CLN5 rabbit pAb
Ref. EK-ES4682
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
- CLN5; Ceroid-lipofuscinosis neuronal protein 5; Protein CLN5
ceroid-lipofuscinosis, neuronal 5(CLN5) Homo sapiens 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.[provided by RefSeq, Oct 2008],
Chemical properties
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