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ACAT1 antibody

This Rabbit Polyclonal antibody specifically detects ACAT1 in WB. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN631042

Quick Overview for ACAT1 antibody (ABIN631042)

Target

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

Reactivity

  • 68
  • 35
  • 29
  • 4
  • 4
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 61
  • 5
  • 4
Rabbit

Clonality

  • 60
  • 10
Polyclonal

Conjugate

  • 43
  • 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
  • 26
  • 13
  • 13
  • 11
  • 9
  • 8
  • 7
  • 3
  • 3
  • 2
Western Blotting (WB)
  • Purification

    Affinity purified

    Immunogen

    ACAT1 antibody was raised using a synthetic peptide corresponding to a region with amino acids SYTRSKAAWEAGKFGNEVIPVTVTVKGQPDVVVKEDEEYKRVDFSKVPKL
  • Application Notes

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Comment

    ACAT1 Blocking Peptide, (ABIN5611882), is also available for use as a blocking control in assays to test for specificity of this ACAT1 antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ACAT1 antibody in PBS

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

    Alternative Name

    ACAT1

    Background

    ACAT1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. The gene encoding ACAT1 spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene 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.

    Molecular Weight

    41 kDa (MW of target protein)
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