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il5  (Shanghai Korain Biotech Co Ltd)
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Shanghai Korain Biotech Co Ltd il5
Il5, supplied by Shanghai Korain Biotech Co Ltd, 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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gene exp il5 mm00439646 m1  (Thermo Fisher)
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Thermo Fisher gene exp il5 mm00439646 m1
( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of <t>Il5</t> mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .
Gene Exp Il5 Mm00439646 M1, 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 il5 pe  (Miltenyi Biotec)
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( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of <t>Il5</t> mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .
Anti Il5 Pe, 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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il 5  (Sino Biological)
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Sino Biological il 5
( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of <t>Il5</t> mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .
Il 5, supplied by Sino Biological, 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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il 5  (Boster Bio)
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Boster Bio il 5
( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of <t>Il5</t> mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .
Il 5, supplied by Boster Bio, 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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gene exp il5 hs01548712 g1  (Thermo Fisher)
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Thermo Fisher gene exp il5 hs01548712 g1
( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of <t>Il5</t> mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .
Gene Exp Il5 Hs01548712 G1, 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
https://www.bioz.com/result/gene exp il5 hs01548712 g1/product/Thermo Fisher
Average 95 stars, based on 1 article reviews
gene exp il5 hs01548712 g1 - by Bioz Stars, 2026-05
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Image Search Results


( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of Il5 mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .

Journal: EMBO Molecular Medicine

Article Title: Metabolically reprogrammed eosinophils impair T cell immunity and cause chronic skin infection

doi: 10.1038/s44321-026-00392-x

Figure Lengend Snippet: ( A ) Left, representative flow cytometric analysis of foot skin cells, isolated from C57BL/6 mice and gated for CD11b + SiglecF + eosinophils on the respective days after L. mexicana infection. Right, representative clinical course of C57BL/6 mice infected with L. mexicana and influx of SSC high CD11b + SiglecF + eosinophils as measured by flow cytometry ( n = 4 mice per group, 4 independent experiments). ( B ) Quantification of Il5 mRNA expression by qRT-PCR in L. mexicana -induced skin lesions of C57BL/6 mice (day 0 and day 20: n = 3 mice each; day 6 and day 14: n = 11 mice each; 1–3 independent experiments). ( C ) Bead-based multiplex ELISA of serum cytokines from C57BL/6 mice 14 days p.i. with L. mexicana ( n = 14 mice per group, 3–4 independent experiments). ( D ) Serum IL-5 levels measured by ELISA in C57BL/6 mice infected with L. mexicana (day 0: n = 3; day 6: n = 13; day 14: n = 12; day 20: n = 10; day 56: n = 5, 2–4 independent experiments). ( E ) Right, representative flow cytometric analysis of bone marrow and blood cells isolated from naive or L. mexicana -infected C57BL/6 mice. Left, quantification of the respective population and organ (left panel day 0 n = 5, day 6 n = 9, day 14 n = 11, and day 20 n = 6; middle panel day 0 n = 4, day 6 n = 8, day 14 n = 6, and day 20 n = 6; right panel day 0 n = 5, day 6 n = 10, day 14 n = 12, and day 20 n = 5, 1–3 independent experiments). ( F ) C57BL/6 mice were treated with 500 µg of either isotype control or anti-IL-5 antibody on days 5 and 12 p.i. Right, representative flow cytometric analysis of isolated cells from bone marrow, blood and skin lesions of isotype-treated or anti-IL-5-treated mice. Left, quantification of the respective population and organ (left panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; middle panel: day 0 n = 5, isotype n = 8, anti-IL-5 n = 8; right panel: day 0 n = 3, isotype n = 4, anti-IL-5 n = 4, 2 independent experiments; skin data points were derived from samples pooled from two mice). ( A , E ) Minor differences in gating between the time points reflect that samples were acquired on different experimental days based on the fact that mice were infected with the same parasite batch. Data are mean ± SEM ( A ) or mean ± s.d. ( B – F ). Information regarding the exact p values and the statistical tests performed is provided in the Appendix Table . .

Article Snippet: Il5 , Mm00439646_m1.

Techniques: Isolation, Infection, Flow Cytometry, Expressing, Quantitative RT-PCR, Multiplex Assay, Enzyme-linked Immunosorbent Assay, Control, Derivative Assay