Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

GBA antibody

The Rabbit Polyclonal anti-GBA antibody (ABIN1387836) specifically detects GBA in WB, IHC (p) and IF (p). The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN1387836
$384.62
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 8 to 11 Business Days

Quick Overview for GBA antibody (ABIN1387836)

Target

See all GBA Antibodies
GBA (Glucosidase, Beta, Acid (GBA))

Reactivity

  • 82
  • 43
  • 40
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 91
  • 13
Rabbit

Clonality

  • 73
  • 31
Polyclonal

Conjugate

  • 39
  • 17
  • 11
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GBA antibody is un-conjugated

Application

  • 72
  • 38
  • 23
  • 13
  • 10
  • 10
  • 10
  • 9
  • 8
  • 5
  • 5
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human Acid beta-glucosidase

    Isotype

    IgG
  • Application Notes

    WB 1:100-1000
    IHC-P 1:100-500
    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    Store at -20°C

    Expiry Date

    12 months
  • Target

    GBA (Glucosidase, Beta, Acid (GBA))

    Alternative Name

    GBA/Acid beta-Glucosidase

    Background

    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
You are here:
Chat with us!