DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing heparin sulfate

heparin sulfate

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

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

The predominant isoform

including small cell lung carcinoma and renal cell carcinoma

DLL3 Polyclonal Antibody, 100ul Microbial Genome Editing heparin sulfateThis 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.