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Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1) Peptide

ALDH3A1 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN937432

Aperçu rapide pour Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1) Peptide (ABIN937432)

Antigène

ALDH3A1 (Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1))

Origine

Mammifères

Source

  • 7
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    DLHKNEWNAY YEEVVYVLEE IEYMIQKLPE WAADEPVEKT PQTQQDELYI

    Attributs du produit

    A synthetic peptide for use as a blocking control in assays to test for specificity of ALDH3 A1 antibody,
    Alternative Names: ALDH3A1 control peptide, ALDH3A1 antibody Blocking Peptide, Anti-ALDH3A1 Blocking Peptide, aldehyde dehydrogenase 3 family, memberA1 Blocking Peptide, ALDH3 Blocking Peptide, ALDHIII Blocking Peptide, MGC10406 Blocking Peptide, ALDH3A1, ALDHA1-3, ALDHA1 3, ALDHA1-3 Blocking Peptide, ALDHA1 3 Blocking Peptide
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    ALDH3A1 (Aldehyde Dehydrogenase 3 Family, Member A1 (ALDH3A1))

    Sujet

    Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified.

    Poids moléculaire

    50 kDa
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