GBA2 anticorps (AA 17-869)

N° du produit ABIN7871244

L’anticorps anti-GBA2 Polyclonal Lapin est utilisé pour la détection de GBA2 dans des échantillons de Humain, Souris et Rat. Il a été validé pour WB, ELISA et FACS.

Aperçu rapide pour GBA2 anticorps (AA 17-869) (ABIN7871244)

Antigène: GBA2 (Glucosidase, beta (Bile Acid) 2 (GBA2))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GBA2 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Détail du produit anti-GBA2 anticorps

Épitope: AA 17-869

Fonction: GBA2 Antibody / Non-lysosomal glucosylceramidase

Purification: Immunogen affinity purified

Immunogène: E.coli-derived human GBA2 recombinant protein (Position: E17-Q869) was used as the immunogen for the GBA2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the GBA2 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 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: After reconstitution, the GBA2 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 GBA2

Antigène: GBA2 (Glucosidase, beta (Bile Acid) 2 (GBA2))

Autre désignation: GBA2

Sujet: GBA2 antibody detects Non-lysosomal glucosylceramidase, a cytoplasmic enzyme responsible for the hydrolysis of glucosylceramide to glucose and ceramide outside of lysosomes. The UniProt recommended name is Non-lysosomal glucosylceramidase (GBA2). This enzyme participates in sphingolipid metabolism and maintains the balance of glycosphingolipids that influence membrane structure, signaling, and lipid homeostasis.

Functionally, GBA2 antibody identifies a 927-amino-acid membrane-associated protein localized to the endoplasmic reticulum and Golgi apparatus. GBA2 catalyzes the removal of glucose from glucosylceramide, complementing the lysosomal enzyme GBA1 but functioning in non-lysosomal compartments. By regulating ceramide and glucosylceramide levels, GBA2 affects cell differentiation, apoptosis, and neuronal lipid metabolism.

The GBA2 gene is located on chromosome 9p13.3 and is highly expressed in brain, liver, testis, and kidney. Its activity is essential for maintaining sphingolipid turnover and membrane lipid composition, particularly in neuronal and reproductive tissues. GBA2 functions as a key metabolic enzyme in glycosphingolipid homeostasis and intracellular lipid transport.

Pathologically, mutations in GBA2 cause hereditary spastic paraplegia type 46 and autosomal recessive cerebellar ataxia, disorders characterized by impaired motor function and cerebellar degeneration. Loss of GBA2 activity leads to accumulation of glucosylceramide, resulting in disrupted lipid trafficking and neuronal dysfunction. Research using GBA2 antibody supports studies in lipid metabolism, neurobiology, and metabolic disease mechanisms.

GBA2 antibody is validated for western blotting, immunohistochemistry, and immunofluorescence to detect glucosylceramidase enzymes. NSJ Bioreagents provides GBA2 antibody reagents optimized for studies in sphingolipid metabolism, cellular signaling, and neurological disorders.

Structurally, Non-lysosomal glucosylceramidase belongs to the glycoside hydrolase family 116 and contains a catalytic domain with a conserved nucleophilic residue required for glucosyl transfer. The enzyme is anchored to membranes through hydrophobic regions and operates in concert with lipid transporters. This antibody facilitates investigation of GBA2's role in non-lysosomal glycosphingolipid metabolism and neurological function.

UniProt: Q9HCG7