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ALDOA anticorps

L’anticorps Lapin Polyclonal anti-ALDOA a été validé pour WB, ELISA et IHC. Il convient pour détecter ALDOA dans des échantillons de Humain, Souris et Rat.
N° du produit ABIN7236790

Aperçu rapide pour ALDOA anticorps (ABIN7236790)

Antigène

Voir toutes ALDOA Anticorps
ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

Reactivité

  • 80
  • 31
  • 29
  • 17
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 59
  • 14
  • 12
  • 2
Lapin

Clonalité

  • 70
  • 16
Polyclonal

Conjugué

  • 58
  • 7
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
Cet anticorp ALDOA est non-conjugé

Application

  • 69
  • 40
  • 25
  • 22
  • 19
  • 13
  • 9
  • 7
  • 7
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human ALDOA

    Isotype

    IgG
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.3 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))

    Autre désignation

    ALDOA

    Sujet

    The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.

    Poids moléculaire

    39 kDa

    UniProt

    P04075

    Pathways

    Ribonucleoside Biosynthetic Process
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