MYO5A anticorps (C-Term)

N° du produit ABIN7467586

L’anticorps Lapin Polyclonal anti-MYO5A a été validé pour WB. Il convient pour détecter MYO5A dans des échantillons de Humain.

Aperçu rapide pour MYO5A anticorps (C-Term) (ABIN7467586)

Antigène: MYO5A (Myosin VA (MYO5A))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYO5A est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-MYO5A anticorps

Épitope: C-Term

Réactivité croisée: Humain

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the C-terminus region of human MYO5A. 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: U87-MG , SK-N-SH

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.84 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: 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 MYO5A

Antigène: MYO5A (Myosin VA (MYO5A))

Autre désignation: myosin VA

Sujet: Myosin VA , GS1 , MYH12 , MYO5 , MYR12,This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq]

Poids moléculaire: 215 kDa

ID gène: 4644

UniProt: Q9Y4I1

Pathways: Hormone Transport, Peptide Hormone Metabolism