MYO5A anticorps

N° du produit ABIN7264882

Détail du produit anti-MYO5A anticorps

Antigène: MYO5A (Myosin VA (MYO5A))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYO5A est non-conjugé

Application: Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human MYO5A (NP_000250.3).

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:100

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 MYO5A

Antigène: MYO5A (Myosin VA (MYO5A))

Autre désignation: MYO5A (MYO5A Produits)

Synonymes: anticorps myo5a, anticorps MGC53270, anticorps si:dkey-266j9.1, anticorps MYOA, anticorps MYO5A, anticorps D, anticorps Dop, anticorps Myh12, anticorps 9630007J19Rik, anticorps AI413174, anticorps AI661011, anticorps Dbv, anticorps MVa, anticorps Myo5, anticorps MyoVA, anticorps Sev-1, anticorps d, anticorps d-120J, anticorps flail, anticorps flr, anticorps DILUTE, anticorps myoxin), anticorps non-muscle, anticorps GS1, anticorps MYH12, anticorps MYO5, anticorps MYR12, anticorps myosin VA L homeolog, anticorps myosin VAa, anticorps myosin VA, anticorps myosin va, anticorps myo5a.L, anticorps myo5aa, anticorps MYO5A, anticorps PY04789, anticorps Myo5a

Sujet: 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.

ID gène: 4644

UniProt: Q9Y4I1

Pathways: Hormone Transport, Peptide Hormone Metabolism