DAAM1 Polyclonal Antibody, 100ul Nucleic Acid Extraction Mutations in this gene are

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

MELK (Maternal Embryonic Leucine Zipper Kinase) is a Protein Coding gene

this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells

May play a role as a negative regulator of cell growth

This gene is closely linked with two other apolipoprotein genes on chromosome 11

DAAM1 Polyclonal Antibody, 100ul Nucleic Acid Extraction Mutations in this gene areCell motility, adhesion, cytokinesis, and other functions of the cell cortex are mediated by reorganization of the actin cytoskeleton and several formin homology (FH) proteins have been associated with these processes. The protein encoded by this gene contains two FH domains and belongs to a novel FH protein subfamily implicated in cell polarity. A key regulator of cytoskeletal architecture, the small GTPase Rho, is activated during development by Wnt