EYA1/EYA4 Polyclonal Antibody, 20ul Custom Peptide Synthesis This gene consists of two

This gene consists of two exons and encodes a 104aa protein

Because of their central role in linking amino acids with nucleotide triplets contained in tRNAS

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

1 Units/μL of yeast-based activity in a convenient 500 μL package

EYA1/EYA4 Polyclonal Antibody, 20ul Custom Peptide Synthesis This gene consists of twoThis gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript