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antinfκb antibody  (Proteintech)


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    Structured Review

    Proteintech antinfκb antibody
    Antinfκb Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1726 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/antinf%CE%BAb+antibody/Histone-H3+Antibody/pm37903782-209-6-9
    Average 96 stars, based on 1726 article reviews
    antinfκb antibody - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Immunoprecipitation:

    Article Title: IDO1 facilitates esophageal carcinoma progression by driving the direct binding of NF-κB and CXCL10.
    Article Snippet: .. The clipped chromatin was immunoprecipitated with antiNFκB antibody (1:100, Proteintech, Wuhan, China), Histone H3 (D2B12) XP® Rabbit mAb (2 μg, Cell Signaling Technology, Danvers, Massachusetts, USA) or Normal Rabbit IgG (2 μg, Cell Signaling Technology) overnight at 4 °C. ..



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    Santa Cruz Biotechnology antibodies antinfκb p65
    Figure 4. NF-κB activation by PT-gliadin. Caco-2 monolayers were challenged with PT-gliadin (1 mg/mL) or with preincubated solutions of PT-gliadin and anti-PT-gliadin IgY (3.5 mg/mL), or were left untreated for 45 min. (A) Whole cell lysates were subjected to Western blot analysis for phosphorylated NF- κB <t>p65,</t> total NF-κB p65, and GAPDH (as a loading control). Changes of (B) phosphorylated NF-κB p65 and total NF-κB p65 levels upon addition of anti-PT-gliadin IgY (specific IgY) were calculated by normalizing data to the PT-gliadin-treated sample (= 1). Data are depicted as means ± SEM; *indicates a significant difference with p < 0.05.
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    Figure 4. NF-κB activation by PT-gliadin. Caco-2 monolayers were challenged with PT-gliadin (1 mg/mL) or with preincubated solutions of PT-gliadin and anti-PT-gliadin IgY (3.5 mg/mL), or were left untreated for 45 min. (A) Whole cell lysates were subjected to Western blot analysis for phosphorylated NF- κB <t>p65,</t> total NF-κB p65, and GAPDH (as a loading control). Changes of (B) phosphorylated NF-κB p65 and total NF-κB p65 levels upon addition of anti-PT-gliadin IgY (specific IgY) were calculated by normalizing data to the PT-gliadin-treated sample (= 1). Data are depicted as means ± SEM; *indicates a significant difference with p < 0.05.
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    Santa Cruz Biotechnology antinfκb p65 c 20 antibody
    Figure 4. NF-κB activation by PT-gliadin. Caco-2 monolayers were challenged with PT-gliadin (1 mg/mL) or with preincubated solutions of PT-gliadin and anti-PT-gliadin IgY (3.5 mg/mL), or were left untreated for 45 min. (A) Whole cell lysates were subjected to Western blot analysis for phosphorylated NF- κB <t>p65,</t> total NF-κB p65, and GAPDH (as a loading control). Changes of (B) phosphorylated NF-κB p65 and total NF-κB p65 levels upon addition of anti-PT-gliadin IgY (specific IgY) were calculated by normalizing data to the PT-gliadin-treated sample (= 1). Data are depicted as means ± SEM; *indicates a significant difference with p < 0.05.
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    Image Search Results


    Figure 4. NF-κB activation by PT-gliadin. Caco-2 monolayers were challenged with PT-gliadin (1 mg/mL) or with preincubated solutions of PT-gliadin and anti-PT-gliadin IgY (3.5 mg/mL), or were left untreated for 45 min. (A) Whole cell lysates were subjected to Western blot analysis for phosphorylated NF- κB p65, total NF-κB p65, and GAPDH (as a loading control). Changes of (B) phosphorylated NF-κB p65 and total NF-κB p65 levels upon addition of anti-PT-gliadin IgY (specific IgY) were calculated by normalizing data to the PT-gliadin-treated sample (= 1). Data are depicted as means ± SEM; *indicates a significant difference with p < 0.05.

    Journal: SLAS discovery : advancing life sciences R & D

    Article Title: A Screening Approach for Identifying Gliadin Neutralizing Antibodies on Epithelial Intestinal Caco-2 Cells.

    doi: 10.1177/2472555217697435

    Figure Lengend Snippet: Figure 4. NF-κB activation by PT-gliadin. Caco-2 monolayers were challenged with PT-gliadin (1 mg/mL) or with preincubated solutions of PT-gliadin and anti-PT-gliadin IgY (3.5 mg/mL), or were left untreated for 45 min. (A) Whole cell lysates were subjected to Western blot analysis for phosphorylated NF- κB p65, total NF-κB p65, and GAPDH (as a loading control). Changes of (B) phosphorylated NF-κB p65 and total NF-κB p65 levels upon addition of anti-PT-gliadin IgY (specific IgY) were calculated by normalizing data to the PT-gliadin-treated sample (= 1). Data are depicted as means ± SEM; *indicates a significant difference with p < 0.05.

    Article Snippet: The gels were blotted to nitrocellulose membranes (TransBlot Turbo Mini Nitrocellulose Transfer Packs, Bio-Rad), and the membranes blocked afterward with 5% BSA in TBS-T (50 mM Tris [pH 7.5], 150 mM NaCl, and 0.1% Tween-20) and probed with the primary antibodies antiNFκB p65 (sc-8008, Santa Cruz), anti-phospho-NFκB p65 (Ser536; 3033S, CST), and anti-GAPDH (2118S, CST) as control.

    Techniques: Activation Assay, Western Blot, Control