CLN5 产品
(Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
Categories
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].
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Featured CLN5 Categories
Recommended CLN5 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
ELISA, IHC, IF
Validations
- (3)
Cat. No.
ABIN7147493
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, IHC
Validations
- (2)
Cat. No.
ABIN7256432
Quantity
200 μL
Datasheet
Datasheet
Reactivity
Human, Mouse, Rat
Application
WB, ELISA, IF, ICC
Validations
- (2)
Cat. No.
ABIN6259553
Quantity
100 μL
Datasheet
Datasheet
Recommended CLN5 蛋白
Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Source
HEK-293 Cells
Validations
- (1)
Cat. No.
ABIN2713927
Quantity
20 μg
Datasheet
Datasheet
Synonyms and alternative names related to CLN5
CLN5, intracellular trafficking protein (CLN5), ceroid-lipofuscinosis, neuronal 5 (Cln5), CLN5, intracellular trafficking protein (Cln5), A730075N08Rik, NCLProtein level used designations for CLN5
- ceroid-lipofuscinosis neuronal protein 5
- ceroid-lipofuscinosis neuronal protein 5 homolog
- ceroid-lipofuscinosis neuronal 5
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