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ACAT1 antibody (AA 296-329)

The Rabbit Polyclonal anti-ACAT1 antibody has been validated for WB, IHC and ELISA. It is suitable to detect ACAT1 in samples from Human and Mouse.
Catalog No. ABIN5647681

Quick Overview for ACAT1 antibody (AA 296-329) (ABIN5647681)

Target

See all ACAT1 Antibodies
ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

Reactivity

  • 67
  • 35
  • 28
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse

Host

  • 62
  • 5
  • 4
Rabbit

Clonality

  • 61
  • 10
Polyclonal

Conjugate

  • 44
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACAT1 antibody is un-conjugated

Application

  • 41
  • 28
  • 28
  • 13
  • 13
  • 12
  • 10
  • 9
  • 8
  • 3
  • 3
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Binding Specificity

    • 15
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 296-329

    Cross-Reactivity (Details)

    Expected species reactivity: Primate

    Purification

    Purified

    Immunogen

    A portion of amino acids 296-329 from the human protein was used as the immunogen for this ACAT1 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Western blot: 1:1000,IHC (Paraffin): 1:10-1:50

    Restrictions

    For Research Use only
  • Buffer

    In 1X PBS, pH 7.4, with 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

    -20 °C

    Storage Comment

    Aliquot the ACAT1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

    Alternative Name

    ACAT1

    Background

    Acetyl-CoA acetyltransferase 1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in the gene encoding ACAT1 are associated with the alpha-methylacetoaceticaciduria disorder,an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.

    UniProt

    P24752
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