Background：This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses （NCL）. Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.
仕様
Synonyms：Ceroid lipofuscinosis neuronal 5,Ceroid-lipofuscinosis neuronal protein 5,CLN5,CLN5,NCL,Protein CLN5
Host：Rabbit
Reactivity：Human,Mouse,Rat
Applications：WB
Concentration：1mg/ml
Immunogen：Recombinant protein of human CLN5
Purification Method：Affinity purification
Clonality：Polyclonal
Conjugation：Unconjugated
Buffer：Buffer： PBS with 0.02％ sodium azide, 50％ glycerol, pH7.3.
