This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene.
Aliases： SCDO1
Entrez GeneID： 10683
Swissprot： Q9NYJ7
WB Predicted band size ： 65KDa
Host/Isotype ： Mouse IgG2a
Species Reactivity ： Human, Rat
Immunogen ： Purified recombinant fragment of human DLL3 (AA: EXTRA(27-226)) expressed in E. Coli.
