Choline Acetyltransferase anticorps (AA 19-612)

N° du produit ABIN7871600

Cet anticorps Lapin Polyclonal détecte spécifiquement Choline Acetyltransferase dans WB, ELISA et IHC (p). Il présente une réactivité avec des échantillons de Souris et Rat.

Aperçu rapide pour Choline Acetyltransferase anticorps (AA 19-612) (ABIN7871600)

Antigène: Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Choline Acetyltransferase est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-Choline Acetyltransferase anticorps

Épitope: AA 19-612

Fonction: Chat Antibody / Choline Acetyltransferase

Purification: Affinity purified

Immunogène: Recombinant rat protein (amino acids E19-D612) was used as the immunogen for the CHAT antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the CHAT antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the CHAT antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur Choline Acetyltransferase

Antigène: Choline Acetyltransferase (CHAT) (Choline O-Acetyltransferase (CHAT))

Autre désignation: Chat

Sujet: Choline acetyltransferase (commonly abbreviated as ChAT or CAT) is a transferase enzyme responsible for the synthesis of the neurotransmitter acetylcholine. In humans, the choline acetyltransferase enzyme is encoded by the CHAT gene. This gene product is a characteristic feature of cholinergic neurons, and changes in these neurons may explain some of the symptoms of Alzheimer's disease. Polymorphisms in this gene have been associated with Alzheimer's disease and mild cognitive impairment. Mutations in this gene are associated with congenital myasthenic syndrome associated with episodic apnea. Multiple transcript variants encoding different isoforms have been found for this gene, and some of these variants have been shown to encode more than one isoform.

UniProt: P32738

Pathways: Skeletal Muscle Fiber Development