CLN5 anticorps (C-Term)

N° du produit ABIN5517800

Cet anticorps anti-CLN5 Polyclonal Lapin (ABIN5517800) détecte spécifiquement CLN5. L’anticorps est réactif avec des échantillons de Humain, Rat, Boeuf (Vache), Chien, Cobaye, Cheval, Porc et Lapin.

Aperçu rapide pour CLN5 anticorps (C-Term) (ABIN5517800)

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

Reactivité: Humain, Rat, Boeuf (Vache), Chien, Cobaye, Cheval, Porc, Lapin

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CLN5 est non-conjugé

Application: Veuillez nous consulter SVP

Détail du produit anti-CLN5 anticorps

Épitope: C-Term

Fonction: CLN5 Antibody - C-terminal region

Séquence: DNETGIYYET WNVKASPEKG AETWFDSYDC SKFVLRTFNK LAEFGAEFKN

Homologie: Cow: 77%, Dog: 79%, Guinea Pig: 79%, Horse: 86%, Human: 100%, Pig: 86%, Rabbit: 86%, Rat: 79%

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the C terminal region of human CLN5

Information d'application

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP59986-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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.

Conseil sur la manipulation: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur CLN5

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

Autre désignation: CLN5

Sujet:

Background Information: 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.

Gene Name: ceroid-lipofuscinosis, neuronal 5

Alternative Symbols: NCL

Protein Name: ceroid-lipofuscinosis neuronal protein 5

Poids moléculaire: 39 kDa

ID gène: 1203

NCBI Accession: NP_006484

UniProt: O75503