CLN5
ceroid-lipofuscinosis, neuronal 5
Synonymes:
NCL
Espèce(s):
Human CLN5 (1203), Mouse Cln5 (211286), Rat Cln5 (306128), naked mole-rat Cln5 (101715781), Zebrafish cln5 (569407), chicken CLN5 (101752092), dog CLN5 (485498), domestic cat CLN5 (101085427), cow CLN5 (529186), sheep CLN5 (100034668)
ID UniProtKB:
ID du gène:
- Human(1203) Summary: 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]
- Mouse(211286) ceroid-lipofuscinosis, neuronal 5
- Rat(306128) ceroid-lipofuscinosis, neuronal 5
- naked mole-rat(101715781) ceroid-lipofuscinosis, neuronal 5
- Zebrafish(569407) ceroid-lipofuscinosis, neuronal 5
- chicken(101752092) ceroid-lipofuscinosis, neuronal 5
- dog(485498) ceroid-lipofuscinosis, neuronal 5
- domestic cat(101085427) ceroid-lipofuscinosis, neuronal 5
- cow(529186) ceroid-lipofuscinosis, neuronal 5
- sheep(100034668) ceroid-lipofuscinosis, neuronal 5
- domestic guinea pig(100726787) ceroid-lipofuscinosis, neuronal 5
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Antibodies
Référence du produit
Description
Espèces réactives
Application
Anti-CLN5 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
Espèces réactives
human
Application
immunohistochemistry
western blot
western blot