fixable viability stain dye efluor780 Search Results


fixable viability dye efluor 780  (Thermo Fisher)
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Thermo Fisher fixable viability dye efluor 780
Fixable Viability Dye Efluor 780, 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
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anti-cd8 apc-efluor 780  (Becton Dickinson)
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Becton Dickinson anti-cd8 apc-efluor 780
Anti Cd8 Apc Efluor 780, 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
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streptavidin apc efluor780  (Thermo Fisher)
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Thermo Fisher streptavidin apc efluor780
Streptavidin Apc 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
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recombinant proteins l d apc efluor780 dye ebioscience 65 0865 14 dap  (Thermo Fisher)
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Thermo Fisher recombinant proteins l d apc efluor780 dye ebioscience 65 0865 14 dap
Recombinant Proteins L D Apc Efluor780 Dye Ebioscience 65 0865 14 Dap, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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trypan blue fixable viability dye efluor 780  (Thermo Fisher)
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Thermo Fisher trypan blue fixable viability dye efluor 780
Trypan Blue Fixable Viability Dye Efluor 780, 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
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fixable viability dye efluor 780  (Becton Dickinson)
90
Becton Dickinson fixable viability dye efluor 780
Fixable Viability Dye Efluor 780, 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
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cd45 2 apc efluor 780 ebioscience  (Thermo Fisher)
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Thermo Fisher cd45 2 apc efluor 780 ebioscience
Cd45 2 Apc Efluor 780 Ebioscience, 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
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apce780 anti-mouse tcrβ  (Becton Dickinson)
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Becton Dickinson apce780 anti-mouse tcrβ

Apce780 Anti Mouse Tcrβ, 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
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pe rat anti-mouse cd14  (Becton Dickinson)
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Becton Dickinson pe rat anti-mouse cd14
In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + <t>CD11c</t> + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.
Pe Rat Anti Mouse Cd14, 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
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anti-cd3  (Becton Dickinson)
90
Becton Dickinson anti-cd3
In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + <t>CD11c</t> + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.
Anti Cd3, 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
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fixable viability dye efluor 780  (Avantor)
90
Avantor fixable viability dye efluor 780
In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + <t>CD11c</t> + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.
Fixable Viability Dye Efluor 780, supplied by Avantor, 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
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apc efluor 780 anti cd127 a7r34 ebioscience  (Thermo Fisher)
99
Thermo Fisher apc efluor 780 anti cd127 a7r34 ebioscience
In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + <t>CD11c</t> + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.
Apc Efluor 780 Anti Cd127 A7r34 Ebioscience, 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
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Image Search Results


Journal: Cell reports

Article Title: Intestinal IL-17R Signaling Constrains IL-18-Driven Liver Inflammation by the Regulation of Microbiome-Derived Products

doi: 10.1016/j.celrep.2019.10.042

Figure Lengend Snippet:

Article Snippet: Flow cytometry antibodies used included: Live/Dead fixable aqua dead cell stain (Invivogen) (1:500 dilution), BV786 Anti-mouse CD4 (BD Clone RM4–5) (1:200 dilution, APC Anti-mouse IFNγ (eBiosciences Clone XMG1.2) (1:200 dilution), APCe780 Anti-mouse TCRβ (BD Clone H57–597) dilution), BV421 Anti-mouse NK1.1 (BD clone PK136) (1:100 dilution), BUV395 Anti-mouse CD3 (BD Clone 145–2C11) (1:200 dilution), PCP-Cy5 Rat-Anti-Mouse CD3 Molecular Complex (BD clone 17A2) (1:200 dilution), BV605 Anti-Mouse CD90.2 (BD clone 30-H12) (1:400 dilution), PE Anti-Mouse FasL (Biolegend Clone MFL3) (1:200 dilution), PE-Cy7 Anti-mouse CD8 (Invitrogen clone eBioH35–7.2) (1:400 dilution), Anti-Mouse CD16/CD32 (eBioscience Clone 93).

Techniques: Recombinant, Purification, Activity Assay, In Situ, Enzyme-linked Immunosorbent Assay, Bicinchoninic Acid Protein Assay, Staining, RNA Sequencing Assay, Sequencing, Software, SYBR Green Assay, Protease Inhibitor, Cell Counting

In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + CD11c + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.

Journal: Viruses

Article Title: Identification of Broad-Spectrum Antiviral Compounds by Targeting Viral Entry

doi: 10.3390/v11020176

Figure Lengend Snippet: In vivo activity of Tyrphostin A9, Monensin, and Sofosbuvir. ( A ) Schematic of the drug treatment and infection regime in AG129 mice. Mice were treated with 5.7 mg/kg of Sofosbuvir, 10 mg/kg of Monensin, or 1mg/kg of Tyrphostin A9 before and after infection with 10 5 pfu of ZIKV, at the indicated intervals. Administration of Tyrphostin A9 was suspended at day 3 due to toxicity. Focus-forming units (ffu, top panels) and ZIKV RNA copies (bottom panels) per ml of serum at day 1, 3, and 7 p.i. upon treatment with Sofosbuvir ( B ), Monensin ( C ), or Tyrphostin A9 ( D ). N.D. (not detected), indicates that no infectious units were recovered. ZIKV RNA copies/ng at day 7 p.i. in the lymph nodes ( E ), liver ( F ), and brain ( G ) upon indicated treatment. Percentages of CD14 + CD11b + macrophages ( H ), CD14 + CD11c + DC ( I ), and CD3 + CD4 + T cells ( J ) infected with ZIKV at day 7 p.i. upon indicated treatment. P values from unpaired T tests are displayed for statistically significant comparisons.

Article Snippet: PE-Cy7 rat anti-mouse CD11b, APC-eFluor780 rat anti-mouse CD11c, PE rat anti-mouse CD14, Pacific blue rat anti-mouse CD3, eFluor650 rat anti-mouse CD4 and APC rat anti-mouse CD8a were from BD Biosciences (UK).

Techniques: In Vivo, Activity Assay, Infection