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

When induced GABARAPL2 is first digested by ATG4 family enzymes to become its mature form: gABARAPL2-I

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

Family members encode type II membrane-bound glycoproteins that appear to have exclusive specificity for the donor substrate UDP-galactose

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

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.