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PGD antibody (AA 236-265)

This anti-PGD antibody is a Rabbit Polyclonal antibody detecting PGD in WB, FACS and IHC (p). Suitable for Human and Mouse.
Catalog No. ABIN651639

Quick Overview for PGD antibody (AA 236-265) (ABIN651639)

Target

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

Reactivity

  • 52
  • 13
  • 10
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
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Human, Mouse

Host

  • 47
  • 5
Rabbit

Clonality

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Polyclonal

Conjugate

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  • 4
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PGD antibody is un-conjugated

Application

  • 36
  • 23
  • 16
  • 16
  • 10
  • 10
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
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Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB22902
  • Binding Specificity

    • 12
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    AA 236-265

    Predicted Reactivity

    Pig, Rat, Sh

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This PGD antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 236-265 amino acids from the Central region of human PGD.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    PGD (Phosphogluconate Dehydrogenase (PGD))

    Alternative Name

    PGD

    Background

    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.

    Molecular Weight

    53140

    Gene ID

    5226

    NCBI Accession

    NP_002622

    UniProt

    P52209
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