Ribosomal Protein S3 Polyclonal Antibody, 100ul Buffer Solutions Mutations in this gene are

Mutations in this gene are associated with succinyl CoA:3-oxoacid CoA transferase deficiency

especially in podosome rearrangement and reorganization of the actin cytoskeleton

also known as testotoxicosis

Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

No other information about TUSC2 is currently available

Ribosomal Protein S3 Polyclonal Antibody, 100ul Buffer Solutions Mutations in this gene areRibosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. RPS3 encodes a ribosomal protein that is a component of the 40S subunit, where it forms part of the domain where translation is initiated. 40S ribosomal protein S3 belongs to the S3P family of ribosomal proteins. Studies of the mouse