CLN8 Polyclonal Antibody, 50ul Transporters pyrogen-free

pyrogen-free

|disease:Defects in CTSC are a cause of Haim-Munk syndrome (HMS)

With 25ml capacity and precise 2/10ml graduations

The protein encoded by this gene belongs to the leucine-rich repeat superfamily

Mutations in this gene have been associated with autosomal recessive limb-girdle muscular dystrophy and dilated cardiomyopathy

CLN8 Polyclonal Antibody, 50ul Transporters pyrogen-freeThis gene encodes a transmembrane protein belonging to a family of proteins containing TLC domains, which are postulated to function in lipid synthesis, transport, or sensing. The protein localizes to the endoplasmic reticulum (ER), and may recycle between the ER and ER Golgi intermediate compartment. Mutations in this gene are associated with progressive epilepsy with mental retardation (EMPR), which is a subtype of neuronal ceroid lipofuscinoses