AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification Mutations in this gene are

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

The FZD1 transcript is expressed in various tissues

2006 [PubMed 17054726])

|subcellular location:Associated with the mitochondrial membrane

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

AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification Mutations in this gene areAmCyan 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.