Technical Data
034667
DLL3, CT (DLL3, Delta-like protein 3, Drosophila Delta homolog 3)
Description:
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].

Applications:
Suitable for use in Western Blot, Immunohistochemistry, Immunofluorescence, ELISA

Recommended Dilution:
ELISA: 1:1,000
Western Blot: 1:100-500
Immunohistochemistry: 1:10-50
Immunofluorescence: 1:10-50

Storage and Stability:
May be stored at 4C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
TypeIsotypeCloneGrade
PabIgGAffinity Purified
SizeStorageShippingSourceHost
200ul-20CBlue IceHumanRabbit
Concentration:
As reported
Immunogen:
DLL3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 552-583 amino acids from the C-terminal region of human DLL3.
Purity:
Purified by Protein A affinity chromatography.
Form
Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.
Specificity:
Human
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.
Yerges, L.M., et al. J. Bone Miner. Res. 24(12):2039-2049(2009)
Heuss, S.F., et al. Proc. Natl. Acad. Sci. U.S.A. 105(32):11212-11217(2008)
Maisenbacher, M.K., et al. Hum. Genet. 116(5):416-419(2005)
Whittock, N.V., et al. Clin. Genet. 66(1):67-72(2004)
Bonafe, L., et al. Clin. Genet. 64(1):28-35(2003)