MYO1A Polyclonal Antibody, 20ul Cell Senescence an autosomal recessive disease associated

an autosomal recessive disease associated with a susceptibility to pyogenic infections

which is important in a wide range of cellular activities: neuronal

It contains an F-box motif and seven conserved helicase motifs| and has both DNA-dependent ATPase and DNA unwinding activities

The encoded protein is postranslationally glycosylated and localized to the lysosome

This gene is a member of the insulin-like growth factor binding protein (IGFBP) family and encodes a protein with an IGFBP domain and a thyroglobulin type-I domain

MYO1A Polyclonal Antibody, 20ul Cell Senescence an autosomal recessive disease associatedThis gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin 1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin based molecular motors. Mutations in this gene have been associated with autosomal