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rat anti mhc ii  (R&D Systems)


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    Structured Review

    R&D Systems rat anti mhc ii
    Rat Anti Mhc Ii, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 93 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat anti mhc ii/product/R&D Systems
    Average 93 stars, based on 93 article reviews
    rat anti mhc ii - by Bioz Stars, 2026-03
    93/100 stars

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    R&D Systems anti-mouse ccl21 antibody
    A Measurement of chemokine concentrations in peripheral lymph nodes from psoriatic mice (n = 5). B Relative Ccl21a expression in different tissues of psoriatic mice (n = 5). Significant differences in comparison with lymph nodes. C Representative images and quantification of MSC recruited by the homogenate of lymph node from psoriatic mice in the presence of <t>anti-CCL21</t> antibody (n = 5). D Illustration of the scheme depicting MSC treatment for psoriatic mice pretreated with <t>anti-CCL21</t> antibody. E Quantification of MSC in the peripheral lymph nodes of psoriatic mice pretreated with anti-CCL21 antibody 24 h after MSC administration (n = 5). F In vivo IVIM imaging of MSC-RFP in inguinal lymph nodes from psoriatic mice pretreated with anti-CCL21 antibody. Scale bar, 100 μm. G Immunofluorescence colocalization analysis of CCL21 with high endothelial cells (MECA-79) or lymphatic endothelial cells (LYVE) in the peripheral lymph nodes of normal mice and psoriatic mice. Scale bars, 100 μm. H Secreted protein levels of CCL21 in SVEC-10 cells stimulated with lymph node homogenate for 16 h were analyzed 8 h after media refreshment (n = 5). I Quantification of MSC recruited in a transwell culture system by conditioned medium collected after the stimulation of SVEC4-10 cells with lymph node homogenate for 16 h (n = 5). J CCR7 expression in MSC stimulated with mouse serum for 24 h was determined by flow cytometry (n = 5). The data are presented as the means ± SEMs. *P < 0.05, ** P < 0.01 and *** P < 0.001.
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    R&D Systems goat anti mouse ccl21
    A Measurement of chemokine concentrations in peripheral lymph nodes from psoriatic mice (n = 5). B Relative Ccl21a expression in different tissues of psoriatic mice (n = 5). Significant differences in comparison with lymph nodes. C Representative images and quantification of MSC recruited by the homogenate of lymph node from psoriatic mice in the presence of <t>anti-CCL21</t> antibody (n = 5). D Illustration of the scheme depicting MSC treatment for psoriatic mice pretreated with <t>anti-CCL21</t> antibody. E Quantification of MSC in the peripheral lymph nodes of psoriatic mice pretreated with anti-CCL21 antibody 24 h after MSC administration (n = 5). F In vivo IVIM imaging of MSC-RFP in inguinal lymph nodes from psoriatic mice pretreated with anti-CCL21 antibody. Scale bar, 100 μm. G Immunofluorescence colocalization analysis of CCL21 with high endothelial cells (MECA-79) or lymphatic endothelial cells (LYVE) in the peripheral lymph nodes of normal mice and psoriatic mice. Scale bars, 100 μm. H Secreted protein levels of CCL21 in SVEC-10 cells stimulated with lymph node homogenate for 16 h were analyzed 8 h after media refreshment (n = 5). I Quantification of MSC recruited in a transwell culture system by conditioned medium collected after the stimulation of SVEC4-10 cells with lymph node homogenate for 16 h (n = 5). J CCR7 expression in MSC stimulated with mouse serum for 24 h was determined by flow cytometry (n = 5). The data are presented as the means ± SEMs. *P < 0.05, ** P < 0.01 and *** P < 0.001.
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    Image Search Results


    A Measurement of chemokine concentrations in peripheral lymph nodes from psoriatic mice (n = 5). B Relative Ccl21a expression in different tissues of psoriatic mice (n = 5). Significant differences in comparison with lymph nodes. C Representative images and quantification of MSC recruited by the homogenate of lymph node from psoriatic mice in the presence of anti-CCL21 antibody (n = 5). D Illustration of the scheme depicting MSC treatment for psoriatic mice pretreated with anti-CCL21 antibody. E Quantification of MSC in the peripheral lymph nodes of psoriatic mice pretreated with anti-CCL21 antibody 24 h after MSC administration (n = 5). F In vivo IVIM imaging of MSC-RFP in inguinal lymph nodes from psoriatic mice pretreated with anti-CCL21 antibody. Scale bar, 100 μm. G Immunofluorescence colocalization analysis of CCL21 with high endothelial cells (MECA-79) or lymphatic endothelial cells (LYVE) in the peripheral lymph nodes of normal mice and psoriatic mice. Scale bars, 100 μm. H Secreted protein levels of CCL21 in SVEC-10 cells stimulated with lymph node homogenate for 16 h were analyzed 8 h after media refreshment (n = 5). I Quantification of MSC recruited in a transwell culture system by conditioned medium collected after the stimulation of SVEC4-10 cells with lymph node homogenate for 16 h (n = 5). J CCR7 expression in MSC stimulated with mouse serum for 24 h was determined by flow cytometry (n = 5). The data are presented as the means ± SEMs. *P < 0.05, ** P < 0.01 and *** P < 0.001.

    Journal: Cell Death & Disease

    Article Title: Mesenchymal stromal cells restrain the Th17 cell response via L-amino-acid oxidase within lymph nodes

    doi: 10.1038/s41419-024-07024-7

    Figure Lengend Snippet: A Measurement of chemokine concentrations in peripheral lymph nodes from psoriatic mice (n = 5). B Relative Ccl21a expression in different tissues of psoriatic mice (n = 5). Significant differences in comparison with lymph nodes. C Representative images and quantification of MSC recruited by the homogenate of lymph node from psoriatic mice in the presence of anti-CCL21 antibody (n = 5). D Illustration of the scheme depicting MSC treatment for psoriatic mice pretreated with anti-CCL21 antibody. E Quantification of MSC in the peripheral lymph nodes of psoriatic mice pretreated with anti-CCL21 antibody 24 h after MSC administration (n = 5). F In vivo IVIM imaging of MSC-RFP in inguinal lymph nodes from psoriatic mice pretreated with anti-CCL21 antibody. Scale bar, 100 μm. G Immunofluorescence colocalization analysis of CCL21 with high endothelial cells (MECA-79) or lymphatic endothelial cells (LYVE) in the peripheral lymph nodes of normal mice and psoriatic mice. Scale bars, 100 μm. H Secreted protein levels of CCL21 in SVEC-10 cells stimulated with lymph node homogenate for 16 h were analyzed 8 h after media refreshment (n = 5). I Quantification of MSC recruited in a transwell culture system by conditioned medium collected after the stimulation of SVEC4-10 cells with lymph node homogenate for 16 h (n = 5). J CCR7 expression in MSC stimulated with mouse serum for 24 h was determined by flow cytometry (n = 5). The data are presented as the means ± SEMs. *P < 0.05, ** P < 0.01 and *** P < 0.001.

    Article Snippet: To neutralizing CCL21, mice received 10 μg of anti-mouse CCL21 antibody or control IgG (R&D System, Minneapolis, MN) 16 h before MSC infusion.

    Techniques: Expressing, Comparison, In Vivo, Imaging, Immunofluorescence, Flow Cytometry

    In mice with autoimmune diseases, elevated CCL21 levels drive the specific homing of MSC to lymph nodes following transplantation. Within the lymph nodes, MSC respond to TNF-α stimulation by secreting LAAO via NF-κB activation. LAAO catalyzes the production of I3P from tryptophan, which exhibits strong inhibitory effects on Th17 cells by activating the AHR pathway. The figure was created with BioRender ( https://biorender.com ).

    Journal: Cell Death & Disease

    Article Title: Mesenchymal stromal cells restrain the Th17 cell response via L-amino-acid oxidase within lymph nodes

    doi: 10.1038/s41419-024-07024-7

    Figure Lengend Snippet: In mice with autoimmune diseases, elevated CCL21 levels drive the specific homing of MSC to lymph nodes following transplantation. Within the lymph nodes, MSC respond to TNF-α stimulation by secreting LAAO via NF-κB activation. LAAO catalyzes the production of I3P from tryptophan, which exhibits strong inhibitory effects on Th17 cells by activating the AHR pathway. The figure was created with BioRender ( https://biorender.com ).

    Article Snippet: To neutralizing CCL21, mice received 10 μg of anti-mouse CCL21 antibody or control IgG (R&D System, Minneapolis, MN) 16 h before MSC infusion.

    Techniques: Transplantation Assay, Activation Assay