POMGNT1 anticorps (AA 96-394) (HRP)

N° du produit ABIN8027761

Cet anticorps anti-POMGNT1 Polyclonal Lapin conjugué à HRP (ABIN8027761) détecte spécifiquement POMGNT1 dans ELISA, WB et IHC. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour POMGNT1 anticorps (AA 96-394) (HRP) (ABIN8027761)

Antigène: POMGNT1 (Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp POMGNT1 est conjugé à/à la HRP

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

Détail du produit anti-POMGNT1 anticorps (HRP)

Épitope: AA 96-394

Fonction: Anti-POMGNT1 Antibody HRP Conjugated

Homologie: Human POMGNT1 shares 99.7% amino acid (aa) sequence identity with both mouse,rat POMGNT1.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human POMGNT1 recombinant protein (Position: R96-E394). Human POMGNT1 shares 99.7% amino acid (aa) sequence identity with both mouse and rat POMGNT1.

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, 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.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur POMGNT1

Antigène: POMGNT1 (Protein O-Linked Mannose Beta1,2-N-Acetylglucosaminyltransferase (POMGNT1))

Autre désignation: POMGNT1

Sujet:

Background: Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 is an enzyme that in humans is encoded by the POMGNT1 gene. This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.

Gene Full Name: protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)

ID gène: 55624

UniProt: Q8WZA1