EFHD1 Polyclonal Antibody, 100ul Mammalian Expression They are implicated in a

They are implicated in a number of cellular processes involving alteration of RNA secondary structure

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

A mutation in this gene is associated with young-adult onset of nonsyndromic deafness-64

This gene belongs to the trypsin family of serine proteases and encodes anionic trypsinogen

EFHD1 Polyclonal Antibody, 100ul Mammalian Expression They are implicated in aThis gene encodes a member of the EF hand super family of calcium binding proteins, which are involved in a variety of cellular processes including mitosis, synaptic transmission, and cytoskeletal rearrangement. The protein encoded by this gene is composed of an N terminal disordered region, proline rich elements, two EF hands, and a C terminal coiled coil domain. This protein has been shown to associate with the mitochondrial inner membrane, and in