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rat anti mouse il 17e  (R&D Systems)


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    Structured Review

    R&D Systems rat anti mouse il 17e
    Rat Anti Mouse Il 17e, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat anti mouse il 17e/product/R&D Systems
    Average 92 stars, based on 4 article reviews
    rat anti mouse il 17e - by Bioz Stars, 2026-02
    92/100 stars

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    R&D Systems rat anti mouse il 25
    Wild type mice were injected with CL (1mg/kg body weight) for 2 (CL-2d) and 5 days (CL-5d), or were placed at controlled temperature (22°C) and cold challenge (4°C) in independently cages for 48h (n=4-5 per treatment). (A and F) The protein level of IL-17RB andUCP1 was analyzed by Western-blotin scWAT. HSP90 was used as a loading control. (B and G) Hematoxylin and eosin (H&E) staining of scWAT (400× magnification). (C and H) Immunohistochemical staining for UCP1of scWAT (400× magnification). (D and I) Immunofluorescent staining for <t>IL-25</t> (IL-25+ green) and UCP1 (UCP1 + red) or IL-17RB (IL-17RB+ red) of scWAT. Nucleus stained with DAPI (blue). Images were photographed at 200× magnification. (E and F) IL-25 protein expression in scWAT (E) or serum (J) (n=4-5 per treatment). *p < 0.05 by two-sided unpaired t-test. Data present as mean ± SEM.
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    ProSci Incorporated rat anti mouse il 17e monoclonal antibody
    Protein expression of IL-33, <t>IL-17E</t> and TSLP. Expression levels of IL-33, IL-17E and TSLP in the nasal mucosa of the mice in each group were determined by Western blotting.
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    Wild type mice were injected with CL (1mg/kg body weight) for 2 (CL-2d) and 5 days (CL-5d), or were placed at controlled temperature (22°C) and cold challenge (4°C) in independently cages for 48h (n=4-5 per treatment). (A and F) The protein level of IL-17RB andUCP1 was analyzed by Western-blotin scWAT. HSP90 was used as a loading control. (B and G) Hematoxylin and eosin (H&E) staining of scWAT (400× magnification). (C and H) Immunohistochemical staining for UCP1of scWAT (400× magnification). (D and I) Immunofluorescent staining for IL-25 (IL-25+ green) and UCP1 (UCP1 + red) or IL-17RB (IL-17RB+ red) of scWAT. Nucleus stained with DAPI (blue). Images were photographed at 200× magnification. (E and F) IL-25 protein expression in scWAT (E) or serum (J) (n=4-5 per treatment). *p < 0.05 by two-sided unpaired t-test. Data present as mean ± SEM.

    Journal: bioRxiv

    Article Title: IL-25 induces beige fat to improve metabolic homeostasis via macrophage and innervation

    doi: 10.1101/474288

    Figure Lengend Snippet: Wild type mice were injected with CL (1mg/kg body weight) for 2 (CL-2d) and 5 days (CL-5d), or were placed at controlled temperature (22°C) and cold challenge (4°C) in independently cages for 48h (n=4-5 per treatment). (A and F) The protein level of IL-17RB andUCP1 was analyzed by Western-blotin scWAT. HSP90 was used as a loading control. (B and G) Hematoxylin and eosin (H&E) staining of scWAT (400× magnification). (C and H) Immunohistochemical staining for UCP1of scWAT (400× magnification). (D and I) Immunofluorescent staining for IL-25 (IL-25+ green) and UCP1 (UCP1 + red) or IL-17RB (IL-17RB+ red) of scWAT. Nucleus stained with DAPI (blue). Images were photographed at 200× magnification. (E and F) IL-25 protein expression in scWAT (E) or serum (J) (n=4-5 per treatment). *p < 0.05 by two-sided unpaired t-test. Data present as mean ± SEM.

    Article Snippet: For immunofluorescence staining, slides were incubated with rabbit anti-mouse IL-17RB (1:1000; H-40, Santa Cruz), rabbit anti-mouse UCP1(1:1000; ab10983, Abcam) or rat anti-mouse IL-25 (1:1000; MAB1399, R&D) overnight at 4°C, followed by staining with a mixture of secondary antibodies containing an Alex Flour 488-Donkey anti-rat IgG (H+L) (1:200; A21208, Life Technologies) and an Alex Flour 594-Donkey anti-rabbit IgG (1:200; R37119, Life Technologies) for 1h at room temperature.

    Techniques: Injection, Western Blot, Staining, Immunohistochemical staining, Expressing

    Protein expression of IL-33, IL-17E and TSLP. Expression levels of IL-33, IL-17E and TSLP in the nasal mucosa of the mice in each group were determined by Western blotting.

    Journal: Experimental & Molecular Medicine

    Article Title: Downregulation of Orai1 expression in the airway alleviates murine allergic rhinitis

    doi: 10.3858/emm.2012.44.3.013

    Figure Lengend Snippet: Protein expression of IL-33, IL-17E and TSLP. Expression levels of IL-33, IL-17E and TSLP in the nasal mucosa of the mice in each group were determined by Western blotting.

    Article Snippet: The expressions of IL-33, IL-17E and TSLP were also analyzed using rat anti-mouse IL-33 monoclonal antibody (R&D systems, Minneapolis, MN), rat anti-mouse IL-17E monoclonal antibody (R&D systems), and rabbit anti-mouse TSLP polyclonal antibody (ProSci Incorporated, Poway, CA), respectively.

    Techniques: Expressing, Western Blot