c-Abl Rabbit Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in CTSA are associated

Mutations in CTSA are associated with galactosialidosis

Mutations in this gene are associated with orofacial cleft and microphthalmia in human patients

the protein encoded by TSPO (translocator protein) interacts with some benzodiazepines and has different affinities than its endogenous counterpart

but not for neutrophils

Mutations in this gene have been associated with thrombophilia due to protein C deficiency| neonatal purpura fulminans| and recurrent venous thrombosis

c-Abl Rabbit Polyclonal Antibody, 100ul Pathway and Network Analysis Mutations in CTSA are associatedThis gene is a protooncogene that encodes a protein tyrosine kinase involved in a variety of cellular processes, including cell division, adhesion, differentiation, and response to stress. The activity of the protein is negatively regulated by its SH3 domain, whereby deletion of the region encoding this domain results in an oncogene. The ubiquitously expressed protein has DNA binding activity that is regulated by CDC2 mediated phosphorylation,