MYOC Polyclonal Antibody, 20ul Immunology Mutations in PARK2 are known

Mutations in PARK2 are known to cause Parkinson disease and autosomal recessive juvenile Parkinson disease

Family members play essential roles in innate immune response to a wide range of pathogenic organisms| tissue damage and other cellular stresses

With a working volume of 300-400 mL and a large surface area of 1900 cm²

subunit:Interacts with FGF1

leading to its inactivation

MYOC Polyclonal Antibody, 20ul Immunology Mutations in PARK2 are knownMYOC 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