GAP-43 Monoclonal Antibody(Mix), 20ul Plates & Dishes Mutations in this gene cause

Mutations in this gene cause corneal fleck dystrophy (CFD)

Heterogeneous nuclear ribonucleoprotein L is among the proteins that are stably associated with hnRNP complexes and along with other hnRNP proteins is likely to play a major role in the formation

Its role in the regulation of normal mitochondrial function and in disease states attributed to mitochondrial dysfunction is not known

Each pack contains 1 L of concentrated solution and can be stored at room temperature

GAP-43 Monoclonal Antibody(Mix), 20ul Plates & Dishes Mutations in this gene causeThe protein encoded by this gene has been termed a 'growth' or 'plasticity' protein because it is expressed at high levels in neuronal growth cones during development and axonal regeneration. This protein is considered a crucial component of an effective regenerative response in the nervous system. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.