Cadherin-26 Polyclonal Antibody, 20ul Fluorescent Staining Deficiency of the muscle-specific enzyme

Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human

It is located in the cytosol and expressed exclusively in brain

5ml tubes in a 2ml rotor

and in vivo effect time of peptides

Mutations in this gene may be associated with dentinogenesis imperfect and autosomal dominant amylogenesis imperfect

Cadherin-26 Polyclonal Antibody, 20ul Fluorescent Staining Deficiency of the muscle-specific enzymeCadherins are a family of adhesion molecules that mediate Ca2+ dependent cell cell adhesion in all solid tissues and modulate a wide variety of processes, including cell polarization and migration. Cadherin domains occur as repeats in the extracellular region and are thought to contribute to the sorting of heterogeneous cell types and the maintenance of orderly structures such as epithelium. CDH26 encodes a cadherin domain containing protein whose