WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification The encoded protein is widely

The encoded protein is widely distributed among animals and cleaves DNA at GC tracts

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

Muscle contraction

Mutations in this gene result in one form of autosomal dominant hearing impairment

May be involved in necrotic or autophagic cell death

WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification The encoded protein is widelyThis gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly his and trp asp (GH WD) which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression signal transduction apoptosis and gene regulation. This gene is highly expressed in