DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing Variation at this gene has

Variation at this gene has been observed in patients with absorptive hypercalciuria

hoA) specifically interacted with the myosin-binding subunit (MBS) of myosin phosphatase

HSD17B10 encodes 3-hydroxyacyl-CoA dehydrogenase type II

The predominant isoform

basic and/or keratinocyte growth factor

DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing Variation at this gene hasThis 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.