AHI1 anticorps (N-Term)

N° du produit ABIN2854592

L’anticorps Lapin Polyclonal anti-AHI1 a été validé pour WB. Il convient pour détecter AHI1 dans des échantillons de Humain.

Aperçu rapide pour AHI1 anticorps (N-Term) (ABIN2854592)

Antigène: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp AHI1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-AHI1 anticorps

Épitope: N-Term

Réactivité croisée: Humain

Attributs du produit: Rabbit Polyclonal antibody to AHI1 (Abelson helper integration site 1)
AHI1 antibody [N1], N-term

Purification: Purified by antigen-affinity chromatography.

Immunogène: Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human AHI1. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: NT2D1

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur AHI1

Antigène: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Autre désignation: Abelson helper integration site 1

Sujet: This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified.

Poids moléculaire: 137 kDa

ID gène: 54806

UniProt: Q8N157