MYOC Polyclonal Antibody, 50ul Custom DNA Oligos Mutation in this gene are

Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome

Fucose is typically found as a terminal modification of branched chain glycoconjugates

The protein encoded by this gene is a membrane protein that can form a non-selective channel permeable to calcium and other cations

growth retardation

VASP may also be involved in the intracellular signaling pathways that regulate integrin-extracellular matrix interactions

MYOC Polyclonal Antibody, 50ul Custom DNA Oligos Mutation in this gene areMYOC encodes the protein myocilin, which is believed to have a role in cytoskeletal function. MYOC is expressed in many occular tissues, including the trabecular meshwork, and was revealed to be the trabecular meshwork glucocorticoid inducible response protein (TIGR). The trabecular meshwork is a specialized eye tissue essential in regulating intraocular pressure, and mutations in MYOC have been identified as the cause of hereditary juvenile onset