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ALDH6A1 anticorps (AA 1-195)

ALDH6A1 Reactivité: Humain WB, ELISA, IHC, FACS, ICC Hôte: Souris Monoclonal 6H9B8 unconjugated
N° du produit ABIN5542265
  • Antigène Voir toutes ALDH6A1 Anticorps
    ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))
    Épitope
    • 9
    • 8
    • 6
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-195
    Reactivité
    • 57
    • 9
    • 7
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain
    Hôte
    • 44
    • 10
    • 3
    Souris
    Clonalité
    • 49
    • 8
    Monoclonal
    Conjugué
    • 31
    • 5
    • 5
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp ALDH6A1 est non-conjugé
    Application
    • 45
    • 33
    • 29
    • 11
    • 9
    • 5
    • 5
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC)
    Fonction
    ALDH6A1 Antibody
    Purification
    Purified antibody
    Immunogène
    Purified recombinant fragment of human ALDH6A1 (AA: 1-195) expressed in E. Coli.
    Clone
    6H9B8
    Isotype
    IgG1
  • Indications d'application

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified antibody in PBS with 0.05 % sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Antigène
    ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))
    Autre désignation
    ALDH6A1 (ALDH6A1 Produits)
    Sujet

    Description: This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. Alternate splicing results in multiple transcript variants.

    Aliases: MMSDH, MMSADHA

    Poids moléculaire
    57.8kDa
    ID gène
    4329
    HGNC
    4329
    UniProt
    Q02252
    Pathways
    Brown Fat Cell Differentiation
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