DPAGT1 anticorps (AA 286-315)

N° du produit ABIN2843159

Cité dans 1 publication. Cet anticorps anti-DPAGT1 Polyclonal Lapin (Clone RB23874) (ABIN2843159) détecte spécifiquement DPAGT1 dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour DPAGT1 anticorps (AA 286-315) (ABIN2843159)

Antigène: DPAGT1 (Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DPAGT1 est non-conjugé

Application: Western Blotting (WB)

Clone: RB23874

Détail du produit anti-DPAGT1 anticorps

Épitope: AA 286-315

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This DPAGT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 286-315 amino acids from the Central region of human DPAGT1.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Références pour anticorps anti-DPAGT1 (ABIN2843159)

Klein, Robb, Rushing, Liu, Belaya, Beeson: "Congenital myasthenic syndrome caused by mutations in DPAGT." dans: Neuromuscular disorders : NMD, Vol. 25, Issue 3, pp. 253-6, (2015) (PubMed).

Détails sur DPAGT1

Antigène: DPAGT1 (Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1))

Autre désignation: DPAGT1

Sujet: DPAGT1 encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme.

Poids moléculaire: 46090

ID gène: 1798

NCBI Accession: NP_001373

UniProt: Q9H3H5