Myosin VI anticorps

N° du produit ABIN7256548

Détail du produit anti-Myosin VI anticorps

Antigène: Myosin VI (MYO6)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Myosin VI est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human MYO6 (NP_004990.3).

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000 IF 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur Myosin VI

Antigène: Myosin VI (MYO6)

Autre désignation: MYO6 (MYO6 Produits)

Synonymes: anticorps 95F, anticorps 95F MHC, anticorps CG5695, anticorps Dm 95F, anticorps Dm95F, anticorps Dmel\\CG5695, anticorps Dro95F, anticorps JAG, anticorps Jaguar, anticorps Jar, anticorps M6, anticorps MHC95F, anticorps MYOVI, anticorps Mhc95F, anticorps MyoVI, anticorps Myosin VI, anticorps jag, anticorps ms(3)06746, anticorps myosins VI, anticorps DFNA22, anticorps DFNB37, anticorps BC029719, anticorps Tlc, anticorps sv, anticorps RGD1560646, anticorps CMY6, anticorps jaguar, anticorps myosin VI, anticorps jar, anticorps LOC373230, anticorps MYO6, anticorps myo6, anticorps Myo6

Sujet: This gene encodes a reverse-direction 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.

Poids moléculaire:

Observed_MW: 150 kDa

Calculated_MW: 145 kDa/146 kDa/148 kDa/149 kDa

ID gène: 4646

UniProt: Q9UM54

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