NDUFV2 Polyclonal Antibody, 20ul Low retention tips encoded by the CLIC4 gene

encoded by the CLIC4 gene

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

Synbio Technologies is able to provide a series of recombinant antibody preparation services in diverse forms

5mL adapter

Increased expression of this gene was observed in renal

NDUFV2 Polyclonal Antibody, 20ul Low retention tips encoded by the CLIC4 geneThe 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