CLN5 anticorps (AA 171-220)

N° du produit ABIN1451151

Cet anticorps anti-CLN5 Polyclonal Lapin (ABIN1451151) détecte spécifiquement CLN5 dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour CLN5 anticorps (AA 171-220) (ABIN1451151)

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

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLN5 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-CLN5 anticorps

Épitope: AA 171-220

Fonction: CLN5 Antibody

Specificité: 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.

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

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur CLN5

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

Autre désignation: CLN5

Sujet:

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

Poids moléculaire: 46 kDa

ID gène: 1203

OMIM: 256731

UniProt: O75503