Atrophin 1 anticorps (AA 50-130)

N° du produit ABIN7213736

Cet anticorps Lapin Polyclonal détecte spécifiquement Atrophin 1 dans WB et ELISA. Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour Atrophin 1 anticorps (AA 50-130) (ABIN7213736)

Antigène: Atrophin 1 (ATN1)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Atrophin 1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Atrophin 1 anticorps

Épitope: AA 50-130

Fonction: Atrophin-1 Polyclonal Antibody

Specificité: Atrophin-1 Polyclonal Antibody detects endogenous levels of Atrophin-1 protein.

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

Immunogène: Synthesized peptide derived from the N-terminal region of human Atrophin-1 at AA range: 50-130

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000). Not yet tested in other applications.

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 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: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Détails sur Atrophin 1

Antigène: Atrophin 1 (ATN1)

Autre désignation: Atrophin-1

Sujet: Rabbit Anti-Atrophin-1 Polyclonal Antibody,ATN1, D12S755E, DRPLA, Atrophin-1, Dentatorubral-pallidoluysian atrophy protein,Dentatorubral pallidoluysian atrophy (DRPLA) is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion from 7-35 copies to 49-93 copies of a trinucleotide repeat (CAG/CAA) within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat. Alternative splicing results in two transcripts variants that encode the same protein.,Atrophin-1

ID gène: 1822

UniProt: P54259