CLN6 Antibody
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


CLN6 Antibody
Background:
CLN6 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 CLN6 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.NCBI Gene ID:
54982Swiss Prot:
Q9NWW5Accession Number:
NP_060352Host:
RabbitReactivity:
Human, Mouse, Rat, DogImmunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human CLN6.Clonality:
PolyclonalConjugation:
UnconjugatedType:
Primary AntibodiesField of Research:
MembranePurification:
Antibody is purified by peptide affinity chromatography method.Positive Control:
Cat. No. XBL-10410 - Fetal Lung Tissue LysateConcentration:
Batch dependentBuffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.Modification:
NoneShipping Conditions:
Blue IceStorage Conditions:
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store CLN6 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.Calculated Molecular Weight:
36 kDaApplications Notes:
CLN6 antibody can be used for detection of CLN6 by ELISA at 1:1562500. CLN6 antibody can be used for detection of CLN6 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.Symbol:
CLN6NCBI Official Name:
Ceroid-lipofuscinosis, neuronal 6, late infantile, variantNCBI Organism:
Homo sapiensBackground Reference 01:
Heine, C., (2007) Mol. Membr. Biol. 24 (1), 74-87.Other Product Names:
CLN6, FLJ20561, HsT18960, nclf, CLN4ATested Applications:
ELISA, WBProtein ID:
8923532Physical Properties:
Liquid
