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WASP/Wiskott-Aldrich syndrome protein Rabbit pAb

Cat No.: APA1670
Size:
Product Name: WASP/Wiskott-Aldrich syndrome protein Rabbit pAb
Cat No.: APA1670
source: Rabbit
reactivity: Human
applications: WB,IHC,ICC/IF,FC
clonality: Polyclonal
recommended dilution: WB: 1:2000-1:10000
IHC: 1:50
ICC/IF: 1:50
FC: 1:20
format: Liquid
isotype: IgG
immunogen: A synthetic peptide of human WASP/Wiskott-Aldrich syndrome protein
calculated molecular weight: 53 kDa
observed molecular weight: 60 kDa
genbank accession number: P42768
gene id (ncbi): 7454
purification method: Affinity Purification
conjugate: Un-conjugated
storage: Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
synonyms: THC; IMD2; SCNX; THC1; WASP; WASPA
category: Primary Ab
concentration: 0.5mg/ml
background: The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5-- UTR sequence, has been described, however, its full-length nature is not known. [provided by RefSeq, Jul 2008]