POMT1 anticorps (AA 224-747) (Fluoro550)

N° du produit ABIN8028585

L’anticorps anti-POMT1 Polyclonal Lapin est utilisé pour la détection de POMT1 dans des échantillons de Humain et Rat. Il a été validé pour FACS.

Aperçu rapide pour POMT1 anticorps (AA 224-747) (Fluoro550) (ABIN8028585)

Antigène: POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POMT1 est conjugé à/à la Fluoro550

Application: Flow Cytometry (FACS)

Détail du produit anti-POMT1 anticorps (Fluoro550)

Épitope: AA 224-747

Fonction: Anti-POMT1 Antibody Fluoro550 Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human POMT1 shares 81.1%,80.9% amino acid (aa) sequence identity with mouse,rat POMT1,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human POMT1 recombinant protein (Position: H224-H747). Human POMT1 shares 81.1% and 80.9% amino acid (aa) sequence identity with mouse and rat POMT1, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur POMT1

Antigène: POMT1 (Protein-O-Mannosyltransferase 1 (POMT1))

Autre désignation: POMT1

Sujet:

Background: Protein O-mannosyl-transferase 1 is an enzyme that in humans is encoded by the POMT1 gene. The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene.

Gene Full Name: protein O-mannosyltransferase 1

ID gène: 10585

UniProt: Q9Y6A1