FGF-11 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene are

Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects

and Rab (see MIM 179508) families

Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene

and COA to ensure the highest quality

FGF-11 Polyclonal Antibody, 50ul ROS/Nitric Oxide Detection Mutations in this gene areFibroblast growth factor 11 encoded by FGF11 is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The function of this gene has not yet been determined. The expression pattern of the mouse homolog implies a role in