Anti-GBA antibody

Anti-GBA antibody

Catalog Number:
A001017471STJ
Mfr. No.:
STJ110718
Price:
$297
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      • Overview
        • This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.

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      • Properties
        • Host
          rabbit
          Antibody Type
          polyclonal
          Isotype
          IgG
          Reactivity
          human
          Immunogen
          Recombinant fusion protein containing a sequence corresponding to amino acids 40-250 of human GBA (NP_000148. 2).
          Purification
          Affinity purification
          Conjugate
          Unconjugated
          Formulation
          PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
          Storage
          Store at -20°C and avoid freeze-thaw cycles.
          Regulatory Status
          RUO
          Antigen
          Lysosomal Acid Glucosylceramidase; Lysosomal Acid Gcase; Acid Beta-Glucosidase; Alglucerase; Beta-Glucocerebrosidase; Beta-Gc; Cholesterol Glucosyltransferase; Sgtase; Cholesteryl-Beta-Glucosidase; D-Glucosyl-N-Acylsphingosine Glucohydrolase; Imiglucerase (Gene ID:2629; UniProt:P04062)

          * For research use only

      • Applications
        • Application
          WB
        • Application Dilutions
          WB 1:500-1:2000

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