This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5 to 3 direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
25 ug of the indicated Human whole cell extracts was loaded onto a 12% SDS-PAGE gel. 1 ug/mL of the antibody was used in this experiment. An isoform containing the peptide sequence is present at ~60 kDa.
Host: Rabbit Target Name: PEO1 Sample Type: Hela Lane A: Primary Antibody Lane B: Primary Antibody + Blocking Peptide Primary Antibody Concentration: 1ug/ml Peptide Concentration: 5.0 ug/ml Lysate Quantity: 25ug/lane/lane Gel Concentration: 12%C10orf2 is supported by BioGPS gene expression data to be expressed in Hela
Host: Rabbit Target: C10ORF2 Positive control (+): HepG2 (HG) Negative control (-): Human stomach (ST) Antibody concentration: 1ug/ml