human il 7 Search Results


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Miltenyi Biotec human il 7 miltenyi biotec
Human Il 7 Miltenyi Biotec, supplied by Miltenyi Biotec, 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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Miltenyi Biotec il 7 miltenyi biotec
Il 7 Miltenyi Biotec, supplied by Miltenyi Biotec, 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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Bio X Cell vivo rat igg1 isotype antibody
Vivo Rat Igg1 Isotype Antibody, supplied by Bio X Cell, 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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R&D Systems recombinant human il 7
Recombinant Human Il 7, supplied by R&D 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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Revvity human il 7
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R&D Systems human il 7 duoset elisa development system
Figure 2. MVA-hIL-7-Fc induces the production of functional hIL-7-Fc. (a) Quantification of hIL7-Fc in serum was performed over time after MVA-hIL-7-Fc injection using a specific <t>ELISA.</t> (b) Expression of IL-7 receptor (CD127) at the surface of T cells (percentage of CD3+ cells) and (c) the level of STAT 5 phosphorylation (mean fluorescence intensity (MFI) were evaluated in CD3+ T cells by flow cytometry. Each colored line represents one animal.
Human Il 7 Duoset Elisa Development System, supplied by R&D Systems, 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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R&D Systems recombinant il7
Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, <t>IL7</t> alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.
Recombinant Il7, supplied by R&D Systems, 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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R&D Systems monoclonal mouse anti il 7 primary antibody
Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, <t>IL7</t> alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.
Monoclonal Mouse Anti Il 7 Primary Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems human il 7
Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, <t>IL7</t> alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.
Human Il 7, supplied by R&D Systems, 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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R&D Systems l biotinylated goat anti human il 7 immunoglobulin g antibody
Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, <t>IL7</t> alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.
L Biotinylated Goat Anti Human Il 7 Immunoglobulin G Antibody, supplied by R&D 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 2. MVA-hIL-7-Fc induces the production of functional hIL-7-Fc. (a) Quantification of hIL7-Fc in serum was performed over time after MVA-hIL-7-Fc injection using a specific ELISA. (b) Expression of IL-7 receptor (CD127) at the surface of T cells (percentage of CD3+ cells) and (c) the level of STAT 5 phosphorylation (mean fluorescence intensity (MFI) were evaluated in CD3+ T cells by flow cytometry. Each colored line represents one animal.

Journal: Human vaccines & immunotherapeutics

Article Title: Intravenous injection of a novel viral immunotherapy encoding human interleukin-7 in nonhuman primates is safe and increases absolute lymphocyte count.

doi: 10.1080/21645515.2022.2133914

Figure Lengend Snippet: Figure 2. MVA-hIL-7-Fc induces the production of functional hIL-7-Fc. (a) Quantification of hIL7-Fc in serum was performed over time after MVA-hIL-7-Fc injection using a specific ELISA. (b) Expression of IL-7 receptor (CD127) at the surface of T cells (percentage of CD3+ cells) and (c) the level of STAT 5 phosphorylation (mean fluorescence intensity (MFI) were evaluated in CD3+ T cells by flow cytometry. Each colored line represents one animal.

Article Snippet: The concentration of hIL7-Fc in frozen sera was determined using the human IL-7 DuoSet® ELISA Development System from R&D Systems according to the provider’s instructions.

Techniques: Functional Assay, Injection, Enzyme-linked Immunosorbent Assay, Expressing, Phospho-proteomics, Fluorescence, Flow Cytometry

Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, IL7 alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.

Journal: Gene therapy

Article Title: Generation of multi-functional antigen-specific human T-cells by lentiviral TCR gene transfer.

doi: 10.1038/gt.2010.4

Figure Lengend Snippet: Figure 4 Cytokine-stimulated, TCR-transduced human T-cells maintain CD28 and CD62L expression. CD8+ sorted T-cells were transduced with the lentiviral WT1-TCR after activation with OKT3+IL2, IL2 alone, IL7 alone, IL15 alone, IL15+IL7, IL15+IL21, IL7+IL21 and IL2+IL21 (a). The freshly transduced T-cell populations were then re-stimulated with T2 cells loaded with the specific (pWT126) peptide and irradiated feeder cells in the presence of the same cytokine/s used for transduction. After two rounds of peptide/cytokine stimulation the transduced T- cells were sorted into a Vb2.1-positive population using phycoerythrin-labelled anti-Vb2.1 antibodies and anti-phycoerythrin beads (Miltenyi Biotech, Germany). The purified CD8+ Vb2.1+ T-cells were stimulated for an additional 9 days with pWT126 following which expression of CD28 and CD62L was analysed by FACS. These experiments were representative of three independent experiments. (b) The mean fold increase in the mean fluorescence intensity of CD28 expression following transduction in the presence of IL15 alone or IL15+IL21 as compared with OKT3+IL2 is shown. Statistical significance was determined as Po0.05 using a two-tailed t-test. FACS, fluorescence-activated cell sorting; IL, interleukin; TCR, T-cell receptor.

Article Snippet: The concentration of common g-chain cytokines used either alone or in combination as stated was as follows: 20 U ml 1 of human recombinant IL2 (Roche, Basel, Switzerland), 5 ng ml 1 human recombinant IL7 (R&D Systems, Abingdon, Oxfordshire, UK), 10 ng ml 1 human recombinant IL15 (R&D Systems) and 30 ng ml 1 mouse recombinant IL21 (R&D Systems).

Techniques: Expressing, Transduction, Activation Assay, Irradiation, Two Tailed Test, FACS