HRF Polyclonal Antibody, 50ul Vessels Binds to cells

Binds to cells

DMD patients carry mutations which cause premature translation termination (nonsense or frame shift mutations)

Mutations in this gene may be associated with congenital aural atresia syndrome

The encoded protein positively regulates Notch signaling by ubiquitinating the Notch receptors

Belongs to the Mo25 family

HRF Polyclonal Antibody, 50ul Vessels Binds to cellsTPT1 is a Protein Coding gene. Translationally Controlled 1 is a tumor protein, involved in calcium binding and microtubule stabilization. Diseases associated with TPT1 include urticaria and allergic hypersensitivity disease. Among its related pathways are PLK1 signaling events. Gene Ontology (GO) annotations related to this gene include poly(A) RNA binding and transcription factor binding.