HRF Polyclonal Antibody, 50ul Vessels DMD patients carry mutations which

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

The protein encoded by this gene belongs to the actin family of proteins| which are highly conserved proteins that play a role in cell motility| structure and integrity

Binds to cells

but upstream of CASP3/caspase-3 as well as CCND1/cyclin D1 and E2F1

HRF Polyclonal Antibody, 50ul Vessels DMD patients carry mutations whichTPT1 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.