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WuXi AppTec
anti-tlr8 rabbit polyclonal antibody ![]() Anti Tlr8 Rabbit Polyclonal Antibody, supplied by WuXi AppTec, 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/result/anti-tlr8 rabbit polyclonal antibody/product/WuXi AppTec Average 90 stars, based on 1 article reviews
anti-tlr8 rabbit polyclonal antibody - by Bioz Stars,
2026-04
90/100 stars
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Key component of innate and adaptive immunity TLRs Toll like receptors control host immune response against pathogens through recognition of molecular patterns specific of microorganisms Acts via MYD88 and TRAF6 leading to NF kappa B
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This antibody recognizes 120 KDa TLR8 in samples from human mouse and rat origins TLR8 toll like receptor 8 is a protein coding gene Diseases associated with TLR8 include pandas and dengue hemorrhagic fever and
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Key component of innate and adaptive immunity TLRs Toll like receptors control host immune response against pathogens through recognition of molecular patterns specific of microorganisms Acts via MYD88 and TRAF6 leading to NF kappa B
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The protein encoded by this gene is a member of the Toll like receptor TLR family which plays a fundamental role in pathogen recognition and activation of innate immunity TLRs are highly conserved from Drosophila
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Rabbit anti Human TLR8 Polyclonal Antibody
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The protein encoded by this gene is a member of the Toll like receptor TLR family which plays a fundamental role in pathogen recognition and activation of innate immunity TLRs are highly conserved from Drosophila
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Image Search Results
Journal: Respiratory Research
Article Title: Oxidative stress augments toll-like receptor 8 mediated neutrophilic responses in healthy subjects
doi: 10.1186/1465-9921-10-50
Figure Lengend Snippet: Detection of toll-like receptor (TLR) 8 in human polymorphonuclear cells (PMNs), and the effects of TLR 7/8 ligand R848 on interleukin(IL)-8 release . (A) TLR8 in PMN was detected by immunocytochemistry. Left panel indicates isotype control. Right panel shows TLR8 immunoreactivity in PMN. (Original magnification: × 400, Scale bars = 10 μm). (B) TLR8 expression was analyzed by flow-cytometry. PMNs were stained by anti-human TLR8 (solid lines) or the isotype control (gray histograms) in the permeabilized (left panel) and unpermeabilized condition (right panel). Left panel indicates both intercellular and cell surface expression of TLR8. Right panel shows cell surface expression alone. (C-F) Effect of R848 on the release of IL-8, and effect of bafilomycin or dexamethasone on the R848-induced IL-8 release from PMN. (C) PMNs were treated with 10 μM R848. The media were harvested at various time points and assayed for IL-8 by ELISA. (D) PMNs were treated for 24 hrs with R837, a ligand of TLR7, or various concentrations of R848, a ligand of TLR 7/8. Media were assayed for IL-8 by ELISA. (E, F) PMNs were treated with 10 μM R848 or vehicle in the presence of various concentrations of bafilomycin, an inhibitor of endosomal acidification (E), or dexamethasone (F). Media were assayed for IL-8 by ELISA. All values are mean values ± SEM of three to four separate experiments. *p < 0.05, **p < 0.01, compared with the values of control; +p < 0.05, ++p < 0.01, compared with the values of the vehicle-pretreated and 10 μM R848-treated group.
Article Snippet: Commercially available reagents were obtained as follows: Mono-Poly Resolving Medium was from Dainippon Pharmaceutical Co. Ltd. (Osaka, Japan); fetal calf serum (FCS) and RPMI medium 1640 (RPMI 1640) were from Invitrogen (Carlsbad, California, USA); R848 (resiquimod: 4-amino-2-etoxymethyl-α,α-dimethyl-1 H -imidazo [4,5- c ]quinolin-1-ethanol), bafilomycin and 12-o-tetradecanoylphorbol 13-acetate were from Alexis Biochemicals (San Diego, California, USA); R837 (Imiquimod: 1-isobutyl-1 H -imidazo [4,5- c ]quinolin-4-amine) was from Biomol (Plymouth Meeting, Pennsylvania, USA); N-acethyl- L -cysteine, MG-132, dexamethasone and anti-β-actin antibody were from Sigma (St. Louis, Missouri, USA);
Techniques: Immunocytochemistry, Expressing, Flow Cytometry, Staining, Enzyme-linked Immunosorbent Assay