EPAS-1 Polyclonal Antibody, 20ul Sealing Film Mutations in COL5A3 are thought

Mutations in COL5A3 are thought to be responsible for the symptoms of a subset of patients with Ehlers-Danlos syndrome type III

Prevents nuclear translocation of nuclear factor of activated T-cell to the nucleus

and EPHA7 receptors

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EPAS-1 Polyclonal Antibody, 20ul Sealing Film Mutations in COL5A3 are thoughtEPAS1 encodes a transcription factor involved in the induction of genes regulated by oxygen, which is induced as oxygen levels fall. The endothelial PAS domain protein 1 contains a basic helix loop helix domain protein dimerization domain as well as a domain found in proteins in signal transduction pathways which respond to oxygen levels. Mutations in this gene are associated with erythrocytosis familial type 4.