AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification 2006 [PubMed 17054726])

2006 [PubMed 17054726])

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

one helicase C-terminal domain and one KH domain

Another variant encoding an N-terminally truncated isoform has been reported

AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification 2006 [PubMed 17054726])AmCyan has been adapted from the corresponding full length cDNA for higher solubility, brighter emission, and rapid chromophore maturation (8C12 hours). AmCyan1 has been human codon optimized for enhanced translation in mammalian cells. AmCyan is a very good blue fluorescent reporter protein, and useful in two color analyses with DsRed2, DsRed Express, or AsRed2, and in three color analyses with ZsYellow and HcRed.