C9ORF72 anticorps (AA 400-450)

N° du produit ABIN5688963

Cet anticorps Lapin Polyclonal détecte spécifiquement C9ORF72 dans WB, ELISA et ICC. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour C9ORF72 anticorps (AA 400-450) (ABIN5688963)

Antigène: C9ORF72 (Chromosome 9 Open Reading Frame 72 (C9ORF72))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C9ORF72 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunocytochemistry (ICC)

Détail du produit anti-C9ORF72 anticorps

Épitope: AA 400-450

Specificité: ALSFTD antibody is human, mouse and rat reactive. At least two isoforms are known to exist.

Purification: ALSFTD Antibody is affinity chromatography purified via peptide column.

Immunogène: ALSFTD antibody was raised against a 19 amino acid peptide from near the carboxy terminus of human ALSFTD.

The immunogen is located within amino acids 400 - 450 of ALSFTD.

Isotype: IgG

Information d'application

Indications d'application: ALSFTD antibody can be used for the detection of ALSFTD by Western blot at 1 - 2 μ,g/mL. Antibody can also be used for immunocytochemistry at 10 μ,g/mL.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: ALSFTD Antibody is supplied in PBS containing 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: 4 °C,-20 °C

Stockage commentaire: ALSFTD antibody can be stored at 4°C for three months and -20°C, stable for up to one year.

Détails sur C9ORF72

Antigène: C9ORF72 (Chromosome 9 Open Reading Frame 72 (C9ORF72))

Autre désignation: ALSFTD

Sujet: ALSFTD (C9orf72) is considered to play a role in gender determination (1). Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG (2). Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster (3,4).

Poids moléculaire: Predicted: 53 kDa

Observed: 52 kDa

ID gène: 203228

NCBI Accession: NP_060795

UniProt: Q96LT7