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Hexosaminidase A (HEXA) (C-Term) Peptid

HEXA Reaktivität: Human Wirt: Synthetic BP, IHC, WB
Produktnummer ABIN977949

Kurzübersicht für Hexosaminidase A (HEXA) (C-Term) Peptid (ABIN977949)

Target

Hexosaminidase A (HEXA)

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

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

    C-Term

    Sequenz

    WKDFYIVEPL AFEGTPEQKA LVIGGEACMW GEYVDNTNLV PRLWPRAGAV

    Produktmerkmale

    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.

    Aufreinigung

    Purified
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    Hexosaminidase A (HEXA)

    Hintergrund

    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

    Molekulargewicht

    48 kDa

    Gen-ID

    3073

    NCBI Accession

    NM_000520, NP_000511

    UniProt

    P06865
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