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anti phosphonf kb  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology anti phosphonf kb
    Anti Phosphonf Kb, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 807 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Incubation:

    Article Title: The Combination of Curcumae Radix and Syzygium Aromaticum Extracts Mitigates Benign Prostatic Hyperplasia through Anti-Proliferative and Anti-Inflammatory Effects.
    Article Snippet: .. The protein samples from the tissue were separated using 4% to 12% SDS-PAGE, transferred onto the PVDF, blocked (5% skim milk), and incubated overnight at 4 °C with specific antibodies such as specific antibodies like anti-NADPH oxidase 4 (NOX4) (#NB110-58851; Novus Biologicals), AR (#19672; Cell Signaling Technologies), PSA/KLK3 (#sc7316; Santa Cruz Biotechnologies), inducible nitric oxide synthase (iNOS) (#sc7271; Santa Cruz Biotechnologies), and cyclooxygenase-2 (COX2) (#sc19999; Santa Cruz Biotechnologies), phospho-extracellular signal-regulated kinases (ERK) (#sc7383; Santa Cruz Biotechnologies), ERK (#sc271269; Santa Cruz Biotechnologies), phosphoNF-kB (#sc271908; Santa Cruz Biotechnologies), NFkB (#sc8414; Santa Cruz Biotechnologies) and β-actin (#sc47778; Santa Cruz Biotechnologies). .. Later, blots were washed, respective species-specific secondary antibodies against mouse or rabbit IgG were added, and signals were detected and visualized with ECL reagent (#1705061; Bio-Rad).



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    Fig. 5 Expression of phosphorylated NFkB <t>p65</t> shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.
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    Fig. 5 Expression of phosphorylated NFkB <t>p65</t> shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.
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    Fig. 5 Expression of phosphorylated NFkB <t>p65</t> shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.
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    Fig. 5 Expression of phosphorylated NFkB <t>p65</t> shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.
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    Fig. 5 Expression of phosphorylated NFkB p65 shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.

    Journal: Food & function

    Article Title: Characterization of different stages of Maillard reaction in soy: impact on physicochemical properties and immunogenicity of soy proteins.

    doi: 10.1039/d4fo04400b

    Figure Lengend Snippet: Fig. 5 Expression of phosphorylated NFkB p65 shows an increased trend in macrophages after stimulation with glycated soy. Expression of phosphorylated NFkB P65, analyzed by western blot (A) THP-1 differen- tiated into macrophages, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy for 10 minutes, data is representative of 3 replicates. (B) Primary derived adherent monocytes from one donor, stimulated with 25 μg ml−1 glycated soy or 100 ng ml−1 LPS and 10 ng ml−1 IFNy, data is representative of two replicates. Quantified data based on the adjusted volume normalized to beta actin. Data was processed and quantified using the ImageLab software from BioRad.

    Article Snippet: The membrane was then washed 3×, followed by incubation with primary antibody (PhosphoNF-κB p65 (Ser536) (93H1) Rabbit mAb, Cell Signaling) overnight at 4 °C.

    Techniques: Expressing, Western Blot, Derivative Assay, Software