该DLL3 Polyclonal Antibody. 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.
应用类型
WB
免疫原
KLH conjugated Synthetic peptide corresponding to Mouse DLL3
