A portion of amino acids 545-573 from the human protein were used as the immunogen for the DLL3 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. [provided by RefSeq].
Western blot: 1:500-1:2000,Immunohistochemistry (FFPE): 1:25,Immunofluorescence: 1:25
Anwendungsbeschreibung:
The stated application concentrations are suggested starting points. Titration of the DLL3 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
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