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anti il17f neutralization polyclonal antibody  (R&D Systems)


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    R&D Systems anti il17f neutralization polyclonal antibody
    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.
    Anti Il17f Neutralization Polyclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+il17f+neutralization+polyclonal+antibody/10__1161_slash_atvbaha__111__227629-43-12-23?v=R%26D+Systems
    Average 90 stars, based on 7 article reviews
    anti il17f neutralization polyclonal antibody - by Bioz Stars, 2026-08
    90/100 stars

    Images

    1) Product Images from "Role of Interleukin 17 in Inflammation, Atherosclerosis, and Vascular Function in Apolipoprotein E–Deficient Mice"

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

    Journal: Arteriosclerosis, Thrombosis, and Vascular Biology

    doi: 10.1161/atvbaha.111.227629

    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.
    Figure Legend 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.

    Techniques Used: Cell Culture, Enzyme-linked Immunosorbent Assay



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    anti il17f neutralization polyclonal antibody  (R&D Systems)
    90
    R&D Systems anti il17f neutralization polyclonal antibody
    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.
    Anti Il17f Neutralization Polyclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+il17f+neutralization+polyclonal+antibody/10__1161_slash_atvbaha__111__227629-43-12-23?v=R%26D+Systems
    Average 90 stars, based on 1 article reviews
    anti il17f neutralization polyclonal antibody - by Bioz Stars, 2026-08
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    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