catalog number :
MBS859657
products full name :
B-cell surface antigen CD40, Bp50, CD40 antigen, CD40 receptor, CDw40, TNR5; tumor necrosis factor receptor superfamily member 5, TNFRSF5
products short name :
CD40
other names :
CD40, partial; CD40; CD40
products gene name :
CD40
uniprot entry name :
Q09LL4_HUMAN
reactivity :
Human, Mouse
specificity :
CD40 antibody detects endogenous levels of total CD40 protein.
purity :
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
form :
Rabbit IgG in phosphate buffered saline (without Mg 2+ and Ca 2+ ), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
storage stability :
Store at -20 degree C/1 year
tested application :
Western Blot (WB), Immunohistochemistry (IHC)
app notes :
WB: 1:500-1:1000 . IHC: 1:50-1:100. ELISA: 1 :10000
other info1 :
Swiss-Prot No.: P25942. Immunogen: The antiserum was produced against synthesized peptide derived from C-terminal of human CD40.
products categories :
Cancer; Cardiovascular; Cell Biology; Epigenetics & Nuclear Signaling; Developmental Biologys; Immunology; Drug Discovery Products; Metabolism; Neuroscience; Signal Transduction; Stem Cells; Autophagy antibody
ncbi acc num :
ABI49511.1
ncbi mol weight :
13,158 Da
ncbi summary :
This 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]