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ccl21  (R&D Systems)


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    Structured Review

    R&D Systems ccl21
    Ccl21, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ccl21/Human+CCL21%2F6Ckine+DuoSet+ELISA/pm42775509-140-9-24
    Average 93 stars, based on 13 article reviews
    ccl21 - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    other:

    Article Title: Table 1
    Article Snippet: CCL21 , AF366 , Polyclonal Goat IgG , Unconjugated , 1/100 , R&D Systems.

    Article Title: Table 1
    Article Snippet: CCL21 , AF457 , Polyclonal Goat IgG , Unconjugated , 1/50 , R&D Systems.

    Injection:

    Article Title: Modulating activated fibroblastic reticular cells within lymph nodes to boost nanovaccine efficacy in hepatocellular carcinoma
    Article Snippet: .. The orthotopic Hepa1-6 tumor-bearing mice at 14 days after inoc- ulation were intraperitoneally injected with or without anti-mouse CCL19 antibody (10 μg, AF880, R&D Systems) or CCL21-blocking antibody (10 μg, AF457, R&D Systems) twice with a 2-day interval. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Lymphatic Endothelial Senescence Is Associated with Drainage Failure Despite Vessel Expansion in Pulmonary Fibrosis.
    Article Snippet: Cells were 383 then washed with PBS and maintained in fresh endothelial basal medium (Cat. 384 No. cAP-03; Angio-Proteomie) for an additional 24 hours. .. Conditioned media 385 were collected, and the concentrations of CCL21 and MIF in cell-free 386 supernatants were measured using human CCL21 (Cat. No. DY366; R&D 387 Systems) and MIF (Cat. No. DMF00B; R&D Systems) ELISA kits, respectively. ..

    Staining:

    Article Title: The thrombin receptor PAR1 orchestrates changes in lymphatic endothelial cell junction morphology to augment lymphatic drainage during lung injury
    Article Snippet: .. Slides from paraffin-embedded sections were stained with hematoxylin and eosin or immunostained as described previously , with the following antibodies: VEGFR3 (1:50 dilution, catalogue number AF743, R&D Systems); CCL21 (1:50 dilution, catalogue number AF457, R&D Systems); or RFP (1:100 dilution, catalogue number 600401379S, Rockland). .. Immunofluorescence was performed using a Nikon Eclipse microscope (×20 objective) with the NIS-Elements software.

    Immunofluorescence:

    Article Title: CXCL9, CXCL10, and CCL19 synergistically recruit T lymphocytes to skin in lichen planus
    Article Snippet: .. For immunofluorescence microscopy, the following antibodies were used: CD3 (MCA1477, Bio-Rad), CD4 + (ab183685, Abcam), CXCL13 (AF801, R&D Biosystems), CXCL9 (ab9720, Abcam), CCL19 (PA5-109488, Thermo Fisher Scientific), and CCL21 (AF366, R&D Biosystems). .. The scRNA sequencing data were mapped to the GRCh38 reference genome to generate gene count and cell barcode matrices using the “cellranger count” function from the cellranger pipeline (version 5.0.1, 10X Genomics).

    Article Title: CXCL9, CXCL10, and CCL19 synergistically recruit T lymphocytes to skin in lichen planus.
    Article Snippet: .. For immunofluorescence microscopy, the following antibodies were used: CD3 (MCA1477, BioRad), CD4 (ab183685, Abcam), CXCL13 (AF801, R&D Biosystem), CXCL9 (ab9720, Abcam), CCL19 (PA5-109488, ThermoFisher Scientific), and CCL21 (AF366, R&D Biosystem). .. scRNA-seq Data analysis The scRNA sequencing data was mapped to the GRCh38 reference genome to generate gene count and cell barcode matrices using the “cellranger count” function from the cellranger pipeline (version 5.0.1, 10X Genomics).

    Microscopy:

    Article Title: CXCL9, CXCL10, and CCL19 synergistically recruit T lymphocytes to skin in lichen planus
    Article Snippet: .. For immunofluorescence microscopy, the following antibodies were used: CD3 (MCA1477, Bio-Rad), CD4 + (ab183685, Abcam), CXCL13 (AF801, R&D Biosystems), CXCL9 (ab9720, Abcam), CCL19 (PA5-109488, Thermo Fisher Scientific), and CCL21 (AF366, R&D Biosystems). .. The scRNA sequencing data were mapped to the GRCh38 reference genome to generate gene count and cell barcode matrices using the “cellranger count” function from the cellranger pipeline (version 5.0.1, 10X Genomics).

    Article Title: CXCL9, CXCL10, and CCL19 synergistically recruit T lymphocytes to skin in lichen planus.
    Article Snippet: .. For immunofluorescence microscopy, the following antibodies were used: CD3 (MCA1477, BioRad), CD4 (ab183685, Abcam), CXCL13 (AF801, R&D Biosystem), CXCL9 (ab9720, Abcam), CCL19 (PA5-109488, ThermoFisher Scientific), and CCL21 (AF366, R&D Biosystem). .. scRNA-seq Data analysis The scRNA sequencing data was mapped to the GRCh38 reference genome to generate gene count and cell barcode matrices using the “cellranger count” function from the cellranger pipeline (version 5.0.1, 10X Genomics).

    Sterility:




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    Image Search Results


    A Experimental design. Primary human CD8⁺ T cells were co-engineered with a lentiviral construct encoding the NR4A2-responsive synthetic promoter SP73 driving mCherry and constitutive EGFP to identify transduced cells, together with a retroviral NY-ESO-1–specific TCR. Engineered T cells were expanded and co-cultured with NY-ESO-1–expressing SK-MEL23 melanoma cells. B Quantification of mCherry⁺ T cells over time during co-culture. SP73-engineered T cells show progressive reporter induction, whereas control cells transduced with the control promoter SP01 (lacking NR4A2 binding sites) remain at baseline levels. Data represent mean ± SEM of n = 3 independent donors. C Representative IncuCyte® live-cell images showing SP73-driven mCherry fluorescence during co-culture with SK-MEL23 melanoma cells; SP01 controls show negligible signal. D Expression of NR4A2 and activation/dysfunction-associated markers in engineered T cells during co-culture. Data represent mean ± SEM of n = 3 independent biological donors. Statistical analysis was performed using one-way ANOVA with Tukey’s post hoc test. P values: CD39, P < 0.0001 for R0vsR2 and R0vsR4, P = 0.0048 for R2vsR4. NR4A2, P = 0.0375 for R0vsR2. LAG-3, P = 0.0194 for R0vsR2, P = 0.0097 for R0vsR4. TIM-3, P = 0.008 for R0vsR2, P = 0.0433 for R2vsR4. TIGIT, P = 0.0082 for R0vsR4, P = 0.0433 for R2vsR4. E Functional assessment of engineered T cells prior co-culture (R0) and following persistent antigen exposure (R4). Left: Quantification of IL-2⁺, TNFα⁺, CD107a⁺, and IFNγ⁺ cells following Leukocyte Activation Cocktail (LAC) stimulation. Right: Representative flow cytometry histograms illustrating shifts in cytokine-producing populations. Data represent mean ± SEM of n = 3 independent biological donors. Statistical analysis was performed using a two-tailed paired t test comparing R0 vs R4. P values: IL-2, P = 0.0074; TNFα, P = 0.0068; CD107a, P = 0.0401; IFNγ, P = 0.0147. Source data for this figure is available in the  file. Created in BioRender.

    Journal: Nature Communications

    Article Title: A modular synthetic promoter toolkit for programmable gene control in activated and chronically stimulated T cells

    doi: 10.1038/s41467-026-77730-7

    Figure Lengend Snippet: A Experimental design. Primary human CD8⁺ T cells were co-engineered with a lentiviral construct encoding the NR4A2-responsive synthetic promoter SP73 driving mCherry and constitutive EGFP to identify transduced cells, together with a retroviral NY-ESO-1–specific TCR. Engineered T cells were expanded and co-cultured with NY-ESO-1–expressing SK-MEL23 melanoma cells. B Quantification of mCherry⁺ T cells over time during co-culture. SP73-engineered T cells show progressive reporter induction, whereas control cells transduced with the control promoter SP01 (lacking NR4A2 binding sites) remain at baseline levels. Data represent mean ± SEM of n = 3 independent donors. C Representative IncuCyte® live-cell images showing SP73-driven mCherry fluorescence during co-culture with SK-MEL23 melanoma cells; SP01 controls show negligible signal. D Expression of NR4A2 and activation/dysfunction-associated markers in engineered T cells during co-culture. Data represent mean ± SEM of n = 3 independent biological donors. Statistical analysis was performed using one-way ANOVA with Tukey’s post hoc test. P values: CD39, P < 0.0001 for R0vsR2 and R0vsR4, P = 0.0048 for R2vsR4. NR4A2, P = 0.0375 for R0vsR2. LAG-3, P = 0.0194 for R0vsR2, P = 0.0097 for R0vsR4. TIM-3, P = 0.008 for R0vsR2, P = 0.0433 for R2vsR4. TIGIT, P = 0.0082 for R0vsR4, P = 0.0433 for R2vsR4. E Functional assessment of engineered T cells prior co-culture (R0) and following persistent antigen exposure (R4). Left: Quantification of IL-2⁺, TNFα⁺, CD107a⁺, and IFNγ⁺ cells following Leukocyte Activation Cocktail (LAC) stimulation. Right: Representative flow cytometry histograms illustrating shifts in cytokine-producing populations. Data represent mean ± SEM of n = 3 independent biological donors. Statistical analysis was performed using a two-tailed paired t test comparing R0 vs R4. P values: IL-2, P = 0.0074; TNFα, P = 0.0068; CD107a, P = 0.0401; IFNγ, P = 0.0147. Source data for this figure is available in the file. Created in BioRender.

    Article Snippet: The sequence of IL12p70 was obtained from pLN540 (FuGW-G8p-IL12-P2A-CCL21-1Pe) (Addgene #105201 ).

    Techniques: Construct, Retroviral, Cell Culture, Expressing, Co-culture Assay, Control, Transduction, Binding Assay, Fluorescence, Activation Assay, Analysis, Functional Assay, Flow Cytometry, Two Tailed Test