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PGD antibody (AA 200-250)

This anti-PGD antibody is a Rabbit Polyclonal antibody detecting PGD in WB and IP. Suitable for Human.
Catalog No. ABIN7450560

Quick Overview for PGD antibody (AA 200-250) (ABIN7450560)

Target

See all PGD Antibodies
PGD (Phosphogluconate Dehydrogenase (PGD))

Reactivity

  • 52
  • 14
  • 10
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 48
  • 4
Rabbit

Clonality

  • 46
  • 6
Polyclonal

Conjugate

  • 29
  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PGD antibody is un-conjugated

Application

  • 36
  • 23
  • 16
  • 15
  • 11
  • 9
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 11
    • 6
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 200-250

    Purpose

    Rabbit anti-PGD Antibody, Affinity Purified

    Predicted Reactivity

    Rat

    Purification

    Affinity Purified

    Immunogen

    Between AA 200 and 250

    Isotype

    IgG
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

    PGD (Phosphogluconate Dehydrogenase (PGD))

    Alternative Name

    PGD

    Background

    Background: 6-phosphogluconate dehydrogenase (PGD) 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[taken from NCBI Entrez Gene (Gene ID: 5226)].

    Gene ID

    5226

    UniProt

    P52209
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