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L2HGDH antibody (Middle Region)

The Rabbit Polyclonal anti-L2HGDH antibody has been validated for WB and EIA. It is suitable to detect L2HGDH in samples from Human and Mouse.
Catalog No. ABIN951995

Quick Overview for L2HGDH antibody (Middle Region) (ABIN951995)

Target

See all L2HGDH Antibodies
L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))

Reactivity

  • 26
  • 12
  • 6
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 32
Rabbit

Clonality

  • 32
Polyclonal

Conjugate

  • 19
  • 5
  • 3
  • 3
  • 1
  • 1
This L2HGDH antibody is un-conjugated

Application

  • 24
  • 21
  • 11
  • 1
Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 7
    • 6
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 139-167, Middle Region

    Specificity

    This antibody detects L2HGDH/ Duranin.

    Cross-Reactivity (Details)

    Species reactivity (tested):Human, Mouse

    Purification

    Purified through a protein A column; followed by peptide affinity purification.

    Immunogen

    Synthetic peptide - KLH conjugated - corresponding to the central region (between 139-167aa) of human L2HGDH/Duranin.

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target

    L2HGDH (L-2-Hydroxyglutarate Dehydrogenase (L2HGDH))

    Alternative Name

    Duranin

    Background

    The L2HGDH gene encodes L-2-hydroxyglutarate dehydrogenase, a FAD-dependent enzyme that oxidizes L-2-hydroxyglutarate to alpha-ketoglutarate in a variety of mammalian tissues. Mutations in this gene cause L-2-hydroxyglutaric aciduria, a rare autosomal recessive neurometabolic disorder resulting in moderate to severe mental retardation.Synonyms: C14orf160, L-2-hydroxyglutarate dehydrogenase, L2HGDH, hydroxyglutarate dehydrogenase

    Gene ID

    79944

    NCBI Accession

    NP_079160
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