and DENV at MOIs of 0.3 and 5, respectively. Cells were stained with Annexin-V and eFluor780 dye at 24 h p.i. and 48 h p.i. Cell populations represent different phases: healthy, early apoptosis, late apoptosis, and necrosis. Annexin-V signal was detected in FITC filter and eFluor-780 signal was detected in APC-Cy-7 filter. Data are from at least two independent experiments. *, P < 0.05; **, P < 0.01; ns, differences were not significant.
Fixable Viability Stain Efluor780, 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/fixable+viability+staining-efluor780/allophycocyanin+conjugated+antibodies/pmc07253603-222-21-25
Average 90 stars, based on 1 article reviews
fixable viability stain efluor780 - by Bioz Stars, 2026-09
90/100 stars
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fixable viability dye efluor780  (Thermo Fisher)
99
Thermo Fisher fixable viability dye efluor780
Labile zinc levels increase in primary epithelial cells. (A) SAECs were infected with RSV at an MOI of 3, and cells were stained with ZP-1 at 24 h p.i. and 48 h p.i. (B) Cell viability was determined by staining the cells with the fixable viability dye <t>eFluor780.</t> (C) Nasal epithelial cells isolated from nasopharyngeal aspirates were stained with ZP-1. Labile zinc levels are presented as median fluorescence intensities (MFI). (D) The cell viability of NPA specimens was determined by staining the cells with the fixable viability dye eFluor780. There were 10 controls and 7 cases. (E) A549 cells were infected with RSV and DENV at MOIs of 0.3 and 5, respectively. Cells were stained with Annexin-V and eFluor780 dye at 24 h p.i. and 48 h p.i. Cell populations represent different phases: healthy, early apoptosis, late apoptosis, and necrosis. Annexin-V signal was detected in FITC filter and eFluor-780 signal was detected in APC-Cy-7 filter. Data are from at least two independent experiments. *, P < 0.05; **, P < 0.01; ns, differences were not significant.
Fixable Viability Dye Efluor780, 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/fixable+viability+staining-efluor780/PBS/pmc12127132-66-19-23
Average 99 stars, based on 1 article reviews
fixable viability dye efluor780 - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier

Image Search Results


Labile zinc levels increase in primary epithelial cells. (A) SAECs were infected with RSV at an MOI of 3, and cells were stained with ZP-1 at 24 h p.i. and 48 h p.i. (B) Cell viability was determined by staining the cells with the fixable viability dye eFluor780. (C) Nasal epithelial cells isolated from nasopharyngeal aspirates were stained with ZP-1. Labile zinc levels are presented as median fluorescence intensities (MFI). (D) The cell viability of NPA specimens was determined by staining the cells with the fixable viability dye eFluor780. There were 10 controls and 7 cases. (E) A549 cells were infected with RSV and DENV at MOIs of 0.3 and 5, respectively. Cells were stained with Annexin-V and eFluor780 dye at 24 h p.i. and 48 h p.i. Cell populations represent different phases: healthy, early apoptosis, late apoptosis, and necrosis. Annexin-V signal was detected in FITC filter and eFluor-780 signal was detected in APC-Cy-7 filter. Data are from at least two independent experiments. *, P < 0.05; **, P < 0.01; ns, differences were not significant.

Journal: mSphere

Article Title: Respiratory Syncytial Virus-Induced Oxidative Stress Leads to an Increase in Labile Zinc Pools in Lung Epithelial Cells

doi: 10.1128/mSphere.00447-20

Figure Lengend Snippet: Labile zinc levels increase in primary epithelial cells. (A) SAECs were infected with RSV at an MOI of 3, and cells were stained with ZP-1 at 24 h p.i. and 48 h p.i. (B) Cell viability was determined by staining the cells with the fixable viability dye eFluor780. (C) Nasal epithelial cells isolated from nasopharyngeal aspirates were stained with ZP-1. Labile zinc levels are presented as median fluorescence intensities (MFI). (D) The cell viability of NPA specimens was determined by staining the cells with the fixable viability dye eFluor780. There were 10 controls and 7 cases. (E) A549 cells were infected with RSV and DENV at MOIs of 0.3 and 5, respectively. Cells were stained with Annexin-V and eFluor780 dye at 24 h p.i. and 48 h p.i. Cell populations represent different phases: healthy, early apoptosis, late apoptosis, and necrosis. Annexin-V signal was detected in FITC filter and eFluor-780 signal was detected in APC-Cy-7 filter. Data are from at least two independent experiments. *, P < 0.05; **, P < 0.01; ns, differences were not significant.

Article Snippet: Cells were incubated for 30 min at 37°C in a CO 2 incubator and mixed every 10 min. After 30 min, fixable viability stain eFluor780 (Becton, Dickinson Biosciences) was added to the cells at a 1:500 dilution, prepared in the staining medium, and incubated for a further 10 min at 37°C in the CO 2 incubator.

Techniques: Infection, Staining, Isolation, Fluorescence