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GALT antibody (AA 1-379)

The Rabbit Polyclonal anti-GALT antibody has been validated for WB, ELISA, IHC, IP and IF. It is suitable to detect GALT in samples from Human.
Catalog No. ABIN7153422

Quick Overview for GALT antibody (AA 1-379) (ABIN7153422)

Target

See all GALT Antibodies
GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

Reactivity

  • 47
  • 19
  • 13
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 46
  • 7
Rabbit

Clonality

  • 43
  • 10
Polyclonal

Conjugate

  • 30
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This GALT antibody is un-conjugated

Application

  • 35
  • 18
  • 11
  • 9
  • 6
  • 6
  • 5
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunoprecipitation (IP), Immunofluorescence (IF)
  • Binding Specificity

    • 12
    • 8
    • 6
    • 1
    • 1
    • 1
    AA 1-379

    Cross-Reactivity

    Human, Mouse, Rat

    Purification

    >95%, Protein G purified

    Immunogen

    Recombinant Human Galactose-1-phosphate uridylyltransferase protein (1-379AA)

    Isotype

    IgG
  • Application Notes

    Recommended dilution: WB:1:500-1:5000, IHC:1:20-1:200, IF:1:50-1:200, IP:1:200-1:2000,

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

    Preservative

    ProClin

    Precaution of Use

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

    Storage

    -20 °C,-80 °C

    Storage Comment

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target

    GALT (Galactose-1-Phosphate Uridylyltransferase (GALT))

    Alternative Name

    GALT

    Background

    Background: Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined.

    Aliases: Gal 1 P uridylyltransferase antibody, Gal-1-P uridylyltransferase antibody, Galactose 1 phosphate uridyl transferase antibody, Galactose 1 phosphate uridylyltransferase antibody, Galactose-1-phosphate uridylyltransferase antibody, GALT antibody, GALT_HUMAN antibody, UDP glucose hexose 1 phosphate uridylyltransferase antibody, UDP-glucose--hexose-1-phosphate uridylyltransferase antibody

    UniProt

    P07902
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