CLN5 polyclonal, anti-human, mouse

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.

Synonyms: NCL

Cellular Location: Cytoplasm

Immunogen:
A synthetic peptide of human CLN5

Gene Symbol: CLN5

Gene ID: 1203

Swiss prot: O75503

Calculated MW: 41kDa

Recommended dilution:
WB 1:200-1000, IHC 1:40-200,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.