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.    

WB    1/500 - 1/2000    

IHC    1/200 - 1/1000    

IF/ICC    1/200 - 1/1000    

FCM    1/200 - 1/400    

ELISA    1/10000