VGLL1 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions and neonatal lethality

and neonatal lethality

controlling the alpha-1 subunit membrane targeting and shifting the voltage dependence of activation and inactivation

|Contains 1 SH2 domain

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

Mutations in this gene have been found in some patients with the CHARGE syndrome

VGLL1 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions and neonatal lethalityThe 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.