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GBA anticorps (AbBy Fluor® 488)

Cet anticorps Lapin Polyclonal détecte spécifiquement GBA dans IF (p). Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN1393270

Aperçu rapide pour GBA anticorps (AbBy Fluor® 488) (ABIN1393270)

Antigène

Voir toutes GBA Anticorps
GBA (Glucosidase, Beta, Acid (GBA))

Reactivité

  • 71
  • 41
  • 29
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 78
  • 15
Lapin

Clonalité

  • 72
  • 21
Polyclonal

Conjugué

  • 37
  • 17
  • 11
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp GBA est conjugé à/à la AbBy Fluor® 488

Application

  • 63
  • 30
  • 23
  • 15
  • 11
  • 10
  • 10
  • 9
  • 5
  • 4
  • 2
  • 1
Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Purification

    Purified by Protein A.

    Immunogène

    KLH conjugated synthetic peptide derived from human Acid beta-glucosidase

    Isotype

    IgG
  • Indications d'application

    IF(IHC-P)(1:50-200)

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 100 μg/mL BSA, 50 % glycerol and 0.09 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at 4°C

    Date de péremption

    12 months
  • Antigène

    GBA (Glucosidase, Beta, Acid (GBA))

    Autre désignation

    GBA/Acid beta-Glucosidase

    Sujet

    Beta-Glucosidase is a predominantly liver enzyme which efficiently hydrolyzes Beta-D-glucoside and Beta-D-galactoside. Defects in Beta-Glucosidase cause Gaucher disease, an inherited condition distinguished by the accumulation of glucosylceramide within the cells of the reticuloendothelial system. Beta-Glucosidase is used in enzyme replacement treatment aimed at treating Gaucher disease. The absorption of dietary flavonoid glycosides in humans involves a critical deglycosylation step that is mediated by epithelial Beta-glucosidases.


    Synonyms: Acid beta glucosidase, Acid beta-glucosidase, Alglucerase, Beta glucocerebrosidase, BETA GLUCOSIDASE, ACID, Beta-glucocerebrosidase, betaGC, D glucosyl N acylsphingosine glucohydrolase, D-glucosyl-N-acylsphingosine glucohydrolase, EC 3.2.1.45 , GBA, Gba protein, GBA1, GC antibody GCase, GCB, GLCM_HUMAN, GLUC, Glucocerebrosidase alt., Glucocerebrosidase, GLUCOCEREBROSIDASE PSEUDOGENE, Glucosidase beta, Glucosidase, beta, acid, Glucosidase, beta, acid includes glucosylceramidase, Glucosylceramidase, Imiglucerase, Lysosomal glucocerebrosidase.

    Pathways

    Cellular Glucan Metabolic Process
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