CLN5 antibody (AA 171-220)

Catalog No. ABIN1451151

The Rabbit Polyclonal anti-CLN5 antibody (ABIN1451151) specifically detects CLN5 in WB and ELISA. The antibody is reactive with Human, Rat and Mouse samples.

Quick Overview for CLN5 antibody (AA 171-220) (ABIN1451151)

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CLN5 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-CLN5 Antibody

Binding Specificity: AA 171-220

Purpose: CLN5 Antibody

Specificity: CLN5 Polyclonal Antibody detects endogenous levels of CLN5 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: The antiserum was produced against synthesized peptide derived from human CLN5. AA range:171-220

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for CLN5

Target: CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))

Alternative Name: CLN5

Background:

Synonyms: CLN5, Ceroid-lipofuscinosis neuronal protein 5, Protein CLN5

Background: ceroid-lipofuscinosis, neuronal 5(CLN5) 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],

Gene Name: CLN5

Protein Name: Ceroid-lipofuscinosis neuronal protein 5

Molecular Weight: 46 kDa

Gene ID: 1203

OMIM: 256731

UniProt: O75503