VGLL1 Rabbit Polyclonal Antibody, 100ul Lentiviral Packaging a rare autosomal recessive disorder

a rare autosomal recessive disorder

These two genes are frequently deleted or altered in neuroblastoma

Designed with a conical bottom

EPHB6 encodes a member of a family of transmembrane proteins that function as receptors for ephrin-B family proteins

The protein kinase D2 encoded by PRKD2 belongs to the protein kinase D (PKD) family of serine/threonine protein kinases

VGLL1 Rabbit Polyclonal Antibody, 100ul Lentiviral Packaging a rare autosomal recessive disorderThe protein encoded by this gene binds proteins of the TEA domain family of transcription factors (TEFs) through the Vg (vestigial) homology region found in its N terminus. It may thus function as a specific coactivator for the mammalian TEFs.