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DMGDH anticorps (C-Term)

Cet anticorps Lapin Polyclonal détecte spécifiquement DMGDH dans WB. Il présente une réactivité envers Humain, Rat, Porc et Cheval.
N° du produit ABIN2789894

Aperçu rapide pour DMGDH anticorps (C-Term) (ABIN2789894)

Antigène

Voir toutes DMGDH Anticorps
DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

Reactivité

  • 30
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Rat, Porc, Cheval

Hôte

  • 30
Lapin

Clonalité

  • 30
Polyclonal

Conjugué

  • 15
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DMGDH est non-conjugé

Application

  • 20
  • 17
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 8
    • 6
    • 6
    • 1
    • 1
    • 1
    • 1
    C-Term

    Séquence

    YVPVQLSEVG QQVEVELLGK NYPAVIIQEP LVLTEPTRNR LQKKGGKDKT

    Homologie

    Horse: 92%, Human: 100%, Pig: 100%, Rat: 93%

    Attributs du produit

    This is a rabbit polyclonal antibody against DMGDH. It was validated on Western Blot.

    Purification

    Affinity Purified
  • Indications d'application

    Optimal working dilutions should be determined experimentally by the investigator.

    Commentaires

    Antigen size: 866 AA

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    Lot specific

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Antigène

    DMGDH (Dimethylglycine Dehydrogenase (DMGDH))

    Autre désignation

    DMGDH

    Sujet

    This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum.
    Alias Symbols: DMGDHD, ME2GLYDH
    Protein Size: 866

    Poids moléculaire

    91 kDa

    ID gène

    29958

    NCBI Accession

    NM_013391, NP_037523

    UniProt

    Q9UI17
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