![Flow Cytometry: Mouse splenocytes stained with ARG22902 anti-CD40 antibody [3/23] (low endotoxin). Flow Cytometry: Mouse splenocytes stained with ARG22902 anti-CD40 antibody [3/23] (low endotoxin).](https://www.arigobio.com/files/product/14593/ARG22902_FACS_1.jpg)
Flow Cytometry: Mouse splenocytes stained with ARG22902 anti-CD40 antibody [3/23] (low endotoxin).
anti-CD40 antibody [3/23] (low endotoxin)

ARG22902
ApplicationsFunctional Assay, Flow Cytometry, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen
Product group Antibodies
ReactivityMouse
TargetCd40
Overview
- SupplierArigo Biolaboratories
- Product Nameanti-CD40 antibody [3/23] (low endotoxin)
- Delivery Days Customer23
- ApplicationsFunctional Assay, Flow Cytometry, ELISA, ImmunoHistoChemistry, ImmunoHistoChemistry Frozen
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone ID3/23
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID21939
- Target nameCd40
- Target descriptionCD40 antigen
- Target synonymsAI326936; B-cell surface antigen CD40; Bp5; Bp50; CD40L receptor; GP39; HIGM1; IGM; IMD3; p5; p50; T-BAM; T-cell differentiation antigen; Tnfr; Tnfrsf5; TRAP; tumor necrosis factor receptor superfamily member 5
- HostRat
- IsotypeIgG2a
- Scientific DescriptionThis gene is a member of the TNF-receptor superfamily. The encoded protein is a receptor on antigen-presenting cells of the immune system and is essential for mediating a broad variety of immune and inflammatory responses including T cell-dependent immunoglobulin class switching, memory B cell development, and germinal center formation. AT-hook transcription factor AKNA is reported to coordinately regulate the expression of this receptor and its ligand, which may be important for homotypic cell interactions. Adaptor protein TNFR2 interacts with this receptor and serves as a mediator of the signal transduction. The interaction of this receptor and its ligand is found to be necessary for amyloid-beta-induced microglial activation, and thus is thought to be an early event in Alzheimer disease pathogenesis. Mutations affecting this gene are the cause of autosomal recessive hyper-IgM immunodeficiency type 3 (HIGM3). Multiple alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Nov 2014]
- ReactivityMouse
- Storage Instruction-20°C
- UNSPSC12352203