CLN6 Polyclonal Antibody

Background:
ceroid-lipofuscinosis, neuronal 6, late infantile, variant(CLN6) 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],

Alternative Names:
CLN6, Ceroid-lipofuscinosis neuronal protein 6, Protein CLN6

Immunogen: The antiserum was produced against synthesized peptide derived from human CLN6. AA range:221-270

Isotype: Rabbit

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration: 1 mg/ml

Observed band: 40

GeneID: CLN6

Storage: -20°C/1 year

NOTE: For Research Use Only