Cytokeratin 15 Monoclonal Antibody, 100ul Apoptosis & Autophagy Defects in this gene are

Defects in this gene are a cause of pyruvate dehydrogenase deficiency which results in neurological dysfunction and lactic acidosis in infancy and early childhood

and is involved in essential cellular functions

Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones

RPS4Y1 encodes ribosomal protein S4

Alternatively spliced transcript variants encoding different isoforms have been described but the full-length nature of all of them has yet to be determined

Cytokeratin 15 Monoclonal Antibody, 100ul Apoptosis & Autophagy Defects in this gene areThe protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains and are clustered in a region on chromosome 17q21. 2.