The antiserum was produced against synthesized peptide derived from human TNFRSF5 around the phosphorylation site of Thr254. AA range:220-269

Phospho-CD40 (T254) Polyclonal Antibody detects endogenous levels of CD40 protein only when phosphorylated at T254.The name of modified sites may be influenced by many factors, such as species (the modified site was not originally found in human samples) and the change of protein sequence (the previous protein sequence is incomplete, and the protein sequence may be prolonged with the development of protein sequencing technology). When naming, we will use the "numbers" in historical reference to keep the sites consistent with the reports. The antibody binds to the following modification sequence (lowercase letters are modification sites):QEtLH

CD40

Tumor necrosis factor receptor superfamily member 5

CD40 ;
TNFRSF5 ;
Tumor necrosis factor receptor superfamily member 5 ;
B-cell surface antigen CD40 ;
Bp50 ;
CD40L receptor ;
CDw40 ;
CD antigen CD40

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 (HIG

Alternative products:Additional isoforms seem to exist,Disease:Defects in CD40 are the cause of hyper-IgM immunodeficiency type 3 (HIGM3) [MIM:606843]. HIGM3 is an autosomal recessive disorder which includes an inability of B cells to undergo isotype switching, one of the final differentiation steps in the humoral immune system, an inability to mount an antibody-specific immune response, and a lack of germinal center formation.,Function:Receptor for TNFSF5/CD40LG.,online information:CD40 entry,online information:CD40 mutation db,similarity:Contains 4 TNFR-Cys repeats.,subunit:Monomer and homodimer. The variant form found in the bladder carcinoma cell line Hu549 does not form homodimers. Interacts with TRAF1, TRAF2, TRAF3, TRAF5 and TRAF6.,tissue specificity:B-cells and in primary carcinomas.,

[Isoform I]: Cell membrane; Single-pass type I membrane protein.; [Isoform II]: Secreted.

>>Cytokine-cytokine receptor interaction ;
>>NF-kappa B signaling pathway ;
>>Cell adhesion molecules ;
>>Toll-like receptor signaling pathway ;
>>Intestinal immune network for IgA production ;
>>Malaria ;
>>Toxoplasmosis ;
>>Human T-cell leukemia virus 1 infection ;
>>Epstein-Barr virus infection ;
>>Transcriptional misregulation in cancer ;
>>Asthma ;
>>Autoimmune thyroid disease ;
>>Systemic lupus erythematosus ;
>>Allograft rejection ;
>>Primary immunodeficiency ;
>>Viral myocarditis ;
>>Lipid and atherosclerosis