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MDH1 anticorps

Cet anticorps anti-MDH1 est un anticorps Lapin Monoclonal détectant MDH1 dans WB. Adapté pour Humain.
N° du produit ABIN7268379

Aperçu rapide pour MDH1 anticorps (ABIN7268379)

Antigène

Voir toutes MDH1 Anticorps
MDH1 (Malate Dehydrogenase 1, NAD (Soluble) (MDH1))

Reactivité

  • 78
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Humain

Hôte

  • 56
  • 26
  • 4
  • 1
Lapin

Clonalité

  • 60
  • 26
Monoclonal

Conjugué

  • 48
  • 6
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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Cet anticorp MDH1 est non-conjugé

Application

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Western Blotting (WB)
  • Fonction

    MDH1 Rabbit mAb

     Réactivité croisée

    Humain, Souris, Rat

    Attributs du produit

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogène

    A synthesized peptide derived from human MDH1

    Isotype

    IgG
  • Indications d'application

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,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

    MDH1 (Malate Dehydrogenase 1, NAD (Soluble) (MDH1))

    Autre désignation

    MDH1

    Sujet

    This gene encodes an enzyme that catalyzes the NAD/NADH-dependent, reversible oxidation of malate to oxaloacetate in many metabolic pathways, including the citric acid cycle. Two main isozymes are known to exist in eukaryotic cells: one is found in the mitochondrial matrix and the other in the cytoplasm. This gene encodes the cytosolic isozyme, which plays a key role in the malate-aspartate shuttle that allows malate to pass through the mitochondrial membrane to be transformed into oxaloacetate for further cellular processes. Alternatively spliced transcript variants have been found for this gene. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Pseudogenes have been identified on chromosomes X and 6. [provided by RefSeq, Feb 2016],HEL-S-32, MDH-s, MDHA, MGC:1375, MOR2,Cancer,Carbohydrate metabolism,Endocrine & Metabolism,Signal Transduction,MDH1

    Poids moléculaire

    36kDa

    ID gène

    4190

    UniProt

    P40925
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