GSTM1 Polyclonal Antibody, 100ul Cell Function Analysis disease:Defects in MT-ND2 are a

disease:Defects in MT-ND2 are a cause of Leber hereditary optic neuropathy (LHON)

Overexpression of this gene has been shown to induce apoptosis in cells

The encoded protein is part of the integrin-linked kinase signaling complex and plays a role in cell adhesion| motility and survival

tissue specificity:Expressed in brain and testis

GSTM1 Polyclonal Antibody, 100ul Cell Function Analysis disease:Defects in MT-ND2 are aCytosolic and membrane bound forms of glutathione S transferase are encoded by two distinct supergene families. At present, eight distinct classes of the soluble cytoplasmic mammalian glutathione S transferases have been identified: alpha, kappa, mu, omega, pi, sigma, theta and zeta. This gene encodes a glutathione S transferase that belongs to the mu class. The mu class of enzymes functions in the detoxification of electrophilic compounds, including