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rabbit mab phosphonf κb p65 ser536 93h1 rabbit mab  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit mab phosphonf κb p65 ser536 93h1 rabbit mab
    Rabbit Mab Phosphonf κb P65 Ser536 93h1 Rabbit Mab, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 7464 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 7464 article reviews
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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. 4. Combination treatment with PTX and RSL3 activates NF-κB and promotes TNBC cell death. (A) The viability of MDA-MB-231 and MDA-MB-468 cells was assayed using the CCK-8 assay after combination treatment with PTX or RSL3 and an NF-κB inhibitor for 24 h. (B) After the treatments, the expression levels of cytokines were detected by RT-qPCR. (C) After the treatments, the expression levels of cytokines were detected by Western blotting and ELISA. (D) The protein expression levels of <t>P65,</t> P-P65 and GPX4 were measured by Western blotting, and a grayscale map of protein expression is displayed. **P < 0.01; *P < 0.05; ****p < 0.0001; ***p < 0.001. NS: Not significant.
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    Fig. 4. Combination treatment with PTX and RSL3 activates NF-κB and promotes TNBC cell death. (A) The viability of MDA-MB-231 and MDA-MB-468 cells was assayed using the CCK-8 assay after combination treatment with PTX or RSL3 and an NF-κB inhibitor for 24 h. (B) After the treatments, the expression levels of cytokines were detected by RT-qPCR. (C) After the treatments, the expression levels of cytokines were detected by Western blotting and ELISA. (D) The protein expression levels of <t>P65,</t> P-P65 and GPX4 were measured by Western blotting, and a grayscale map of protein expression is displayed. **P < 0.01; *P < 0.05; ****p < 0.0001; ***p < 0.001. NS: Not significant.
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    Image Search Results


    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

    Fig. 4. Combination treatment with PTX and RSL3 activates NF-κB and promotes TNBC cell death. (A) The viability of MDA-MB-231 and MDA-MB-468 cells was assayed using the CCK-8 assay after combination treatment with PTX or RSL3 and an NF-κB inhibitor for 24 h. (B) After the treatments, the expression levels of cytokines were detected by RT-qPCR. (C) After the treatments, the expression levels of cytokines were detected by Western blotting and ELISA. (D) The protein expression levels of P65, P-P65 and GPX4 were measured by Western blotting, and a grayscale map of protein expression is displayed. **P < 0.01; *P < 0.05; ****p < 0.0001; ***p < 0.001. NS: Not significant.

    Journal: Scientific reports

    Article Title: RSL3 induces ferroptosis by activating the NF-κB signalling pathway to enhance the chemosensitivity of triple-negative breast cancer cells to paclitaxel.

    doi: 10.1038/s41598-025-85774-w

    Figure Lengend Snippet: Fig. 4. Combination treatment with PTX and RSL3 activates NF-κB and promotes TNBC cell death. (A) The viability of MDA-MB-231 and MDA-MB-468 cells was assayed using the CCK-8 assay after combination treatment with PTX or RSL3 and an NF-κB inhibitor for 24 h. (B) After the treatments, the expression levels of cytokines were detected by RT-qPCR. (C) After the treatments, the expression levels of cytokines were detected by Western blotting and ELISA. (D) The protein expression levels of P65, P-P65 and GPX4 were measured by Western blotting, and a grayscale map of protein expression is displayed. **P < 0.01; *P < 0.05; ****p < 0.0001; ***p < 0.001. NS: Not significant.

    Article Snippet: NF-κB p65 (D14E12) rabbit monoclonal antibody (8242), phosphoNF-κB p65 (Ser536) rabbit monoclonal antibody (3033), and anti-rabbit IgG (H + L) (DyLightTM 800 4X PEG Conjugate) rabbit secondary antibody (5151) were purchased from Cell Signaling Technology (CST).

    Techniques: CCK-8 Assay, Expressing, Quantitative RT-PCR, Western Blot, Enzyme-linked Immunosorbent Assay