WASL Polyclonal Antibody, 20ul Molecular Sciences Defects in this enzyme are

Defects in this enzyme are associated with osteopetrosis and renal tubular acidosis

a mutagenic base byproduct which occurs as a result of exposure to reactive oxygen

Little or no detectable expression found in pancreas

The protein consists of a tetramer of identical subunits

The expression of different isoforms and splice variants is regulated in a developmental

WASL Polyclonal Antibody, 20ul Molecular Sciences Defects in this enzyme areThis gene encodes a member of the Wiskott Aldrich syndrome (WAS) protein family. Wiskott Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin related protein 2 3