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SPT6H Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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SPT6H Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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Description

Mutations in this gene are associated with slow-channel congenital myasthenic syndrome

The encoded protein is central to the development of pancreatic cell lineages and may also be required for motor neuron generation

The second activity is restricted to lactating mammary tissues where the enzyme forms a heterodimer with alpha-lactalbumin to catalyze UDP-galactose + D-glucose <=> UDP + lactose

It is active on peptide linkages involving the carboxyl group of lysine or arginine

characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD)

SPT6H Rabbit Polyclonal Antibody, 20ul Apoptosis & Autophagy Mutations in this gene are

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