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Hexosaminidase A (HEXA) (C-Term) Peptide

HEXA Reactivity: Human Host: Synthetic BP, IHC, WB
Catalog No. ABIN977949

Quick Overview for Hexosaminidase A (HEXA) (C-Term) Peptide (ABIN977949)

Target

Hexosaminidase A (HEXA)

Origin

Human

Source

  • 2
Synthetic

Application

Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
  • Protein Region

    C-Term

    Sequence

    WKDFYIVEPL AFEGTPEQKA LVIGGEACMW GEYVDNTNLV PRLWPRAGAV

    Characteristics

    This is a synthetic peptide designed for use in combination with anti-HEXA Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    Hexosaminidase A (HEXA)

    Background

    This gene encodes the alpha subunit of the lysosomal enzyme beta-hexosaminidase that, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Beta-hexosaminidase is composed of two subunits, alpha and beta, which are encoded by separate genes. Both beta-hexosaminidase alpha and beta subunits are members of family 20 of glycosyl hydrolases. Mutations in the alpha or beta subunit genes lead to an accumulation of GM2 ganglioside in neurons and neurodegenerative disorders termed the GM2 gangliosidoses. Alpha subunit gene mutations lead to Tay-Sachs disease (GM2-gangliosidosis type I).

    Alias Symbols: MGC99608, TSD

    Protein Interaction Partner: GM2A,GM2A,USP22

    Protein Size: 529

    Molecular Weight

    48 kDa

    Gene ID

    3073

    NCBI Accession

    NM_000520, NP_000511

    UniProt

    P06865
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