FGF-17 Polyclonal Antibody, 100ul Nucleic Acid Amplification an endogenous toxin derived from

an endogenous toxin derived from the fermentation of tryptophan

Defects in this gene are a cause of Leigh syndrome

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate

Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses

This gene is identified by the similarity of its product to the N-terminal region of BCL7A protein

FGF-17 Polyclonal Antibody, 100ul Nucleic Acid Amplification an endogenous toxin derived fromFGF17 encodes a member of the fibroblast growth factor (FGF) family. Member of the FGF family 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. Fibroblast growth factor 17 is expressed during embryogenesis and in the adult cerebellum and cortex and may be essential for vascular growth and