CHIP Polyclonal Antibody, 100ul Gene Synthesis Its expression is upregulated during

Its expression is upregulated during dendritic cells maturation

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

which catalyze the reversible hydration of carbon dioxide in various biological processes

which comprises the major protein component of aortic medial amyloid (AMA)

CHIP Polyclonal Antibody, 100ul Gene Synthesis Its expression is upregulated duringThis gene encodes a protein containing tetratricopeptide repeat and a U box that functions as a ubiquitin ligase cochaperone. The encoded protein binds to and ubiquitinates shock cognate 71 kDa protein (Hspa8) and DNA polymerase beta (Polb), among other targets. Mutations in this gene cause spinocerebellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2.