Fhit Polyclonal Antibody, 50ul[BT-AP03231] Fluorescent Staining Diseases associated with SV2C include

Diseases associated with SV2C include alcohol-related birth defect and foodborne botulism

a receptor subunit also shared by many other cytokines

Mutations in this gene have been associated with bone marrow failure syndrome 2

Binding of YWHAZ inhibits DNA-binding

bronchial and small airway lung epithelial cells

Fhit Polyclonal Antibody, 50ul[BT-AP03231] Fluorescent Staining Diseases associated with SV2C includeFHIT, a member of the histidine triad gene family, encodes a diadenosine 5',5''' P1,P3 triphosphate hydrolase involved in purine metabolism. The gene encompasses the common fragile site FRA3B on chromosome 3, where carcinogen induced damage can lead to translocations and aberrant transcripts of this gene. In fact, aberrant transcripts from this gene have been found in about half of all esophageal, stomach, and colon carcinomas. Alternatively spliced