DPAGT1 anticorps (N-Term)

N° du produit ABIN657891

Cet anticorps anti-DPAGT1 Polyclonal Lapin (Clone RB32141) (ABIN657891) détecte spécifiquement DPAGT1 dans WB. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour DPAGT1 anticorps (N-Term) (ABIN657891)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DPAGT1 est non-conjugé

Application: Western Blotting (WB)

Clone: RB32141

Détail du produit anti-DPAGT1 anticorps

Épitope: AA 28-57, N-Term

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 28-57 amino acids from the N-terminal region of human DPAGT1.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. 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: DPAGT1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Date de péremption: 6 months

Détails sur DPAGT1

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

Autre désignation: DPAGT1

Sujet: The protein 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