duoset elisa development system Search Results


human m-csf duoset elisa  (Bio-Techne corporation)
92
Bio-Techne corporation human m-csf duoset elisa
Human M Csf Duoset Elisa, supplied by Bio-Techne corporation, 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/result/human m-csf duoset elisa/product/Bio-Techne corporation
Average 92 stars, based on 1 article reviews
human m-csf duoset elisa - by Bioz Stars, 2026-03
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human interleukin-6 (il-6) assaymax elisa kit  (Assaypro)
96
Assaypro human interleukin-6 (il-6) assaymax elisa kit
Human Interleukin 6 (Il 6) Assaymax Elisa Kit, supplied by Assaypro, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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elisa development kit for mouse il-12p40  (Genzyme)
90
Genzyme elisa development kit for mouse il-12p40
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Elisa Development Kit For Mouse Il 12p40, supplied by Genzyme, 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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duoset cytokinespecific elisa kits  (Genzyme)
90
Genzyme duoset cytokinespecific elisa kits
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Duoset Cytokinespecific Elisa Kits, supplied by Genzyme, 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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duoset enzyme-linked immunosorbent assays  (USCN Life)
90
USCN Life duoset enzyme-linked immunosorbent assays
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Duoset Enzyme Linked Immunosorbent Assays, supplied by USCN Life, 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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elisa kits duoset®elisa development system  (USCN Life)
90
USCN Life elisa kits duoset®elisa development system
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Elisa Kits Duoset®Elisa Development System, supplied by USCN Life, 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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human tgf-b duoset elisa development system  (Genzyme)
90
Genzyme human tgf-b duoset elisa development system
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Human Tgf B Duoset Elisa Development System, supplied by Genzyme, 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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duoset elisa development kits  (Panomics Inc)
90
Panomics Inc duoset elisa development kits
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Duoset Elisa Development 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
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il-2 or ifn-g duoset elisa development system  (Genzyme)
90
Genzyme il-2 or ifn-g duoset elisa development system
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Il 2 Or Ifn G Duoset Elisa Development System, supplied by Genzyme, 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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ifn-g, il-2, or il-4 duoset elisa development system  (Genzyme)
90
Genzyme ifn-g, il-2, or il-4 duoset elisa development system
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Ifn G, Il 2, Or Il 4 Duoset Elisa Development System, supplied by Genzyme, 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/ifn-g, il-2, or il-4 duoset elisa development system/product/Genzyme
Average 90 stars, based on 1 article reviews
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human ccl11/eotaxin duoset elisa  (Bio-Techne corporation)
91
Bio-Techne corporation human ccl11/eotaxin duoset elisa
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Human Ccl11/Eotaxin Duoset Elisa, supplied by Bio-Techne corporation, 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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duoset enzyme-linked immunosorbent assay development system [tecan: desacylghrelin (human) easy sampling elisa]  (Tecan Systems)
90
Tecan Systems duoset enzyme-linked immunosorbent assay development system [tecan: desacylghrelin (human) easy sampling elisa]
Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon <t>(IFN)‐γ</t> (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme <t>linked</t> <t>immunosorbent</t> assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.
Duoset Enzyme Linked Immunosorbent Assay Development System [Tecan: Desacylghrelin (Human) Easy Sampling Elisa], supplied by Tecan Systems, 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


Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon (IFN)‐γ (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme linked immunosorbent assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.

Journal:

Article Title: Role of interleukin 15 in colitis induced by dextran sulphate sodium in mice

doi: 10.1136/gut.2005.076000

Figure Lengend Snippet: Figure 5 Effects of in vivo treatment with anti‐CD8 monoclonal antibody (mAb) and asialo‐GM1 Abs on dextran sulphate sodium (DSS) induced colitis in C57BL/6 mice. (A) For in vivo cell depletion, both anti‐CD8 mAb and anti‐asialo GM1 Ab or isotype control IgG was injected intraperitoneally into C57BL/6 mice once a week from two days before administration of DSS. Survival rates of these mice administered 2% DSS were monitored every day (n = 5 per group). (B–D) Lamina propria (LP) cells from anti‐CD8 and asialo‐GM1 treated mice or control IgG treated mice on day 5 after DSS administration or naïve C57BL/6 mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Tumour necrosis factor (TNF)‐α (B), interferon (IFN)‐γ (C), and IL‐12p40 (D) concentrations in culture supernatants of LP cells were determined by enzyme linked immunosorbent assay (n = 4 per group). Statistically significant differences are shown. ND, not detectable.

Article Snippet: Cytokine activity was assayed by enzyme linked immunosorbent assay (ELISA) using an ELISA Development Kit for mouse IFN‐γ, tumour necrosis factor (TNF)‐α, IL‐1β, IL‐6, IL‐10, and IL‐12p40 (Genzyme Diagnostics, Cambridge, Massachusetts, USA).

Techniques: In Vivo, Control, Injection, Cell Culture, Enzyme-linked Immunosorbent Assay

Figure 6 Dextran sulphate sodium (DSS) induced chronic colitis in interleukin (IL)‐15 knockout (KO) mice. IL‐15 KO mice and wild‐type (WT) mice were administered 2% DSS on days 0–5, 10–15, and 20–25. Body weight (A) and disease activity index (B) were monitored every day and values for body weight are expressed as percentage of body weight on day 0. Each point represents the mean (SD) (n = 7 per group). (C–E) Lamina propria (LP) cells from IL‐15 KO mice or WT mice on day 30 after DSS administration or naïve IL‐15 KO mice or WT mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Production of tumour necrosis factor (TNF)‐α (C), interferon (IFN)‐γ (D), or IL‐12p40 (E) in culture supernatants of LP cells was determined by enzyme linked immunosorbent assay (n = 4 per group). Statistically significant differences are shown: * p<0.05. ND, not detectable.

Journal:

Article Title: Role of interleukin 15 in colitis induced by dextran sulphate sodium in mice

doi: 10.1136/gut.2005.076000

Figure Lengend Snippet: Figure 6 Dextran sulphate sodium (DSS) induced chronic colitis in interleukin (IL)‐15 knockout (KO) mice. IL‐15 KO mice and wild‐type (WT) mice were administered 2% DSS on days 0–5, 10–15, and 20–25. Body weight (A) and disease activity index (B) were monitored every day and values for body weight are expressed as percentage of body weight on day 0. Each point represents the mean (SD) (n = 7 per group). (C–E) Lamina propria (LP) cells from IL‐15 KO mice or WT mice on day 30 after DSS administration or naïve IL‐15 KO mice or WT mice (DSS(−)) were prepared and cultured without stimulation for 24 hours at 37°C. Production of tumour necrosis factor (TNF)‐α (C), interferon (IFN)‐γ (D), or IL‐12p40 (E) in culture supernatants of LP cells was determined by enzyme linked immunosorbent assay (n = 4 per group). Statistically significant differences are shown: * p<0.05. ND, not detectable.

Article Snippet: Cytokine activity was assayed by enzyme linked immunosorbent assay (ELISA) using an ELISA Development Kit for mouse IFN‐γ, tumour necrosis factor (TNF)‐α, IL‐1β, IL‐6, IL‐10, and IL‐12p40 (Genzyme Diagnostics, Cambridge, Massachusetts, USA).

Techniques: Knock-Out, Activity Assay, Cell Culture, Enzyme-linked Immunosorbent Assay