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il 17f neutralizing antibody  (Bio X Cell)


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    Structured Review

    Bio X Cell il 17f neutralizing antibody
    Il 17f Neutralizing Antibody, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 94/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/il 17f neutralizing antibody/product/Bio X Cell
    Average 94 stars, based on 11 article reviews
    il 17f neutralizing antibody - by Bioz Stars, 2026-04
    94/100 stars

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    Figure 4. Effect of IL17 on angiotensin II–induced atherosclerosis and examination of <t>IL17F</t> levels. ApoE/ and IL17/ApoE/ mice were infused with angiotensin II for 4 weeks via osmotic minipump. Atherosclerotic lesions in the thoracic aortas were quantified by planimetry (A). Example aortas are shown on the left, and summary data are shown on the right (n7 per group; Pnot significant). Splenic lymphocytes from ApoE/ and IL17/ApoE/ mice fed regular (Reg) or high-fat (HF) diet for 3 months were cultured on anti- CD3 plates, and IL17F released into the media was measured by ELISA (B) (n5 to 7 per group). Data were analyzed using the Stu- dent’s t test. The statistical values in panel B represent a Bonferroni correction for 4 comparisons.
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    KEY RESOURCES TABLE

    Journal: Cancer cell

    Article Title: Dendritic cell paucity leads to dysfunctional immune surveillance in pancreatic cancer

    doi: 10.1016/j.ccell.2020.02.008

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: For cytokine depletion regimen, 400 μg each of IL-17A and IL-17F neutralizing antibodies (rat clone 17F3; clone MM17F8F5.1A9, BioXCell) or 250 μg of IFN-γ neutralizing antibodies (rat clone XMG1.2, BioXCell) were similarly administered (every 3-4 days) until 6-week timepoint was reached.

    Techniques: Recombinant, Cell Stimulation, Enzyme-linked Immunosorbent Assay, CyQUANT Assay, LDH Cytotoxicity Assay, Expressing, Staining, Derivative Assay, Software

    Figure 4. Effect of IL17 on angiotensin II–induced atherosclerosis and examination of IL17F levels. ApoE/ and IL17/ApoE/ mice were infused with angiotensin II for 4 weeks via osmotic minipump. Atherosclerotic lesions in the thoracic aortas were quantified by planimetry (A). Example aortas are shown on the left, and summary data are shown on the right (n7 per group; Pnot significant). Splenic lymphocytes from ApoE/ and IL17/ApoE/ mice fed regular (Reg) or high-fat (HF) diet for 3 months were cultured on anti- CD3 plates, and IL17F released into the media was measured by ELISA (B) (n5 to 7 per group). Data were analyzed using the Stu- dent’s t test. The statistical values in panel B represent a Bonferroni correction for 4 comparisons.

    Journal: Arteriosclerosis, Thrombosis, and Vascular Biology

    Article Title: Role of Interleukin 17 in Inflammation, Atherosclerosis, and Vascular Function in Apolipoprotein E–Deficient Mice

    doi: 10.1161/atvbaha.111.227629

    Figure Lengend Snippet: Figure 4. Effect of IL17 on angiotensin II–induced atherosclerosis and examination of IL17F levels. ApoE/ and IL17/ApoE/ mice were infused with angiotensin II for 4 weeks via osmotic minipump. Atherosclerotic lesions in the thoracic aortas were quantified by planimetry (A). Example aortas are shown on the left, and summary data are shown on the right (n7 per group; Pnot significant). Splenic lymphocytes from ApoE/ and IL17/ApoE/ mice fed regular (Reg) or high-fat (HF) diet for 3 months were cultured on anti- CD3 plates, and IL17F released into the media was measured by ELISA (B) (n5 to 7 per group). Data were analyzed using the Stu- dent’s t test. The statistical values in panel B represent a Bonferroni correction for 4 comparisons.

    Article Snippet: To examine a potential role of IL17F, IL17A/ApoE / were treated with anti-IL17F neutralization polyclonal antibody (100 g/mouse per injection, catalog no. AF2057, R&D Systems) or its isotype control (goat IgG, 100 g/mouse per injection, catalog no. AB-108-C, R&D Systems) once a week for 3 weeks starting 1 week before carotid ligation.

    Techniques: Cell Culture, Enzyme-linked Immunosorbent Assay