Myosin VI anticorps (AA 383-786) (Fluoro488)

N° du produit ABIN8012800

Cet anticorps anti-Myosin VI Polyclonal Lapin conjugué à Fluoro488 (ABIN8012800) détecte spécifiquement Myosin VI dans FACS. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour Myosin VI anticorps (AA 383-786) (Fluoro488) (ABIN8012800)

Antigène: Myosin VI (MYO6)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Myosin VI est conjugé à/à la Fluoro488

Application: Flow Cytometry (FACS)

Détail du produit anti-Myosin VI anticorps (Fluoro488)

Épitope: AA 383-786

Fonction: Anti-MYO6 Antibody Fluoro488 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human MYO6 recombinant protein (Position: Q383-H786).

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 Myosin VI

Antigène: Myosin VI (MYO6)

Autre désignation: MYO6

Sujet:

Background: Unconventional myosin-VI, is a protein that in humans is coded for by MYO6. This gene encodes a reverse-ion motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Gene Full Name: myosin VI

ID gène: 4646

UniProt: Q9UM54

Pathways: Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization