DHHC-15 Polyclonal Antibody, 20ul Plasmid Preparation Mutations in CTSD play a

Mutations in CTSD play a causal role in neuronal ceroid lipofuscinosis-10 and may be involved in the pathogenesis of several other diseases

Multiple cellular activities have been attributed to the encoded protein

Marfan Syndrome

and elevated levels of the muscle form of creatine kinase in serum

The protein encoded by DYSF (dysferlin) belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma

DHHC-15 Polyclonal Antibody, 20ul Plasmid Preparation Mutations in CTSD play aZinc finger DHHC type containing 15 encoded by ZDHHC15 belongs to the DHHC palmitoyltransferase family. Mutations in this gene are associated with mental retardatio X linked type 91 (MRX91). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.