NAGLU anticorps (AA 24-489)

N° du produit ABIN8012995

Cet anticorps anti-NAGLU Polyclonal Lapin (ABIN8012995) détecte spécifiquement NAGLU dans WB et ELISA. L’anticorps est réactif avec des échantillons de Souris, Humain et Rat.

Aperçu rapide pour NAGLU anticorps (AA 24-489) (ABIN8012995)

Antigène: NAGLU (N-Acetylglucosaminidase, alpha (NAGLU))

Reactivité: Souris, Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NAGLU est non-conjugé

Application: Western Blotting (WB), ELISA

Classe de qualité: Carrier-free

Détail du produit anti-NAGLU anticorps

Épitope: AA 24-489

Fonction: Anti-NAGLU Antibody

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

Attributs du produit: Anti-NAGLU Antibody. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human NAGLU recombinant protein (Position: D24-D489).

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Stock: 4 °C,-20 °C

Stockage commentaire: At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur NAGLU

Antigène: NAGLU (N-Acetylglucosaminidase, alpha (NAGLU))

Autre désignation: NAGLU

Sujet:

Background: N-acetylglucosaminidase, alpha is a protein that in humans is encoded by the NAGLU gene. This gene encodes an enzyme that degrades heparan sulfate by hydrolysis of terminal N-acetyl-D-glucosamine residues in N-acetyl-alpha-D-glucosaminides. Defects in this gene are the cause of mucopolysaccharidosis type IIIB (MPS-IIIB), also known as Sanfilippo syndrome B. This disease is characterized by the lysosomal accumulation and urinary excretion of heparan sulfate.

Gene Full Name: N-acetyl-alpha-glucosaminidase

Poids moléculaire: 82 kDa

ID gène: 4669

UniProt: P54802

Pathways: Glycosaminoglycan Metabolic Process