RM2120

DLL3 (16H17) Rabbit Monoclonal Antibody

SCDO1

常规抗体

WB

Human,Mouse

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% New type preservative N and 0.05% BSA.

A synthetic peptide of human DLL3

WB: 1:1000 IHC: 1:100 ICC/IF: 1:100 FC: 1:200-1:500 IP: 1:20

65kDa

65kDa

-20°C/1 year

Rabbit

IgG

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, Jul 2008]

Affinity Purification