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monoclonal mouse anti ikkβ 10ag2  (Novus Biologicals)


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    Novus Biologicals monoclonal mouse anti ikkβ 10ag2
    Monoclonal Mouse Anti Ikkβ 10ag2, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+ikk%CE%B2/IKK+beta+Antibody+(10AG2)+-+BSA+Free/pmc12208667-261-0-10
    Average 92 stars, based on 17 article reviews
    monoclonal mouse anti ikkβ 10ag2 - by Bioz Stars, 2026-09
    92/100 stars

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    Article Title: T Cell Receptor Signals to NF-κB Are Transmitted by a Cytosolic p62-Bcl10-Malt1-IKK Signalosome
    Article Snippet: Primary antibodies used in this study were as follows: rabbit anti-Carma1 (Enzo, ALX-210-903), mouse anti-Bcl10 (Santa Cruz Biotechnology, sc-5273), rabbit anti-p62 (Sigma, P0067), mouse anti-tubulin (Santa Cruz Biotechnology, sc-5286), rabbit anti-PKCθ (Cell Signaling Technology), mouse anti-PKCθ (Enzo), anti-pERK1/2 (Cell Signaling Technology, 4370), mouse anti-GAPDH (Santa Cruz Biotechnology, sc-32233), mouse anti-tubulin (Santa Cruz Biotechnology, sc-5286), rabbit anti-pIKKα/β (Cell Signaling Technology, 2694), mouse anti-IKKβ (Imgenex, clone 10A9B6 (used in ) and clone 10AG2 (used in fig. S1B ), mouse anti-TRAF6 (Santa Cruz Biotechnology, sc-8409), mouse anti-pIκBα (Cell Signaling Technology, 9246), and rabbit anti-RelA (Santa Cruz Biotechnology, sc-372).

    Article Title: T Cell Receptor Signals to NF-κB Are Transmitted by a Cytosolic p62-Bcl10-Malt1-IKK Signalosome
    Article Snippet: Antibodies Primary antibodies used in this study were as follows: rabbit anti-Carma1 (Enzo, ALX-210-903), mouse anti-Bcl10 (Santa Cruz Biotechnology, sc-5273), rabbit anti-p62 (Sigma, P0067), mouse anti-tubulin (Santa Cruz Biotechnology, sc-5286), rabbit anti-PKCθ (Cell Signaling Technology), mouse anti-PKCθ (Enzo), anti-pERK1/2 (Cell Signaling Technology, 4370), mouse anti-GAPDH (Santa Cruz Biotechnology, sc-32233), mouse anti-tubulin (Santa Cruz Biotechnology, sc-5286), rabbit anti-pIKKα/β (Cell Signaling Technology, 2694), mouse anti-IKKβ (Imgenex, clone 10A9B6 (used in ) and clone 10AG2 (used in fig. S1B ), mouse anti-TRAF6 (Santa Cruz Biotechnology, sc-8409), mouse anti-pIκBα (Cell Signaling Technology, 9246), and rabbit anti-RelA (Santa Cruz Biotechnology, sc-372).



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    Overexpression of FOSL1 in GBM positively influences NF-κB. ( A-D ) A172, U87MG, and PDX-L14 cells were transfected with GFP-tagged human FOSL1 (FOSL1) and controls (Ctrl) followed by assaying protein expression of FOSL1 and GFP by Western blot ( A ), mRNA expression of FOS1 by qPCR ( B ), GFP positive cell by flow cytometry ( C ), and by immunofluorescence staining ( D : A172-left, U87MG-middle, and PDX-L14-right). ( E ) The identical cellular samples, treated as detailed in ( A-D ), were subjected to ELISA analysis to quantify the relative NF-κB activity in nuclear fraction lysates (* denotes significance at p < 0.05 compared to control using a Student’s t-test). ( F ) Subsequent to the procedures outlined in ( E ), qPCR was conducted to evaluate the mRNA levels of NF-κB p65 and p50. ( G ) Following the protocols described in ( E ), Western blotting was employed to examine the levels of FOSL1 protein, along with phosphorylated (p-IKKβ) and total IKKβ, phosphorylated (p-IKBα) and total IKBα, and phosphorylated (p-P65) and total NF-κB p65. Densitometry analysis for Western blots was performed using the Image Quant program, with the corresponding results positioned below or adjacent to each image. The bar graphs represent the mean ± S.D. of three independent experiments

    Journal: Cellular and Molecular Life Sciences: CMLS

    Article Title: Interaction of NF-κB and FOSL1 drives glioma stemness

    doi: 10.1007/s00018-024-05293-1

    Figure Lengend Snippet: Overexpression of FOSL1 in GBM positively influences NF-κB. ( A-D ) A172, U87MG, and PDX-L14 cells were transfected with GFP-tagged human FOSL1 (FOSL1) and controls (Ctrl) followed by assaying protein expression of FOSL1 and GFP by Western blot ( A ), mRNA expression of FOS1 by qPCR ( B ), GFP positive cell by flow cytometry ( C ), and by immunofluorescence staining ( D : A172-left, U87MG-middle, and PDX-L14-right). ( E ) The identical cellular samples, treated as detailed in ( A-D ), were subjected to ELISA analysis to quantify the relative NF-κB activity in nuclear fraction lysates (* denotes significance at p < 0.05 compared to control using a Student’s t-test). ( F ) Subsequent to the procedures outlined in ( E ), qPCR was conducted to evaluate the mRNA levels of NF-κB p65 and p50. ( G ) Following the protocols described in ( E ), Western blotting was employed to examine the levels of FOSL1 protein, along with phosphorylated (p-IKKβ) and total IKKβ, phosphorylated (p-IKBα) and total IKBα, and phosphorylated (p-P65) and total NF-κB p65. Densitometry analysis for Western blots was performed using the Image Quant program, with the corresponding results positioned below or adjacent to each image. The bar graphs represent the mean ± S.D. of three independent experiments

    Article Snippet: Mouse monoclonal anti-FOSL1 antibody (cat. no. sc-283,107, for Western blotting), mouse monoclonal anti-NF-κB p65 antibody (cat. no. sc-8008), mouse monoclonal anti-p53 antibody (cat. no. sc-7974), mouse monoclonal anti-PTEN antibody (cat. no. sc-126), and mouse IKKβ monoclonal antibody (cat. no. sc-8014) were purchased from Santa Cruz Biotechnology.

    Techniques: Over Expression, Transfection, Expressing, Western Blot, Flow Cytometry, Immunofluorescence, Staining, Enzyme-linked Immunosorbent Assay, Activity Assay, Control