NAGA antibody (AA 43-329)

Catalog No. ABIN7825572

This Rabbit Polyclonal antibody specifically detects NAGA in WB and ELISA. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for NAGA antibody (AA 43-329) (ABIN7825572)

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

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NAGA antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-NAGA Antibody

Binding Specificity: AA 43-329

Purpose: Anti-NAGA Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins

Characteristics: 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.

Immunogen: 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

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
ELISA, 0.1-0.5 μg/mL

Restrictions: For Research Use only

Handling

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.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for NAGA

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

Alternative Name: NAGA

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).

Molecular Weight: 60 kDa

Gene ID: 4668

UniProt: P17050