MB211 Rabbit Polyclonal Antibody, 100ul Drug Development and Evaluation Mutations that result in a

Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy

It is composed of a dimer of disulfide-linked heavy and light chains

is normally found in the cytoplasm

Phosphorylation of S6 leads to an increase in protein synthesis and cell proliferation

MB211 Rabbit Polyclonal Antibody, 100ul Drug Development and Evaluation Mutations that result in aThis gene is similar to the MAB 21 cell fate determining gene found in C. elegans. It may be involved in eye and cerebellum development and it has been proposed that expansion of a trinucleotide repeat region in the 5' UTR may play a role in a variety of psychiatric disorders.