WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in MTR have been

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

and IL1RL1 (T1/ST2)

The protein is involved in maintaining blood pressure and in the pathogenesis of essential hypertension and preeclampsia

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

Muscle contraction

WDR33 Rabbit Polyclonal Antibody, 50ul Protein Post-translational Modification Mutations in MTR have beenThis 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