Cytokine Kits Search Results


97
Miltenyi Biotec macsplex 12 cytokine 389 kit
Macsplex 12 Cytokine 389 Kit, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
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KCAS Bioanalytical and Biomarker Services kcas bio analytical
Kcas Bio Analytical, supplied by KCAS Bioanalytical and Biomarker Services, 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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Average 99 stars, based on 1 article reviews
kcas bio analytical - by Bioz Stars, 2026-04
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90
Diaclone enzyme linked immunosorbent assay kits specific for the rat cytokines
Enzyme Linked Immunosorbent Assay Kits Specific For The Rat Cytokines, supplied by Diaclone, 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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Panomics Inc multiplex kits
Multiplex Kits, supplied by Panomics Inc, 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
multiplex kits - by Bioz Stars, 2026-04
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4A Biotech cytokine elisa kits
Cytokine Elisa Kits, supplied by 4A Biotech, 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
cytokine elisa kits - by Bioz Stars, 2026-04
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Becton Dickinson human elisa kits cytokines ifn-γ, il-2, tnf-α
Kinetics of cytokine secretion by activated naive and memory CD4+ T cells. Naive and memory CD4+ T cells were isolated from CD4+ T cells by MACS microbeads, and the purity of naive or memory CD4+ T cells was more than 97% as determined by flow cytometry (a). Naive and memory CD4+ T cells were stimulated with (open histogram) or without (shaded histogram) PMA and ionomycin in the presence of BFA for 6 h. Cells were stained by intracellular staining and analyzed by FACS (b). Purified naive and memory CD4+ T cells were stimulated with immobilized anti-CD3 (1 μg/ml) and anti-CD28 (1 μg/ml) for 0 to 72 h, and the concentrations of cytokines IFN-γ, IL-2, <t>and</t> <t>TNF-α</t> were detected by ELISA (c). Data are representative of three separate experiments with similar results.
Human Elisa Kits Cytokines Ifn γ, Il 2, Tnf α, 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/result/human elisa kits cytokines ifn-γ, il-2, tnf-α/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
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Becton Dickinson cytokine bead array cba detection kit
NanoATV regulation of <t>cytokine</t> profiles in HIV-1 infected MDM. MDM were treated with 100 μM native ATV or nanoATV and infected with HIV-1 at day 0, 5 or 10 post-drug treatment. Untreated, uninfected cells were used as controls. After 24 hours of viral infection, cell culture media were collected and analyzed using a cytokine bead array. (A) Density plots show expression of IL-12, TNF, IL-10, IL-6, IL-1β and IL-8 for control, treated, HIV-1 infected and treated infected MDM. Cytokine levels were detected by FACSArray cytometer and data was plotted using FlowJo (version 10.7) software. (B) Levels of IL-12 and TNF after treatment and infection are shown. Data are analyzed using FCAP software and values of cytokine expression were expressed as pg/mL.
Cytokine Bead Array Cba Detection 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/result/cytokine bead array cba detection kit/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
cytokine bead array cba detection kit - by Bioz Stars, 2026-04
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Becton Dickinson ifn- γ il-5 cytokine elisa kits
Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of <t>IFN-</t> γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.
Ifn γ Il 5 Cytokine Elisa Kits, 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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Average 90 stars, based on 1 article reviews
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90
LINCO high sensitivity human cytokine kit
Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of <t>IFN-</t> γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.
High Sensitivity Human Cytokine Kit, supplied by LINCO, 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
high sensitivity human cytokine kit - by Bioz Stars, 2026-04
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Life Sciences Advanced Technologies ang-1 and ang-2 cytokine assay kits
Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of <t>IFN-</t> γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.
Ang 1 And Ang 2 Cytokine Assay Kits, supplied by Life Sciences Advanced Technologies, 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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Becton Dickinson fastimmune intracellular cytokine detection kits
Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of <t>IFN-</t> γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.
Fastimmune Intracellular Cytokine Detection Kits, 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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Average 90 stars, based on 1 article reviews
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GENORISE SCIENTIFIC INC chicken cytokine elisa kits
Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of <t>IFN-</t> γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.
Chicken Cytokine Elisa Kits, supplied by GENORISE SCIENTIFIC INC, 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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Image Search Results


Kinetics of cytokine secretion by activated naive and memory CD4+ T cells. Naive and memory CD4+ T cells were isolated from CD4+ T cells by MACS microbeads, and the purity of naive or memory CD4+ T cells was more than 97% as determined by flow cytometry (a). Naive and memory CD4+ T cells were stimulated with (open histogram) or without (shaded histogram) PMA and ionomycin in the presence of BFA for 6 h. Cells were stained by intracellular staining and analyzed by FACS (b). Purified naive and memory CD4+ T cells were stimulated with immobilized anti-CD3 (1 μg/ml) and anti-CD28 (1 μg/ml) for 0 to 72 h, and the concentrations of cytokines IFN-γ, IL-2, and TNF-α were detected by ELISA (c). Data are representative of three separate experiments with similar results.

Journal: The Journal of Biological Chemistry

Article Title: Human Memory, but Not Naive, CD4 + T Cells Expressing Transcription Factor T-bet Might Drive Rapid Cytokine Production *

doi: 10.1074/jbc.M114.608745

Figure Lengend Snippet: Kinetics of cytokine secretion by activated naive and memory CD4+ T cells. Naive and memory CD4+ T cells were isolated from CD4+ T cells by MACS microbeads, and the purity of naive or memory CD4+ T cells was more than 97% as determined by flow cytometry (a). Naive and memory CD4+ T cells were stimulated with (open histogram) or without (shaded histogram) PMA and ionomycin in the presence of BFA for 6 h. Cells were stained by intracellular staining and analyzed by FACS (b). Purified naive and memory CD4+ T cells were stimulated with immobilized anti-CD3 (1 μg/ml) and anti-CD28 (1 μg/ml) for 0 to 72 h, and the concentrations of cytokines IFN-γ, IL-2, and TNF-α were detected by ELISA (c). Data are representative of three separate experiments with similar results.

Article Snippet: Human ELISA kits for cytokines IFN-γ, IL-2, and TNF-α were purchased from BD Biosciences.

Techniques: Isolation, Flow Cytometry, Staining, Purification, Enzyme-linked Immunosorbent Assay

NanoATV regulation of cytokine profiles in HIV-1 infected MDM. MDM were treated with 100 μM native ATV or nanoATV and infected with HIV-1 at day 0, 5 or 10 post-drug treatment. Untreated, uninfected cells were used as controls. After 24 hours of viral infection, cell culture media were collected and analyzed using a cytokine bead array. (A) Density plots show expression of IL-12, TNF, IL-10, IL-6, IL-1β and IL-8 for control, treated, HIV-1 infected and treated infected MDM. Cytokine levels were detected by FACSArray cytometer and data was plotted using FlowJo (version 10.7) software. (B) Levels of IL-12 and TNF after treatment and infection are shown. Data are analyzed using FCAP software and values of cytokine expression were expressed as pg/mL.

Journal: Retrovirology

Article Title: Opposing regulation of endolysosomal pathways by long-acting nanoformulated antiretroviral therapy and HIV-1 in human macrophages

doi: 10.1186/s12977-014-0133-5

Figure Lengend Snippet: NanoATV regulation of cytokine profiles in HIV-1 infected MDM. MDM were treated with 100 μM native ATV or nanoATV and infected with HIV-1 at day 0, 5 or 10 post-drug treatment. Untreated, uninfected cells were used as controls. After 24 hours of viral infection, cell culture media were collected and analyzed using a cytokine bead array. (A) Density plots show expression of IL-12, TNF, IL-10, IL-6, IL-1β and IL-8 for control, treated, HIV-1 infected and treated infected MDM. Cytokine levels were detected by FACSArray cytometer and data was plotted using FlowJo (version 10.7) software. (B) Levels of IL-12 and TNF after treatment and infection are shown. Data are analyzed using FCAP software and values of cytokine expression were expressed as pg/mL.

Article Snippet: 24 hours after drug treatment, 50 μL cell culture media from treated and infected MDM were tested to determine the concentrations of inflammatory cytokines measured by a cytokine bead array (CBA) detection kit (Becton Dickinson Biosciences; Mississauga, ON, USA) and performed according to instructions of the manufacturer.

Techniques: Infection, Cell Culture, Expressing, Control, Cytometry, Software

Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of IFN- γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.

Journal: BioMed Research International

Article Title: A De- O -acylated Lipooligosaccharide-Based Adjuvant System Promotes Antibody and Th1-Type Immune Responses to H1N1 Pandemic Influenza Vaccine in Mice

doi: 10.1155/2016/3713656

Figure Lengend Snippet: Th1-type-predominant immune response to CIA06-adjuvanted influenza vaccine. Splenocytes were isolated from the mice that had been immunized as described in and cultured for 72 h in the absence (■) or presence of Greenflu-S (■). The levels of IFN- γ (a) and IL-5 (b) in the culture media were determined by sandwich ELISA, and IFN- γ : IL-5 ratios were calculated for each group (c). Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.

Article Snippet: Recombinant mouse IL-2 was acquired from R&D Systems (Minneapolis, MN, USA), and IFN- γ and IL-5 cytokine ELISA kits were obtained from BD Biosciences (San Diego, CA, USA) and R&D Systems.

Techniques: Isolation, Cell Culture, Sandwich ELISA, Comparison

CIA06-adjuvanted influenza vaccine stimulates both CD4 + and CD8 + T cell responses. Splenocytes were isolated from the mice ( n = 6) that had been immunized twice at a 3-week interval with nonadjuvanted or adjuvanted Greenflu-S (0.2 μ g) and stimulated with the vaccine for 72 h in the absence or presence of anti-CD4 and/or anti-CD8 antibodies. IFN- γ levels in the culture media were determined by sandwich ELISA. Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.

Journal: BioMed Research International

Article Title: A De- O -acylated Lipooligosaccharide-Based Adjuvant System Promotes Antibody and Th1-Type Immune Responses to H1N1 Pandemic Influenza Vaccine in Mice

doi: 10.1155/2016/3713656

Figure Lengend Snippet: CIA06-adjuvanted influenza vaccine stimulates both CD4 + and CD8 + T cell responses. Splenocytes were isolated from the mice ( n = 6) that had been immunized twice at a 3-week interval with nonadjuvanted or adjuvanted Greenflu-S (0.2 μ g) and stimulated with the vaccine for 72 h in the absence or presence of anti-CD4 and/or anti-CD8 antibodies. IFN- γ levels in the culture media were determined by sandwich ELISA. Statistical differences were analyzed by one-way ANOVA followed by Tukey's multiple comparison test. Results are expressed as the means ± SD of values obtained from triplicate cultures that used two spleens each. Data shown are representative of three independent experiments. ∗ P < 0.05; ∗∗ P < 0.01; and ∗∗∗ P < 0.001. NS, not significant.

Article Snippet: Recombinant mouse IL-2 was acquired from R&D Systems (Minneapolis, MN, USA), and IFN- γ and IL-5 cytokine ELISA kits were obtained from BD Biosciences (San Diego, CA, USA) and R&D Systems.

Techniques: Isolation, Sandwich ELISA, Comparison