DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing Mutations in this gene also

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

basic and/or keratinocyte growth factor

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

heparin sulfate

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

DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing Mutations in this gene alsoThis 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.