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A suggested positive control is human liver tissue lysate.
PA5-20915 can be used with blocking peptide PEP-1029.
TMEM70 is a recently identified mitochondrial protein that is thought to play a role in the biogenesis of the ATP synthase in higher eukaryotes. Mutations in this gene result in early neonatal onset of hypotonia, hypertrophic cardiomyopathy, lactic acidos and 3-methylglutaconic aciduria (3-MGC-uria), and usually cause death within the first six weeks of life, although some patients survive much longer. Little is known of the role of TMEM70, but it is conserved across multicellular eukaryotic organisms. It contains a conserved DUF1301 domain and two putative transmembrane regions.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Transmembrane protein 70, mitochondrial
基因别名: 1110020A09Rik; 2210416J16Rik; MC5DN2; RGD1566224; TMEM70
UniProt ID: (Human) Q9BUB7, (Mouse) Q921N7
Entrez Gene ID: (Human) 54968, (Mouse) 70397, (Rat) 500384