RelA/NFkB p65 [p Ser536] Antibody

Western Blot: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] -

Western Blot: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] - Western Blot analysis of various cells using NB100-82088 diluted at 1:2000

Immunocytochemistry/ Immunofluorescence: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] -

Immunocytochemistry/ Immunofluorescence: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] - Immunofluorescence staining of methanol-fixed Hela cells using NB100-82088.

Immunohistochemistry-Paraffin: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] -

Immunohistochemistry-Paraffin: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] - Analysis of paraffin-embedded human breast carcinoma tissue using NB100-82088 incubated with blocking peptide (right)

Western Blot: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] -

Effects of RHSL on the translocation of phosphorylated NF-kappa B into the nucleus in TLR-7 agonist-stimulated RAW264.7 cells. Cells were treated with a concentration of 10 μg/mL TLR-7 agonist or 100 μg/mL RHSL, either alone or in combination, for 24 h. Nuclear-cytoplasmic fractionation analysis was performed to quantify the levels of phosphorylated NF-kappa B and total NF-kappa B in cytoplasmic (A) and nuclear (B) protein extracts, respectively. GAPDH and Lamin A/C were used as internal controls for cytoplasmic and nuclear fractions, respectively. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39337618), licensed under a CC-BY license. Not internally tested by Novus Biologicals.

Western Blot: RelA/NFkB p65 [p Ser536] Antibody [NB100-82088] -

Effects of RHSL on the translocation of phosphorylated NF-kappa B into the nucleus in TLR-7 agonist-stimulated RAW264.7 cells. Cells were treated with a concentration of 10 μg/mL TLR-7 agonist or 100 μg/mL RHSL, either alone or in combination, for 24 h. Nuclear-cytoplasmic fractionation analysis was performed to quantify the levels of phosphorylated NF-kappa B and total NF-kappa B in cytoplasmic (A) and nuclear (B) protein extracts, respectively. GAPDH and Lamin A/C were used as internal controls for cytoplasmic and nuclear fractions, respectively. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39337618), licensed under a CC-BY license. Not internally tested by Novus Biologicals.