Human/Mouse RelA/NFkB p65 PE-conjugated Antibody Summary
Asn456-Ser551
Accession # Q04206
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of RelA/NF kappa B p65 in HeLa Human Cell Line by Flow Cytometry. HeLa human cervical epithelial carcinoma cell line was stained with Mouse Anti-Human/Mouse RelA/NF kappa B p65 PE-conjugated Monoclonal Antibody (Catalog # IC5078P, filled histogram) or isotype control antibody (Catalog # IC0041P, open histogram). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005). View our protocol for Staining Intracellular Molecules.
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Preparation and Storage
- 12 months from date of receipt, 2 to 8 °C as supplied.
Background: RelA/NFkB p65
RelA p65 (v-rel reticuloendotheliosis viral oncogene homolog A) is a 65 kDa member of the NF kappa B family of nuclear transcription factors. Dimers of p65 with the p50 subunit are the most common form of the NF kappa B transcription factor, but dimers with it or other family members can also occur. Upon activation, RelA p65 forms an heterotetramer and moves into the nucleus where it binds to specific DNA sequences. An alternatively spliced isoform that lacks amino acids (aa) 222‑231 (p65 delta ) does not bind DNA. Over the sequence used as an immunogen, human RelA p65 shares 96% and 98% aa identity with mouse and rat RelA p65, respectively. This portion includes one of eight potential ser/thr phosphorylation sites, two acetylation sites, and most of the Rel homology domain that interacts with I kappa B inhibitors.
Product Datasheets
Citations for Human/Mouse RelA/NFkB p65 PE-conjugated Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 5
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Autophagy is critical for group 2 innate lymphoid cell metabolic homeostasis and effector function
Authors: Galle-Treger L, Hurrell BP, Lewis G
J Allergy Clin Immunol.
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DR3 stimulation of adipose resident ILC2s ameliorates type 2 diabetes mellitus
Authors: P Shafiei-Ja, BP Hurrell, L Galle-Treg, DG Helou, E Howard, J Painter, R Lo, G Lewis, P Soroosh, O Akbari
Nat Commun, 2020-09-18;11(1):4718.
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CD200-CD200R immune checkpoint engagement regulates ILC2 effector function and ameliorates lung inflammation in asthma
Authors: P Shafiei-Ja, DG Helou, BP Hurrell, E Howard, C Quach, JD Painter, L Galle-Treg, M Li, YE Loh, O Akbari
Nature Communications, 2021-05-05;12(1):2526.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry -
TNFR2 Signaling Enhances ILC2 Survival, Function, and Induction of Airway Hyperreactivity
Authors: BP Hurrell, L Galle-Treg, PS Jahani, E Howard, DG Helou, H Banie, P Soroosh, O Akbari
Cell Rep, 2019-12-24;29(13):4509-4524.e5.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry -
Costimulation of type-2 innate lymphoid cells by GITR promotes effector function and ameliorates type 2 diabetes
Authors: L Galle-Treg, I Sankaranar, BP Hurrell, E Howard, R Lo, H Maazi, G Lewis, H Banie, AL Epstein, P Hu, VK Rehan, FD Gilliland, H Allayee, P Soroosh, AH Sharpe, O Akbari
Nat Commun, 2019-02-12;10(1):713.
Species: Mouse
Sample Types: Whole Cells
Applications: Flow Cytometry
FAQs
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