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Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1) (C-Term) Peptid

ALDH7A1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN5514366
150,78 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 15 bis 22 Werktagen

Kurzübersicht für Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1) (C-Term) Peptid (ABIN5514366)

Target

ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

Spezies

Human

Quelle

  • 2
Synthetic

Applikation

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

    C-Term

    Sequenz

    LGRIFRWLGP KGSDCGIVNV NIPTSGAEIG GAFGGEKHTG GGRESGSDAW

    Produktmerkmale

    This is a synthetic peptide designed for use in combination with anti- ALDH7A1 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.
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    ALDH7A1 (Aldehyde Dehydrogenase 7 Family, Member A1 (ALDH7A1))

    Hintergrund

    The protein encoded by this gene is a member of subfamily 7 in the aldehyde dehydrogenase gene family. These enzymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This particular member has homology to a previously described protein from the green garden pea, the 26g pea turgor protein. It is also involved in lysine catabolism that is known to occur in the mitochondrial matrix. Recent reports show that this protein is found both in the cytosol and the mitochondria, and the two forms likely arise from the use of alternative translation initiation sites. An additional variant encoding a different isoform has also been found for this gene. Mutations in this gene are associated with pyridoxine-dependent epilepsy. Several related pseudogenes have also been identified.

    Alias Symbols: EPD, PDE, ATQ1

    Protein Size: 475

    Gen-ID

    501

    NCBI Accession

    NM_001182, NP_001173
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