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Hexosaminidase A antibody (AA 89-529)

This Mouse Monoclonal antibody specifically detects Hexosaminidase A in WB, ELISA and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN5775909

Quick Overview for Hexosaminidase A antibody (AA 89-529) (ABIN5775909)

Target

See all Hexosaminidase A (HEXA) Antibodies
Hexosaminidase A (HEXA)

Reactivity

  • 59
  • 25
  • 15
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 48
  • 15
Mouse

Clonality

  • 50
  • 13
Monoclonal

Conjugate

  • 42
  • 4
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Hexosaminidase A antibody is un-conjugated

Application

  • 52
  • 32
  • 15
  • 8
  • 7
  • 5
  • 4
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Clone

AT20F1
  • Binding Specificity

    • 8
    • 8
    • 8
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 89-529

    Immunogen

    Recombinant human HEXA (89-529aa) purified from E. coli

    Isotype

    IgG2a lambda
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Storage

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
  • Target

    Hexosaminidase A (HEXA)

    Alternative Name

    Hexosaminidase A/HEXA

    Background

    HEXA (Hexosaminidase A), also designated beta-Hexosaminidase A, is responsible for the degradation of GM2 gangliosides, and a variety of other molecules containing terminal N-acetyl hexosamines, in the brain and other tissues. A mutation in the a subunit of hexosaminidase is the cause of Tay-Sachs disease (TSD), also known as GM2-gangliosidosis type I. TSD is a fatal autosomal recessive lysosomal storage disease of the central nervous system (CNS) caused by insufficient activity of the HEXA enzyme that results in a failure to process GM2 gangliosides. The accumulation of GM2 ganglioside in the absence of HEXA activity causes progressive destruction of the CNS.

    NCBI Accession

    NP_000511

    Pathways

    Sensory Perception of Sound, Glycosaminoglycan Metabolic Process
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