AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification ISL2 is a Protein Coding

ISL2 is a Protein Coding gene

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

|subcellular location:Associated with the mitochondrial membrane

The FZD1 transcript is expressed in various tissues

This CA1 (carbonic anhydrase 1) gene is closely linked to the CA2 and CA3 genes on chromosome 8

AmCyan Polyclonal Antibody, 20ul[BT-AP06220] Protein Post-translational Modification ISL2 is a Protein CodingAmCyan 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.