TTYH2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries disease progression

disease progression

Both this protein and E2F4 interact with tumor suppressor proteins p130 and p107

Defects in this gene are the cause of glycogen storage disease II| also known as Pompe's disease| which is an autosomal recessive disorder with a broad clinical spectrum

S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells| and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation

TTYH2 Rabbit Polyclonal Antibody, 20ul Human Genome Knockout Libraries disease progressionThis gene encodes a member of the tweety family of proteins. Members of this family function as chloride anion channels. The encoded protein functions as a calcium(2+) activated large conductance chloride( ) channel and may play a role in kidney tumorigenesis. Two transcript variants encoding distinct isoforms have been identified for this gene.