ATL1 anticorps (AA 24-552) (Fluoro594)

N° du produit ABIN7970715

Cet anticorps Lapin Polyclonal détecte spécifiquement ATL1 dans FACS. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour ATL1 anticorps (AA 24-552) (Fluoro594) (ABIN7970715)

Antigène: ATL1 (Atlastin GTPase 1 (ATL1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ATL1 est conjugé à/à la Fluoro594

Application: Flow Cytometry (FACS)

Détail du produit anti-ATL1 anticorps (Fluoro594)

Épitope: AA 24-552

Fonction: Anti-ATL1 Antibody Fluoro594 Conjugated

Homologie: Human ATL1 shares 97.5%,98.3% amino acid (aa) sequence identity with mouse,rat ATL1,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human ATL1 recombinant protein (Position: E24-Q552). Human ATL1 shares 97.5% and 98.3% amino acid (aa) sequence identity with mouse and rat ATL1, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur ATL1

Antigène: ATL1 (Atlastin GTPase 1 (ATL1))

Autre désignation: ATL1

Sujet:

Background: Atlastin, or Atlastin-1, is a protein that in humans is encoded by the ATL1 gene. The protein encoded by this gene is a GTPase and a Golgi body transmembrane protein. The encoded protein can form a homotetramer and has been shown to interact with spastin and with mitogen-activated protein kinase kinase kinase kinase 4. This protein may be involved in axonal maintenance as evidenced by the fact that defects in this gene are a cause of spastic paraplegia type 3. Three transcript variants encoding two different isoforms have been found for this gene.

Gene Full Name: atlastin GTPase 1

ID gène: 51062

UniProt: Q8WXF7