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 IgG1
Species Reactivity： Human
Immunogen： Purified recombinant fragment of human DLL3 (AA: extra 27-226) expressed in E. Coli.
