GLA anticorps

N° du produit ABIN7880847

L’anticorps anti-GLA Polyclonal Lapin est utilisé pour la détection de GLA dans des échantillons de Humain. Il a été validé pour WB et IHC (p).

Aperçu rapide pour GLA anticorps (ABIN7880847)

Antigène: GLA (Galactosidase, alpha (GLA))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GLA est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-GLA anticorps

Fonction: Galactosidase alpha Antibody / Gla

Séquence: KRKLGFYEWT SRLRSHIN

Purification: Affinity purified

Immunogène: Amino acids KRKLGFYEWTSRLRSHIN from the human protein were used as the immunogen for the Galactosidase alpha antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Galactosidase alpha antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Galactosidase alpha antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur GLA

Antigène: GLA (Galactosidase, alpha (GLA))

Autre désignation: Galactosidase alpha

Sujet: Alpha-galactosidase is a glycoside hydrolase enzyme that encoded by the GLA gene. This gene is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.

UniProt: P06280

Pathways: SARS-CoV-2 Protein Interactome