NAGA anticorps (AA 43-329)

N° du produit ABIN7825572

Cet anticorps Lapin Polyclonal détecte spécifiquement NAGA dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain, Rat et Souris.

Aperçu rapide pour NAGA anticorps (AA 43-329) (ABIN7825572)

Antigène: NAGA (N-Acetylgalactosaminidase, alpha (NAGA))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NAGA est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-NAGA anticorps

Épitope: AA 43-329

Fonction: Anti-NAGA Antibody

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

Homologie: Human NAGAshares 86.7%,85.4% amino acid (aa) sequence identity with mouse,rat NAGA,respectively.

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

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human NAGA recombinant protein (Position: D43-R329). Human NAGAshares 86.7% and 85.4% amino acid (aa) sequence identity with mouse and rat NAGA, respectively.

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 NAGA

Antigène: NAGA (N-Acetylgalactosaminidase, alpha (NAGA))

Autre désignation: NAGA

Sujet:

Background: NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of Schindler disease types I and II (type II also known as Kanzaki disease).

Gene Full Name: alpha-N-acetylgalactosaminidase

Poids moléculaire: 60 kDa

ID gène: 4668

UniProt: P17050