NAGA anticorps (AA 43-329)

N° du produit ABIN7825572

Cet anticorps Lapin Polyclonal détecte spécifiquement NAGA dans WB et ELISA. Il présente une réactivité envers 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

Attributs du produit: Anti-NAGA Antibody catalog # A04163-1. Tested in WB, ELISA applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

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.

Détails sur NAGA

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

Autre désignation: NAGA

Sujet: 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).

Poids moléculaire: 60 kDa

ID gène: 4668

UniProt: P17050