FAK(Phospho Tyr861) Polyclonal Antibody, 50ul Custom DNA Oligos Mutations in DCLRE1C can cause

Mutations in DCLRE1C can cause Athabascan-type severe combined immunodeficiency (SCIDA) and Omenn syndrome

P311 regulates retinoic-acid lipid-droplet biogenesis

Also detected in hepatoblastoma HepG2 cells

and SRF) box superfamily of transcription factors

FAK(Phospho Tyr861) Polyclonal Antibody, 50ul Custom DNA Oligos Mutations in DCLRE1C can causeThis gene encodes a cytoplasmic protein tyrosine kinase which is found concentrated in the focal adhesions that form between cells growing in the presence of extracellular matrix constituents. The encoded protein is a member of the FAK subfamily of protein tyrosine kinases but lacks significant sequence similarity to kinases from other subfamilies. Activation of this gene may be an important early step in cell growth and intracellular signal