NMD3 Rabbit Polyclonal Antibody, 100ul Recombinant Protein Mutations in CHAT are associated

Mutations in CHAT are associated with congenital myasthenic syndrome associated with episodic apnea

forming inactive G-protein heterotrimers

Mutations in this gene have been associated with Andersen syndrome

ATF1 encodes an activating transcription factor

NMD3 Rabbit Polyclonal Antibody, 100ul Recombinant Protein Mutations in CHAT are associatedRibosomal 40S and 60S subunits associate in the nucleolus and are exported to the cytoplasm. The protein encoded by this gene is involved in the passage of the 60S subunit through the nuclear pore complex and into the cytoplasm. Several transcript variants exist for this gene but the full length natures of only two have been described to date.