mouse il 11 levels Search Results


il 11 antagonist  (R&D Systems)
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Il 11 Antagonist, 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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rat r d systems mab418 pdgfrß  (R&D Systems)
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goat biotinylated antibody anti il11  (R&D Systems)
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Goat Biotinylated Antibody Anti Il11, 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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mouse monoclonal il11 antibody  (R&D Systems)
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R&D Systems mouse monoclonal il11 antibody
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Mouse Monoclonal Il11 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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recombinant mouse il 11 protein  (R&D Systems)
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R&D Systems recombinant mouse il 11 protein
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Recombinant Mouse Il 11 Protein, 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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murine il 11r antibody  (R&D Systems)
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R&D Systems murine il 11r antibody
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Murine Il 11r Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse recombinant il 1β  (R&D Systems)
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Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Mouse Recombinant Il 1β, 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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anti il 11  (R&D Systems)
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R&D Systems anti il 11
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Anti Il 11, supplied by R&D Systems, 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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biotinylated il 11r fc  (R&D Systems)
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R&D Systems biotinylated il 11r fc
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Biotinylated Il 11r Fc, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse il 1β duoset elisa  (R&D Systems)
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R&D Systems mouse il 1β duoset elisa
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
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mouse il 11 duoset elisa kit  (R&D Systems)
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R&D Systems mouse il 11 duoset elisa kit
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Mouse Il 11 Duoset Elisa Kit, 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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recombinant mouse il 11 rα fc chimera  (R&D Systems)
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R&D Systems recombinant mouse il 11 rα fc chimera
Figure 1 Immunohistochemical analysis of <t>IL11</t> expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 <t>MAB</t> (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.
Recombinant Mouse Il 11 Rα Fc Chimera, 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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Image Search Results


Figure 1 Immunohistochemical analysis of IL11 expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 MAB (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.

Journal: REPRODUCTION

Article Title: Preeclampsia-related increase of interleukin-11 expression in human decidual cells

doi: 10.1530/rep-10-0263

Figure Lengend Snippet: Figure 1 Immunohistochemical analysis of IL11 expression in control and preeclamptic decidua. Representative micrographs of serial sections from control (A–C) and preeclamptic (D–F) specimens are shown. Vimentin immunostaining (red) identifies decidual cells in control (A) and preeclamptic (D) tissues. Cytokeratin immunostaining (red) identifies trophoblastic cells in control (C) and preeclamptic (F) tissues. IL11 immunostaining (brown) in decidual cells (arrows) was cytoplasmic and more intense than in interstitial trophoblast (arrowheads), where IL11 localization was mostly perimembranous (E inset). Between groups, IL11 immunostaining was greater in preeclamptic (E) versus control (B) decidual cells, while there was no significant difference among interstitial trophoblast. IL11 intensity HSCOREs in control and preeclamptic specimens (meanGS.E.M.) are shown (K); *, versus control decidual cells; †, versus group-respective decidual cells; P!0.05. Additionally, no statistical significance for IL11 HSCOREs was observed between chorionic villi of preeclamptic and control tissues (G and H). On the other hand, no significant difference was found for the IL11R expression between preeclamptic (J) versus control interstitial cytotrophoblasts (I). Parallel staining with a mouse isotype was used as a negative control for IL11 MAB (C and G; inset). Note that IL11 immunoreactivity in interstitial trophoblast was mostly perimembranous, especially in preeclampsia specimens (E, inset). The scale bar in panel F represents 50 mm for all panels, except the panel E inset, where it represents 20 mm.

Article Snippet: Excess serum was then removed, and serial sections were incubated with either mouse monoclonal IL11 antibody (R&D Systems, Minneapolis, MN, USA) at 10 mg/ml in 1% blocking horse serum in TBS, or monoclonal IL11R antibody (R&D Systems) at 10 mg/ml in 1% blocking horse serum in TBS, or mouse monoclonal anti-vimentin antibody (DakoCytomation, Carpinteria, CA, USA) at 1:100 dilution in TBS, or anti-cytokeratin antibody (DakoCytomation) at 1:100 dilution in TBS overnight in a humidified chamber at C4 8C.

Techniques: Immunohistochemical staining, Expressing, Control, Immunostaining, Staining, Negative Control