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Miltenyi Biotec apc anti human il
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
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Proteintech il 10
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
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Miltenyi Biotec anti il 10 apc
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
Anti Il 10 Apc, supplied by Miltenyi Biotec, 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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Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
Anti Human Il 10 Pe Cyanine 7 Clone Jes3 97d, supplied by Thermo Fisher, 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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Thermo Fisher anti-human il-10
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
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Cusabio anti inflammatory cytokine il 10
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
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Thermo Fisher anti‑human il‑10‑pe‑cyanine 7 (jes3‑9d7)
Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies <t>of</t> <t>IL-10</t> producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001
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Miltenyi Biotec allophycocyanin apc conjugated anti human syndecan
QGP-1 and COA109 cells express HSV entry receptors. ( A ) The cell surface expression of viral entry receptors for M002 (CD111, CD112, <t>syndecan,</t> and HVEM) was assessed utilizing flow cytometry. QGP-1 (10 6 ) or COA109 (10 6 ) cells were cultured overnight in 6-well plates, collected, stained with fluorescent <t>conjugated</t> antibody, and evaluated with flow cytometry. Cells treated with FcR blocker alone served as negative controls. Receptors were expressed in variable quantities, but all four receptors were present on both cell types. ( B ) Representative histograms of flow cytometry for viral entry receptors in QGP-1 cells. Data represent three biologic replicates and are reported as mean ± standard error of the mean (SEM). * p ≤ 0.05, ** p ≤ 0.01, COA109 vs QGP-1.
Allophycocyanin Apc Conjugated Anti Human Syndecan, supplied by Miltenyi Biotec, 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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Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies of IL-10 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001

Journal: Gut Pathogens

Article Title: “ Bifidobacterium longum -reactive T helper cells as marker for intestinal barrier impairment in ICU patients with sepsis”

doi: 10.1186/s13099-025-00770-9

Figure Lengend Snippet: Cytokine production in antigen-reactive CD4 + CD154 + Th cells in cohort 2. ( A ) Frequencies of IL-17 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( B ) Frequencies of IL-4 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans , or B. longum ( n = 10/10/10). ( C ) Frequencies of IL-10 producing CD4 + CD154 + Th cells after stimulation with E. coli , C. albicans or B. longum ( n = 10/10/10). Data represented as mean ± SEM. * p < 0.05, ** p < 0.01, and *** p < 0.001

Article Snippet: The enriched cell fractions were fixed with eBioscienceTM, FoxP3 staining buffer (Thermo Fisher Scientific, Waltham, MA USA), and subsequently intracellularly stained ( Panel 1 : APC anti-human IFNγ; APC/Cy7 anti-human IL-2; PerCP/Cy5.5 anti-human TNFα; all from BioLegend, Koblenz, Germany; FITC anti-human CD154 from Miltenyi Biotec, Bergisch Gladbach, Germany; Panel 2 : PerCP/Cy5.5 anti-human IL-4; APC anti-human IL-10; APC/Cy7 anti-human IL-17a all from BioLegend; FITC anti-human CD154 from Miltenyi Biotec, Bergisch Gladbach, Germany).

Techniques:

QGP-1 and COA109 cells express HSV entry receptors. ( A ) The cell surface expression of viral entry receptors for M002 (CD111, CD112, syndecan, and HVEM) was assessed utilizing flow cytometry. QGP-1 (10 6 ) or COA109 (10 6 ) cells were cultured overnight in 6-well plates, collected, stained with fluorescent conjugated antibody, and evaluated with flow cytometry. Cells treated with FcR blocker alone served as negative controls. Receptors were expressed in variable quantities, but all four receptors were present on both cell types. ( B ) Representative histograms of flow cytometry for viral entry receptors in QGP-1 cells. Data represent three biologic replicates and are reported as mean ± standard error of the mean (SEM). * p ≤ 0.05, ** p ≤ 0.01, COA109 vs QGP-1.

Journal: Scientific Reports

Article Title: Investigation of an oncolytic herpes simplex virus as a potential therapeutic agent for gastroenteropancreatic neuroendocrine neoplasms

doi: 10.1038/s41598-025-98588-7

Figure Lengend Snippet: QGP-1 and COA109 cells express HSV entry receptors. ( A ) The cell surface expression of viral entry receptors for M002 (CD111, CD112, syndecan, and HVEM) was assessed utilizing flow cytometry. QGP-1 (10 6 ) or COA109 (10 6 ) cells were cultured overnight in 6-well plates, collected, stained with fluorescent conjugated antibody, and evaluated with flow cytometry. Cells treated with FcR blocker alone served as negative controls. Receptors were expressed in variable quantities, but all four receptors were present on both cell types. ( B ) Representative histograms of flow cytometry for viral entry receptors in QGP-1 cells. Data represent three biologic replicates and are reported as mean ± standard error of the mean (SEM). * p ≤ 0.05, ** p ≤ 0.01, COA109 vs QGP-1.

Article Snippet: Briefly, phycoerythrin (PE) conjugated anti-human CD111 antibody (10 μL, Miltenyi Biotec), PE anti-human CD112 antibody (10 μL, Miltenyi Biotec), allophycocyanin (APC) conjugated anti-human syndecan (10 μL, Miltenyi Biotec), or APC anti-human HVEM (10 μL, Miltenyi Biotec), were added for 20 min on ice in the dark.

Techniques: Expressing, Flow Cytometry, Cell Culture, Staining