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mouse inflammation cytokine antibody arrays  (R&D Systems)


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    R&D Systems mouse inflammation cytokine antibody arrays
    Mouse Inflammation Cytokine Antibody Arrays, supplied by R&D Systems, used in various techniques. Bioz Stars score: 96/100, based on 522 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cytokine+antibody+array/Proteome+Profiler+Mouse+XL+Cytokine+Array/bio_rxiv__64898__2026__02__24__707647-139-9-13
    Average 96 stars, based on 522 article reviews
    mouse inflammation cytokine antibody arrays - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Ab Array:

    Article Title: TRPV4 Activation Increases the Expression of CD207 (Langerin) of Monocyte-Derived Langerhans Cells without Affecting their Maturation.
    Article Snippet: Langerhans cells (LCs) are the sole professional antigen-presenting cell normally found in the human epidermal compartment.. Research into their physiological role is hindered by the fact that they are invariably activated during isolation from the skin.. To overcome this challenge, we turned to a monocyte-derived LC (moLC) model, which we characterized with RNA sequencing, and compared the transcriptome of moLCs with that of donor-matched immature dendritic cells.

    Article Title: Interleukin‐1β triggers muscle‐derived extracellular superoxide dismutase expression and protects muscles from doxorubicin‐induced atrophy
    Article Snippet: Immunoblots were analysed using ImageQuant LAS 500 (GE HealthCare Japan, Tokyo, Japan) and quantified using ImageJ software (US National Institutes of Health). .. Doxorubicin-treatedC2C12-culturedmediumandmouse serum were isolated and subjected to proteome profiling using a cytokine antibody array (ARY006; R&D Systems) according to the manufacturer’s instructions and previous studies (Okutsu et al., 2021; Yamada et al., 2018, 2019a). ..

    Article Title: Adipocyte metabolism is improved by TNF receptor-targeting small RNAs identified from dried nuts
    Article Snippet: Immunoreactive bands were detected by a FluorChem FC3 system (ProteinSimple, San Jose, CA, USA) after incubation of the membranes with ECL Selected Western Blotting Detection Reagent (GE Healthcare, Pittsburgh, PA, USA). .. Cytokine antibody array (R&D Systems Inc., Minneapolis, MN, USA) was used to detect the cytokine protein levels in 200 μg of a pool of total homogenate obtained from murine visceral adipose tissue. ..

    Article Title: Breast Cancer Stem Cells Secrete MIF to Mediate Tumor Metabolic Reprogramming That Drives Immune Evasion
    Article Snippet: 36 Reprogramming of energy metabolism exerts pivotal functions in cancer 37 progression and immune surveillance.. Identification of the mechanisms mediating 38 metabolic changes in cancer may lead to improved strategies to suppress tumor 39 growth and stimulate anti-tumor immunity.. Here, it was observed that the secretomes 40 of hypoxic breast cancer cells and breast cancer stem cells (BCSCs) induced 41 reprogramming of metabolic pathways, particularly glycolysis, in normoxic breast 42 cancer cells.

    Article Title: Glycolysis reprogramming in CAFs promotes oxaliplatin resistance in pancreatic cancer through circABCC4 mediated PKM2 nuclear translocation
    Article Snippet: The PARIS kit (AM1921, Thermo Scientific, USA) was used to separate the CAFs’ cytoplasmic and nuclear RNAs and protein according to the manufacturer’s protocol. .. A cytokine antibody array was performed using the Proteome Profiler Human XL Cytokine Array Kit (ARY022B, R&D Systems, USA). ..

    Article Title: Drug for treating corneal endothelium by promoting cell proliferation or inhibiting cell damage
    Article Snippet: .. Based on the aforementioned experimental methodology, a cytokine antibody array (Proteome Profiler, # ARY005, R&D Systems) blotted with 36 types of antibodies was used to find the expression pattern of cytokines in a human corneal endothelial culture solution. ..

    Article Title: Cancer-associated fibroblasts induce epithelial–mesenchymal transition of breast cancer cells through paracrine TGF- β signalling
    Article Snippet: .. The TGF β s secreted from CAFs were analysed using a Cytokine Antibody Array (R&D Systems) in accordance with the manufacturer's instructions. ..

    Isolation:

    Article Title: Interleukin‐1β triggers muscle‐derived extracellular superoxide dismutase expression and protects muscles from doxorubicin‐induced atrophy
    Article Snippet: Immunoblots were analysed using ImageQuant LAS 500 (GE HealthCare Japan, Tokyo, Japan) and quantified using ImageJ software (US National Institutes of Health). .. Doxorubicin-treatedC2C12-culturedmediumandmouse serum were isolated and subjected to proteome profiling using a cytokine antibody array (ARY006; R&D Systems) according to the manufacturer’s instructions and previous studies (Okutsu et al., 2021; Yamada et al., 2018, 2019a). ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Breast Cancer Stem Cells Secrete MIF to Mediate Tumor Metabolic Reprogramming That Drives Immune Evasion
    Article Snippet: 36 Reprogramming of energy metabolism exerts pivotal functions in cancer 37 progression and immune surveillance.. Identification of the mechanisms mediating 38 metabolic changes in cancer may lead to improved strategies to suppress tumor 39 growth and stimulate anti-tumor immunity.. Here, it was observed that the secretomes 40 of hypoxic breast cancer cells and breast cancer stem cells (BCSCs) induced 41 reprogramming of metabolic pathways, particularly glycolysis, in normoxic breast 42 cancer cells.

    Expressing:

    Article Title: Drug for treating corneal endothelium by promoting cell proliferation or inhibiting cell damage
    Article Snippet: .. Based on the aforementioned experimental methodology, a cytokine antibody array (Proteome Profiler, # ARY005, R&D Systems) blotted with 36 types of antibodies was used to find the expression pattern of cytokines in a human corneal endothelial culture solution. ..



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    R&D Systems rat cytokine antibody arrays
    HBOT reduces gingival <t>cytokine</t> and chemokine expression in ligature-induced periodontitis. (A) Representative cytokine array blots showing expression profiles of 10 key inflammatory mediators (red boxes) in gingival tissues collected at day 14 and day 28 from Sham, PD+RECOV (natural recovery), PD (periodontitis only), PD+EHBOT (early HBOT), and PD+LHBOT (late HBOT) groups. The targeted proteins included: 1. CINC-1 (CXCL1), 2. CINC-2α/β (CXCL3), 3. sICAM-1, 4. IL-1α, 5. IL-1β, 6. IL-1 receptor antagonist (IL-1ra), 7. LIX (CXCL5), 8. L-selectin (CD62L), 9. Thymus chemokine (CCL25), and 10. TIMP-1. (B) Quantitative analysis of cytokine and chemokine expression at day 14. Periodontitis induced marked increases in several pro-inflammatory cytokines and chemokines. Early HBOT significantly suppressed most inflammatory mediators compared to the PD and PD+RECOV groups. (C) Quantitative analysis at day 28. PD-induced cytokine elevation persisted, while both early and late HBOT treatments effectively reduced IL-1α, IL-1β, IL-1ra, sICAM-1, CINC-1, CINC-2α/β, LIX, and thymus chemokine levels. Notably, early HBOT more effectively reduced thymus chemokine expression than natural recovery. Data are presented as mean ± SD. n = 6 per group. Panel 2A shows a cytokine dot-array membrane (R&D <t>Systems</t> <t>ARY008)</t> from a single, intact exposure; the published panel was border-cropped only to remove blank margins (global linear contrast, no compositing). See Supplementary for the full, uncropped membrane and original X-film/RAW.
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    R&D Systems antibody based protein array
    HBOT reduces gingival <t>cytokine</t> and chemokine expression in ligature-induced periodontitis. (A) Representative cytokine array blots showing expression profiles of 10 key inflammatory mediators (red boxes) in gingival tissues collected at day 14 and day 28 from Sham, PD+RECOV (natural recovery), PD (periodontitis only), PD+EHBOT (early HBOT), and PD+LHBOT (late HBOT) groups. The targeted proteins included: 1. CINC-1 (CXCL1), 2. CINC-2α/β (CXCL3), 3. sICAM-1, 4. IL-1α, 5. IL-1β, 6. IL-1 receptor antagonist (IL-1ra), 7. LIX (CXCL5), 8. L-selectin (CD62L), 9. Thymus chemokine (CCL25), and 10. TIMP-1. (B) Quantitative analysis of cytokine and chemokine expression at day 14. Periodontitis induced marked increases in several pro-inflammatory cytokines and chemokines. Early HBOT significantly suppressed most inflammatory mediators compared to the PD and PD+RECOV groups. (C) Quantitative analysis at day 28. PD-induced cytokine elevation persisted, while both early and late HBOT treatments effectively reduced IL-1α, IL-1β, IL-1ra, sICAM-1, CINC-1, CINC-2α/β, LIX, and thymus chemokine levels. Notably, early HBOT more effectively reduced thymus chemokine expression than natural recovery. Data are presented as mean ± SD. n = 6 per group. Panel 2A shows a cytokine dot-array membrane (R&D <t>Systems</t> <t>ARY008)</t> from a single, intact exposure; the published panel was border-cropped only to remove blank margins (global linear contrast, no compositing). See Supplementary for the full, uncropped membrane and original X-film/RAW.
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    Image Search Results


    HBOT reduces gingival cytokine and chemokine expression in ligature-induced periodontitis. (A) Representative cytokine array blots showing expression profiles of 10 key inflammatory mediators (red boxes) in gingival tissues collected at day 14 and day 28 from Sham, PD+RECOV (natural recovery), PD (periodontitis only), PD+EHBOT (early HBOT), and PD+LHBOT (late HBOT) groups. The targeted proteins included: 1. CINC-1 (CXCL1), 2. CINC-2α/β (CXCL3), 3. sICAM-1, 4. IL-1α, 5. IL-1β, 6. IL-1 receptor antagonist (IL-1ra), 7. LIX (CXCL5), 8. L-selectin (CD62L), 9. Thymus chemokine (CCL25), and 10. TIMP-1. (B) Quantitative analysis of cytokine and chemokine expression at day 14. Periodontitis induced marked increases in several pro-inflammatory cytokines and chemokines. Early HBOT significantly suppressed most inflammatory mediators compared to the PD and PD+RECOV groups. (C) Quantitative analysis at day 28. PD-induced cytokine elevation persisted, while both early and late HBOT treatments effectively reduced IL-1α, IL-1β, IL-1ra, sICAM-1, CINC-1, CINC-2α/β, LIX, and thymus chemokine levels. Notably, early HBOT more effectively reduced thymus chemokine expression than natural recovery. Data are presented as mean ± SD. n = 6 per group. Panel 2A shows a cytokine dot-array membrane (R&D Systems ARY008) from a single, intact exposure; the published panel was border-cropped only to remove blank margins (global linear contrast, no compositing). See Supplementary for the full, uncropped membrane and original X-film/RAW.

    Journal: International Journal of Medical Sciences

    Article Title: Hyperbaric oxygen protects against periodontal bone loss by modulating inflammation and bone remodeling via RANKL/OPG expression in ligature-induced periodontitis

    doi: 10.7150/ijms.122857

    Figure Lengend Snippet: HBOT reduces gingival cytokine and chemokine expression in ligature-induced periodontitis. (A) Representative cytokine array blots showing expression profiles of 10 key inflammatory mediators (red boxes) in gingival tissues collected at day 14 and day 28 from Sham, PD+RECOV (natural recovery), PD (periodontitis only), PD+EHBOT (early HBOT), and PD+LHBOT (late HBOT) groups. The targeted proteins included: 1. CINC-1 (CXCL1), 2. CINC-2α/β (CXCL3), 3. sICAM-1, 4. IL-1α, 5. IL-1β, 6. IL-1 receptor antagonist (IL-1ra), 7. LIX (CXCL5), 8. L-selectin (CD62L), 9. Thymus chemokine (CCL25), and 10. TIMP-1. (B) Quantitative analysis of cytokine and chemokine expression at day 14. Periodontitis induced marked increases in several pro-inflammatory cytokines and chemokines. Early HBOT significantly suppressed most inflammatory mediators compared to the PD and PD+RECOV groups. (C) Quantitative analysis at day 28. PD-induced cytokine elevation persisted, while both early and late HBOT treatments effectively reduced IL-1α, IL-1β, IL-1ra, sICAM-1, CINC-1, CINC-2α/β, LIX, and thymus chemokine levels. Notably, early HBOT more effectively reduced thymus chemokine expression than natural recovery. Data are presented as mean ± SD. n = 6 per group. Panel 2A shows a cytokine dot-array membrane (R&D Systems ARY008) from a single, intact exposure; the published panel was border-cropped only to remove blank margins (global linear contrast, no compositing). See Supplementary for the full, uncropped membrane and original X-film/RAW.

    Article Snippet: Protein extracts (200 μg per sample) were applied to Rat Cytokine Antibody Arrays (ARY008, R&D Systems, Inc., USA), which detect a panel of 34 inflammatory cytokines, chemokines, and adhesion molecules.

    Techniques: Expressing, Membrane