CLN6 Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: RA23551-50, RA23551-100
Citations, Manuals and MSDS Available upon request.
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],
Condition: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage Instructions: -20°C/1 year
Recommended dilutions: Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Alternative Names: CLN6; Ceroid-lipofuscinosis neuronal protein 6; Protein CLN6
Applications: WB; IHC-p; IF (paraffin section) ; ELISA
Species Cross-Reactivity: Human; Rat; Mouse
GeneID (Human): 54982
Protein MW (KDa): 40
SWISS: Q9NWW5
Source: Rabbit
Research Use Only