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p p65 ser536  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc p p65 ser536
    P P65 Ser536, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1893 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti-p-p65+ab/Anti-rabbit+IgG+(H%2BL)%2C+F(ab')+2+Fragment/pmc09413377-35-3-14
    Average 98 stars, based on 1893 article reviews
    p p65 ser536 - by Bioz Stars, 2026-10
    98/100 stars

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    Figure 2. Patients with NOD2 E383D have decreased NF-kB activation and increased levels of P-ERK. Equal numbers of freshly isolated PBMCs from healthy donors (C1–C3), patients with BS (P1–P3) and treatment controls (T1 and T2) were lysed and loaded onto SDS-PAGE. This was followed by Western blot for activation markers of NF-kB and MAP kinase. Levels of <t>P-p65</t> and P-IkBa are decreased in patient samples and treatment controls vs. healthy controls. Levels of P-p38 were similar between patients and controls. Total GAPDH levels act as a loading control. The figure represents a single Western blot experiment.
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    FIGURE 5 | Activation of p38, p44/42 MAPK and <t>NF-kB</t> <t>p65</t> in DC infected with wild type USA300 or esx mutants. The activation of intracellular pathway involving p38, p42/44 MAPK, and NF-kB <t>p65</t> <t>subunit</t> was investigated by western blotting analysis of the phosphorylated isoforms in whole cell extracts prepared from DC infected for 1 (A) and 3 h (B) with wild type USA300 or esx mutants. β-actin levels were analyzed as control for protein loading. Fold changes of each analyzed protein, indicated at the bottom of each immunoblot, were calculated by dividing values obtained in infected conditions with those of the uninfected counterpart. A representative experiment, out of 3 independent experiments performed that yielded similar results, is shown.
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    Image Search Results


    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Article Snippet: p-p65 Rabbit Ab , Bioss , bs-0982R , 1: 1500.

    Techniques: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Article Snippet: p-p65 Rabbit Ab , Bioss , bs-0982R , 1: 1500.

    Techniques: Activity Assay

    Figure 2. Patients with NOD2 E383D have decreased NF-kB activation and increased levels of P-ERK. Equal numbers of freshly isolated PBMCs from healthy donors (C1–C3), patients with BS (P1–P3) and treatment controls (T1 and T2) were lysed and loaded onto SDS-PAGE. This was followed by Western blot for activation markers of NF-kB and MAP kinase. Levels of P-p65 and P-IkBa are decreased in patient samples and treatment controls vs. healthy controls. Levels of P-p38 were similar between patients and controls. Total GAPDH levels act as a loading control. The figure represents a single Western blot experiment.

    Journal: Innate immunity

    Article Title: A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.

    doi: 10.1177/1753425917727063

    Figure Lengend Snippet: Figure 2. Patients with NOD2 E383D have decreased NF-kB activation and increased levels of P-ERK. Equal numbers of freshly isolated PBMCs from healthy donors (C1–C3), patients with BS (P1–P3) and treatment controls (T1 and T2) were lysed and loaded onto SDS-PAGE. This was followed by Western blot for activation markers of NF-kB and MAP kinase. Levels of P-p65 and P-IkBa are decreased in patient samples and treatment controls vs. healthy controls. Levels of P-p38 were similar between patients and controls. Total GAPDH levels act as a loading control. The figure represents a single Western blot experiment.

    Article Snippet: Abs against P-p65 (#3033), IkBa (#9242), P-IkBa (#9246), P-ERK (#9101) and P-p38 (#4511) were purchased from Cell Signaling Technology (Danvers, MA, USA).

    Techniques: Activation Assay, Isolation, SDS Page, Western Blot, Control

    FIGURE 5 | Activation of p38, p44/42 MAPK and NF-kB p65 in DC infected with wild type USA300 or esx mutants. The activation of intracellular pathway involving p38, p42/44 MAPK, and NF-kB p65 subunit was investigated by western blotting analysis of the phosphorylated isoforms in whole cell extracts prepared from DC infected for 1 (A) and 3 h (B) with wild type USA300 or esx mutants. β-actin levels were analyzed as control for protein loading. Fold changes of each analyzed protein, indicated at the bottom of each immunoblot, were calculated by dividing values obtained in infected conditions with those of the uninfected counterpart. A representative experiment, out of 3 independent experiments performed that yielded similar results, is shown.

    Journal: Frontiers in cellular and infection microbiology

    Article Title: Staphylococcus aureus Esx Factors Control Human Dendritic Cell Functions Conditioning Th1/Th17 Response.

    doi: 10.3389/fcimb.2017.00330

    Figure Lengend Snippet: FIGURE 5 | Activation of p38, p44/42 MAPK and NF-kB p65 in DC infected with wild type USA300 or esx mutants. The activation of intracellular pathway involving p38, p42/44 MAPK, and NF-kB p65 subunit was investigated by western blotting analysis of the phosphorylated isoforms in whole cell extracts prepared from DC infected for 1 (A) and 3 h (B) with wild type USA300 or esx mutants. β-actin levels were analyzed as control for protein loading. Fold changes of each analyzed protein, indicated at the bottom of each immunoblot, were calculated by dividing values obtained in infected conditions with those of the uninfected counterpart. A representative experiment, out of 3 independent experiments performed that yielded similar results, is shown.

    Article Snippet: Blots were incubated with rabbit polyclonal antiphospho-p38 MAPK (Thr180/Tyr182) (p-p38), rabbit polyclonal anti-phospho-p44/42 MAPK (Thr202/Tyr204) (p-p44/42) and rabbit polyclonal anti-phospho-NF-kB p65 (Ser536) (p-p65) Abs (Cell Signaling Technology, Danvers, MA).

    Techniques: Activation Assay, Infection, Western Blot, Control