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phospho nf κb ser468  (Bioss)


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    Structured Review

    Bioss phospho nf κb ser468
    Phospho Nf κb Ser468, supplied by Bioss, used in various techniques. Bioz Stars score: 94/100, based on 27 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/phospho nf κb ser468/product/Bioss
    Average 94 stars, based on 27 article reviews
    phospho nf κb ser468 - by Bioz Stars, 2026-02
    94/100 stars

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    The effect of PINO on NF-κB and MAPK pathways. RAW264.7 cells were treated with CPZ (10 μM) or PINO (10 μM) for 1 h, and whole-cell lysates were prepared and immunoblotted using <t>p-p65,</t> p65, p-IκBα, IκBα, p-p38, p38, p-JNK, JNK, p-ERK1/2, ERK1/2, TRPV1, β-actin, GAPDH, and β-tubulin antibody (A) . Fold change was determined after normalization with β-actin, GAPDH, or β-tubulin, with the right panels illustrating the fold change relative to the control: p-p65/p65 (B) , p-IκBα/IκBα (C) , p-p38/p38 (D) , p-JNK/JNK (E) , p-ERK1/2/ERK1/2 (F) and TRPV1/β-actin (G) (n = 6). Data are presented as mean ± SD. Statistical analysis by one-way ANOVA with Bonferroni’s post hoc test.
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    Cell Signaling Technology Inc phosphorylated nf κb p65 p p65
    The effect of PINO on NF-κB and MAPK pathways. RAW264.7 cells were treated with CPZ (10 μM) or PINO (10 μM) for 1 h, and whole-cell lysates were prepared and immunoblotted using <t>p-p65,</t> p65, p-IκBα, IκBα, p-p38, p38, p-JNK, JNK, p-ERK1/2, ERK1/2, TRPV1, β-actin, GAPDH, and β-tubulin antibody (A) . Fold change was determined after normalization with β-actin, GAPDH, or β-tubulin, with the right panels illustrating the fold change relative to the control: p-p65/p65 (B) , p-IκBα/IκBα (C) , p-p38/p38 (D) , p-JNK/JNK (E) , p-ERK1/2/ERK1/2 (F) and TRPV1/β-actin (G) (n = 6). Data are presented as mean ± SD. Statistical analysis by one-way ANOVA with Bonferroni’s post hoc test.
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    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
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    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
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    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
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    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
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    Proteintech phospho nf κb p65 ser468
    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
    Phospho Nf κb P65 Ser468, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Cell Signaling Technology Inc rabbit anti p nf κb
    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) <t>phospho-NF-κB-p65</t> expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.
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    Image Search Results


    The effect of PINO on NF-κB and MAPK pathways. RAW264.7 cells were treated with CPZ (10 μM) or PINO (10 μM) for 1 h, and whole-cell lysates were prepared and immunoblotted using p-p65, p65, p-IκBα, IκBα, p-p38, p38, p-JNK, JNK, p-ERK1/2, ERK1/2, TRPV1, β-actin, GAPDH, and β-tubulin antibody (A) . Fold change was determined after normalization with β-actin, GAPDH, or β-tubulin, with the right panels illustrating the fold change relative to the control: p-p65/p65 (B) , p-IκBα/IκBα (C) , p-p38/p38 (D) , p-JNK/JNK (E) , p-ERK1/2/ERK1/2 (F) and TRPV1/β-actin (G) (n = 6). Data are presented as mean ± SD. Statistical analysis by one-way ANOVA with Bonferroni’s post hoc test.

    Journal: Frontiers in Pharmacology

    Article Title: Identification and evaluation of a pinocembrin analog as a TRPV1 inhibitor with analgesic properties in murine pain models

    doi: 10.3389/fphar.2025.1585181

    Figure Lengend Snippet: The effect of PINO on NF-κB and MAPK pathways. RAW264.7 cells were treated with CPZ (10 μM) or PINO (10 μM) for 1 h, and whole-cell lysates were prepared and immunoblotted using p-p65, p65, p-IκBα, IκBα, p-p38, p38, p-JNK, JNK, p-ERK1/2, ERK1/2, TRPV1, β-actin, GAPDH, and β-tubulin antibody (A) . Fold change was determined after normalization with β-actin, GAPDH, or β-tubulin, with the right panels illustrating the fold change relative to the control: p-p65/p65 (B) , p-IκBα/IκBα (C) , p-p38/p38 (D) , p-JNK/JNK (E) , p-ERK1/2/ERK1/2 (F) and TRPV1/β-actin (G) (n = 6). Data are presented as mean ± SD. Statistical analysis by one-way ANOVA with Bonferroni’s post hoc test.

    Article Snippet: Phospho-NF-κB p65 (Ser468) antibody, NF-κB p65 antibody, Phospho-IκB Alpha (Ser32/36) antibody, IκB Alpha antibody, Phospho-p38 MAPK (Thr180/Tyr182) antibody, p38 MAPK antibody, Phospho-JNK (Tyr185) antibody, JNK antibody, Phospho-ERK1/2 (Thr202/Tyr204) antibody, ERK1/2 antibody, TRPV1 antibody, β-actin antibody, glyceraldehyde 3-phosphate dehydrogenase (GAPDH) antibody, β-Tubulin and Goat Anti-Rabbit IgG (H + L) were purchased from Proteintech Group, Inc. (Wuhan, China).

    Techniques: Control

    Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) phospho-NF-κB-p65 expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.

    Journal: Frontiers in Immunology

    Article Title: Extracellular microvesicles from patients with Rheumatoid arthritis promote dendritic cell activation in vitro

    doi: 10.3389/fimmu.2025.1532114

    Figure Lengend Snippet: Analysis of MAPK and NF-κB activation in DCs stimulated with RA patient EMVs. DCs untreated or stimulated with LPS, RA patient EMVs and HD EMVs were lysed and analyzed by western blot to evaluate: (A) Phospho-p38 expression using rabbit anti-phospho-p38 Ab. (B) Phospho-ERK expression using rabbit anti-phospho-ERK1/2 Ab. (C) phospho-NF-κB-p65 expression using rabbit anti-phospho-NF-κB-p65 Ab. Anti-β-tubulin mAb or anti-β-actin mAb were used to evaluate loading controls. Samples from one representative RA patient and HD are shown. Densitometric phospho-proteins/total proteins ratios were calculated in all HDs and RA patients and are summarized by histograms in the right panels of the figure. Data are reported as mean (S.D.). Statistical analysis indicated: **p < 0.01; ***p < 0.001; ****p < 0.0001.

    Article Snippet: The PVDF membranes containing the samples stimulated for 15 min were incubated with polyclonal rabbit anti-phospho-ERK1/2 or anti-phospho-p38 Abs (Cell Signaling, Inc. Danvers, MA, USA); alternatively, the PVDF membranes containing samples stimulated for 45 min were incubated with polyclonal rabbit anti-phospho NF-κB-p65 (Cell Signaling, Inc.).

    Techniques: Activation Assay, Western Blot, Expressing