p-p65 rabbit ab antibody  (Cell Signaling Technology Inc)

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

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

Journal: Frontiers in Pharmacology

Article Title: Ningmitai capsules have anti-inflammatory and pain-relieving effects in the chronic prostatitis/chronic pelvic pain syndrome mouse model through systemic immunity

doi: 10.3389/fphar.2022.949316

Figure Lengend Snippet: Antibody information used in the article.

Article Snippet: p-P65 Rabbit Ab , 1:1,000(WB) , CST (3,031).

Techniques:

Journal: Frontiers in Pharmacology

Article Title: Ningmitai capsules have anti-inflammatory and pain-relieving effects in the chronic prostatitis/chronic pelvic pain syndrome mouse model through systemic immunity

doi: 10.3389/fphar.2022.949316

Figure Lengend Snippet: Decreased prostatic inflammation and inflammatory pain-related pathway activation in mice. (A) Sections of prostate tissues were stained with HE. Scale bar = 50 μm; CTL = control; EAP = experimental autoimmune prostatitis mice; NMT: Ningmitai-treated mice. (B) Inflammatory scores of the CTL, EAP, and NMT groups. n = 6. (C) Thirteen inflammatory-related factors in the CTL, EAP, and NMT groups. n = 6. (D) Western blotting analyzing of p-JNK, JNK, p-ERK, ERK, p-P38, P38, p-P65, P65, p-STAT3, STAT3, and GAPDH expressions as well as a statistical analysis of the results in the CTL, EAP, and NMT groups. n = 6. (*: p < 0.05; **: p < 0.01)

Article Snippet: p-P65 Rabbit Ab , 1:1,000(WB) , CST (3,031).

Techniques: Activation Assay, Staining, Control, Western Blot

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