CD40 Antibody - Biotin Conjugated

Cat# OADB00192

Size : 1mL

Brand : Aviva Systems Biology

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Datasheets/ManualsPrintable datasheet for anti-CD40 (OADB00192) antibody
Product Info
Predicted Species ReactivityHuman
Product FormatLyophilized
ClonalityMonoclonal
CloneB-B20
IsotypeMouse IgG1
HostHuman
ConjugationBiotin
ApplicationFC
Reconstitution and StorageReconstitute with 1 mL deionised water
Use 10 uL to label 106 cells or 100 uL of whole blood. Stable at +2-8C for six months after reconstitution. For longer storage, freeze aliquots
PurificationIon exchange chromatography
Concentration100 tests/1mL
PreservativeSodium Azide
SpecificityRecognises the Bp50 antigen, a 48 kDa protein
FormulationLyophilisated in phosphate-buffered saline with 1% BSA and 0.1% sodium azide
Storage BufferLyophilisated in phosphate-buffered saline with 1% BSA and 0.1% sodium azide
ReferenceChalla A. et al, BC12 Leucocyte Typing Workshop VI, Kobe (1996)
Kotowvicz K. et al, BC12.1 Leucocyte Typing Workshop VI, Kobe (1996)
Naito, A. et al., Proc Natl Acad Sci.,2002; 99(13): 8766-71.
Vermot-Desroches C. et al, Immunology Letters 48 : 1-9 (1995)
Gene SymbolCD40
Gene Full NameCD40 molecule
Alias Symbolsp50, Bp50, CDW40, TNFRSF5
NCBI Gene Id958
Protein Nametumor necrosis factor receptor superfamily member 5
Description of TargetThis 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.
Uniprot IDP25942
Protein Accession #NP_001241.1
Nucleotide Accession #NM_001250.5
Molecular Weight31 kDa