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HADH anticorps (AA 57-314)

Cet anticorps anti-HADH est un anticorps Poulet Polyclonal détectant HADH dans WB. Adapté pour Humain, Souris et Rat.
N° du produit ABIN2468091

Aperçu rapide pour HADH anticorps (AA 57-314) (ABIN2468091)

Antigène

Voir toutes HADH Anticorps
HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Reactivité

  • 39
  • 36
  • 22
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Humain, Souris, Rat

Hôte

  • 40
  • 14
  • 1
Poulet

Clonalité

  • 42
  • 13
Polyclonal

Conjugué

  • 26
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp HADH est non-conjugé

Application

  • 40
  • 15
  • 14
  • 13
  • 13
  • 10
  • 9
  • 9
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 57-314

    Purification

    Immunoaffinity Purified
  • Indications d'application

    Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial antibody can be used for the detection of Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial by Western Blot.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline. No preservatives added.

    Agent conservateur

    Without preservative

    Conseil sur la manipulation

    As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    HADHSC antibody can be stored at 4 °C for short term (weeks). Long term storage should be at -20 °C.
  • Antigène

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    Autre désignation

    HADHSC

    Sujet

    FUNCTION: Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts it highest activity toward 3-hydroxybutyryl-CoA.

    DISEASE: Defects in HADHSC are the cause of 3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HAD deficiency) [MIM:609609]. HAD deficiency is a metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.

    Poids moléculaire

    34.3 kDa (calculated)

    ID gène

    3033

    NCBI Accession

    NP_005318

    UniProt

    Q16836

    Pathways

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
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