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APRT anticorps (AA 5-49)

Cet anticorps anti-APRT est un anticorps Lapin Polyclonal détectant APRT dans WB et FACS. Adapté pour Humain.
N° du produit ABIN5647397

Aperçu rapide pour APRT anticorps (AA 5-49) (ABIN5647397)

Antigène

Voir toutes APRT Anticorps
APRT (Adenine Phosphoribosyltransferase (APRT))

Reactivité

  • 50
  • 6
  • 3
  • 2
  • 1
  • 1
Humain

Hôte

  • 46
  • 4
Lapin

Clonalité

  • 48
  • 2
Polyclonal

Conjugué

  • 29
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp APRT est non-conjugé

Application

  • 37
  • 21
  • 18
  • 10
  • 8
  • 7
  • 6
  • 5
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)
  • Épitope

    • 13
    • 8
    • 7
    • 6
    • 3
    • 1
    • 1
    • 1
    • 1
    AA 5-49

    Purification

    Antigen affinity purified

    Immunogène

    Amino acids 5-49 (ELQLVEQRIRSFPDFPTPGVVFRDISPVLKDPASFRAAIGLLARH-human) were used as the immunogen for the APRT antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the APRT antibody should be determined by the researcher.\. Western blot: 0.5-1 μg/mL,FACS: 1-3 μg/10^6 cells

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    -20 °C

    Stockage commentaire

    After reconstitution, the APRT antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Antigène

    APRT (Adenine Phosphoribosyltransferase (APRT))

    Autre désignation

    APRT

    Sujet

    Adenine phosphoribosyltransferase (APRTase) is an enzyme encoded by the APRT gene, found in humans on chromosome 16. It belongs to the purine/pyrimidine phosphoribosyltransferase family. A conserved feature of this gene is the distribution of CpG dinucleotides. This enzyme catalyzes the formation of AMP and inorganic pyrophosphate from adenine and 5-phosphoribosyl-1-pyrophosphate (PRPP). It also produces adenine as a by-product of the polyamine biosynthesis pathway. A homozygous deficiency in this enzyme causes 2,8-dihydroxyadenine urolithiasis. Two transcript variants encoding different isoforms have been found for this gene.

    UniProt

    P07741

    Pathways

    Ribonucleoside Biosynthetic Process
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