IL-17F Antibodies
We offer IL-17F Antibodies for use in common research applications: ELISA, ELISA Capture (Matched Antibody Pair), ELISA Detection (Matched Antibody Pair), ELISA Standard (Matched Pair), Flow (Intracellular), Flow Cytometry, Immunocytochemistry, Immunohistochemistry, Immunohistochemistry-Paraffin, Intracellular Staining by Flow Cytometry, Neutralization, Sandwich ELISA, Western Blot. Each IL-17F Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our IL-17F Antibodies can be used in a variety of model species: Human, Mouse, Primate, Rat. Use the list below to choose the IL-17F Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our IL-17F polyclonal antibodies and browse our IL-17F monoclonal antibody catalog.
Alternate Names for IL-17F Antibodies
anti-IL-17F antibody, anti-IL17F antibody, anti-Cytokine ML-1 antibody, anti-IL-17Finterleukin-17F antibody, anti-IL-24 antibody, anti-IL24 antibody, anti-interleukin 17F antibody, anti-Interleukin-24 antibody, anti-ML-1 antibody, anti-ML1interleukin-24 antibody
45 Results for "il-17f" in Primary Antibodies
![Flow Cytometry: IL-17F Antibody (8F5.1A9) - Chimeric [NBP3-12034] - Mouse splenocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of 8F5.1A9 (NBP3-12034, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.](http://images.novusbio.com/fullsize/IL-17F-Antibody-8F5-1A9-Chimeric-Flow-Cytometry-NBP3-12034-img0001.jpg "Flow Cytometry: IL-17F Antibody (8F5.1A9) - Chimeric [NBP3-12034] - Mouse splenocytes were stimulated with PMA and Ionomycin in presence of Monensin for 4 hours. The cells were fixed using 2% PFA, permeabilized using 0.5% Triton and stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG version of 8F5.1A9 (NBP3-12034, blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor(R) 488 antibody at a dilution of 1:1000 and cells were analyzed using a FACSCanto flow-cytometer.")