ND5 Polyclonal Antibody, 50ul Serological Pipets disease:Defects in GRN are the

disease:Defects in GRN are the cause of ubiquitin-positive frontotemporal dementia (UP-FTD)

Isoform 4 is present in the spermatid and mature sperm

The CC cytokines are secreted proteins characterized by two adjacent cysteines

which subsequently combine as a tetramer to produce haptoglobin

ND5 Polyclonal Antibody, 50ul Serological Pipets disease:Defects in GRN are theMT ND5 is a Protein Coding gene. Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. Diseases associated with MT ND5 include leber hereditary optic neuropathy and melas syndrome.