NDUFV2 Polyclonal Antibody, 50ul Monoclonal Antibody Preparation 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)

10 µm PVDF membrane

Annexin A2 functions as an autocrine factor which heightens osteoclast formation and bone resorption

PTM:Auto-ubiquitinated upon EGF-mediated cell activation or upon T-cell costimulation by CD28

NDUFV2 Polyclonal Antibody, 50ul Monoclonal Antibody Preparation Mutations in this gene areThe NADH ubiquinone oxidoreductase complex (complex I) of the mitochondrial respiratory chain catalyzes the transfer of electrons from NADH to ubiquinone, and consists of at least 43 subunits. The complex is located in the inner mitochondrial membrane. NDUFV2 encodes the 24 kDa subunit of complex I, and is involved in electron transfer. Mutations in this gene are implicated in Parkinson's disease, bipolar disorder, schizophrenia, and have been found