MYO5A anticorps (AA 1784-1833)

N° du produit ABIN1451376

Cet anticorps anti-MYO5A Polyclonal Lapin (ABIN1451376) détecte spécifiquement MYO5A dans WB et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour MYO5A anticorps (AA 1784-1833) (ABIN1451376)

Antigène: MYO5A (Myosin VA (MYO5A))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MYO5A est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Détail du produit anti-MYO5A anticorps

Épitope: AA 1784-1833

Fonction: Myosin VA Antibody

Specificité: Myosin VA Polyclonal Antibody detects endogenous levels of Myosin VA protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: The antiserum was produced against synthesized peptide derived from human MYO5A. AA range:1784-1833

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000,IHC 1:50-300

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur MYO5A

Antigène: MYO5A (Myosin VA (MYO5A))

Autre désignation: MYO5A

Sujet:

Synonyms: MYO5A, MYH12, Unconventional myosin-Va, Dilute myosin heavy chain, non-muscle, Myosin heavy chain 12, Myosin-12, Myoxin

Background: 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, Dec 2008],

Gene Name: MYO5A

Protein Name: Unconventional myosin-Va

Poids moléculaire: 215 kDa

ID gène: 4644

OMIM: 160777

UniProt: Q9Y4I1

Pathways: Hormone Transport, Peptide Hormone Metabolism