MUTYH anticorps (AA 1801-1939) (PE)

N° du produit ABIN6944193

Cet anticorps Lapin Polyclonal détecte spécifiquement MUTYH dans FACS. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour MUTYH anticorps (AA 1801-1939) (PE) (ABIN6944193)

Antigène: MUTYH (MutY Homolog (E. Coli) (MUTYH))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MUTYH est conjugé à/à la PE

Application: Flow Cytometry (FACS)

Détail du produit anti-MUTYH anticorps (PE)

Épitope: AA 1801-1939

Réactivité croisée: Humain, Souris

Homologie: Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human MYH 6

Isotype: IgG

Information d'application

Indications d'application: FCM 1:20-100

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur MUTYH

Antigène: MUTYH (MutY Homolog (E. Coli) (MUTYH))

Autre désignation: MYH

Sujet:

Synonyms: Alpha MHC, ASD3, CMD1S, CMH1, MGC138376, MGC138378, MPD1, MYH 6, MYH 7, MYH6, MYH7, MYHC A, MYHC, MYHC B, MyHC-alpha, MyHC-beta, MYHCA, MYHCB, Myosin heavy chain cardiac muscle alpha isoform, Myosin heavy chain cardiac muscle beta isoform, Myosin heavy polypeptide 7 cardiac muscle beta, MYH6_HUMAN, MYH7_HUMAN.

Background: Cardiac muscle myosin is a hexamer consisting of two heavy chain subunits, two light chain subunits, and two regulatory subunits. This gene encodes the alpha heavy chain subunit of cardiac myosin. The gene is located 4kb downstream of the gene encoding the beta heavy chain subunit of cardiac myosin. Mutations in this gene cause familial hypertrophic cardiomyopathy and atrial septal defect 3.

ID gène: 4625

Pathways: Réparation de l'ADN