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PGD anticorps (AA 1-171)

Cet anticorps anti-PGD est un anticorps Lapin Polyclonal détectant PGD dans WB et IF. Adapté pour Humain.
N° du produit ABIN1885683

Aperçu rapide pour PGD anticorps (AA 1-171) (ABIN1885683)

Antigène

Voir toutes PGD Anticorps
PGD (Phosphogluconate Dehydrogenase (PGD))

Reactivité

  • 51
  • 13
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Humain

Hôte

  • 46
  • 5
Lapin

Clonalité

  • 44
  • 7
Polyclonal

Conjugué

  • 28
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PGD est non-conjugé

Application

  • 35
  • 22
  • 16
  • 15
  • 11
  • 10
  • 4
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • Épitope

    • 12
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-171

    Purification

    Purified by antigen-affinity chromatography.

    Immunogène

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 171 of Human PGD
  • Indications d'application

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Agent conservateur

    Thimerosal (Merthiolate)

    Précaution d'utilisation

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Stock

    4 °C/-20 °C

    Stockage commentaire

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène

    PGD (Phosphogluconate Dehydrogenase (PGD))

    Autre désignation

    PGD

    Sujet

    6-phosphogluconate dehydrogenase is the second dehydrogenase in the pentose phosphate shunt.Deficiency of this enzyme is generally asymptomatic, and the inheritance of this disorder is autosomal dominant.Hemolysis results from combined deficiency of 6-phosphogluconate dehydrogenase and 6-phosphogluconolactonase suggesting a synergism of the two enzymopathies.[provided by RefSeq]

    Poids moléculaire

    53 kDa

    ID gène

    5226

    NCBI Accession

    NM_002631, NP_002622
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