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ALDH4A1 anticorps (AA 354-563)

L’anticorps Lapin Polyclonal anti-ALDH4A1 a été validé pour WB et IF. Il convient pour détecter ALDH4A1 dans des échantillons de Humain.
N° du produit ABIN3023403

Aperçu rapide pour ALDH4A1 anticorps (AA 354-563) (ABIN3023403)

Antigène

Voir toutes ALDH4A1 Anticorps
ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

Reactivité

  • 26
  • 11
  • 10
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 21
  • 5
Lapin

Clonalité

  • 24
  • 2
Polyclonal

Conjugué

  • 26
Cet anticorp ALDH4A1 est non-conjugé

Application

  • 26
  • 16
  • 9
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Épitope

    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 354-563

    Séquence

    LYVPHSLWPQ IKGRLLEEHS RIKVGDPAED FGTFFSAVID AKSFARIKKW LEHARSSPSL TILAGGKCDD SVGYFVEPCI VESKDPQEPI MKEEIFGPVL SVYVYPDDKY KETLQLVDST TSYGLTGAVF SQDKDVVQEA TKVLRNAAGN FYINDKSTGS IVGQQPFGGA RASGTNDKPG GPHYILRWTS PQVIKETHKP LGDWSYAYMQ

     Réactivité croisée

    Humain, Souris

    Attributs du produit

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    Recombinant fusion protein containing a sequence corresponding to amino acids 354-563 of human ALDH4A1 (NP_003739.2).

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

    Autre désignation

    ALDH4A1

    Sujet

    This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.,ALDH4A1,ALDH4,P5CD,P5CDh,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Amino acid metabolism,ALDH4A1

    Poids moléculaire

    55 kDa/56 kDa/61 kDa

    ID gène

    8659

    UniProt

    P30038

    Pathways

    Monocarboxylic Acid Catabolic Process
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