FluoroFinder

	Supplier	US Biological
	Catalog #:	245758-Biotin-100UL (View supplier product page)
	Size	100 μl
	Price	$681.00
	Antigen	EPB41L3
	Clone	1B7
	Host	Mouse
	Isotype	IgG3 κ
	Conjugate	Biotin
	Target Species	Human
	Applications	ELISA, IF, WB
	Description	EPB41L3 (erythrocyte Membrane Protein band 4.1-like 3, 4.1B, DAL-1, DAL1, FLJ37633, KIAA0987) (Biotin) Mab 1B7

	EPB41L3	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]

	Additional Sources

EPB41L3 / Biotin / 1B7