c-Myc(Phospho Thr58) Polyclonal Antibody, 100ul Drying & Desiccation A mutation in this gene

A mutation in this gene may be associated with increased risk for Barrett's esophagus and esophageal adenocarcinoma

Mutations in this gene are associated with atypical hemolytic uremic syndrome and age-related macular degeneration in human patients

FSCN1 encodes a member of the fascin family of actin-binding proteins

p32 is mainly found in the cytoplasm

Members of the WIPI subfamily of WD40 repeat proteins have a 7-bladed propeller structure and contain a conserved motif for interaction with phospholipids

c-Myc(Phospho Thr58) Polyclonal Antibody, 100ul Drying & Desiccation A mutation in this geneThe protein encoded by this gene is a multifunctional, nuclear phosphoprotein that plays a role in cell cycle progression, apoptosis and cellular transformation. It functions as a transcription factor that regulates transcription of specific target genes. Mutations, overexpression, rearrangement and translocation of this gene have been associated with a variety of hematopoietic tumors, leukemias and lymphomas, including Burkitt lymphoma. There is