DLL3 is 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.
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.
Applications:Suitable for use in Western Blot.
Other applications not tested.
Recommended Dilutions:Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：100ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by affinity chromatography.
Form：Supplied as a liquid in PBS, 0.09% sodium azide, 2% sucrose
Specificity：Recognizes human DLL3
Isotype：IgG
Calc Applications Abbrev：WB
Calc Crossreactivity：Hu
Immunogen：Synthetic peptide located within the following region: MVSPRMSGLLSQTVILALIFLPQTRPAGVFELQIHSFGPGPGPGAPRSPCcorresponding to the N-terminal region of human DLL3. Species sequence homology: bovine, canine, guinea pig, mouse, porcine, rabbit, rat
