DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing The predominant isoform

The predominant isoform

this kit offers endless possibilities for analyzing and studying glycan structures

heparin sulfate

HSD17B10 encodes 3-hydroxyacyl-CoA dehydrogenase type II

Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions

DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing The predominant isoformThis 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.