NIPA2 Rabbit Polyclonal Antibody, 50ul Stepper autosomal recessive inclusion body myopathy

autosomal recessive inclusion body myopathy

Pseudogenes of this gene have been defined on chromosomes 1

This gene encodes a member of a family of p21-stimulated serine/threonine protein kinases

but not glycoproteins undergoing productive folding

Eukaryotic translation initiation factor 2 (EIF-2) functions in the early steps of protein synthesis by forming a ternary complex with GTP and initiator tRNA and binding to a 40S ribosomal subunit

NIPA2 Rabbit Polyclonal Antibody, 50ul Stepper autosomal recessive inclusion body myopathyThis gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3 7 and 21.