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ACADL antibody (Middle Region)

This anti-ACADL antibody is a Rabbit Polyclonal antibody detecting ACADL in WB. Suitable for Human and Mouse.
Catalog No. ABIN631083

Quick Overview for ACADL antibody (Middle Region) (ABIN631083)

Target

See all ACADL Antibodies
ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reactivity

  • 61
  • 25
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse

Host

  • 68
  • 1
Rabbit

Clonality

  • 69
Polyclonal

Conjugate

  • 27
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This ACADL antibody is un-conjugated

Application

  • 50
  • 31
  • 26
  • 26
  • 13
  • 8
  • 6
  • 6
  • 5
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 15
    • 8
    • 8
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region

    Specificity

    ACADL antibody was raised against the middle region of ACADL

    Purification

    Affinity purified

    Immunogen

    ACADL antibody was raised using the middle region of ACADL corresponding to a region with amino acids LPQERLLIADVAISASEFMFEETRNYVKQRKAFGKTVAHLQTVQHKLAEL
  • Application Notes

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

    Comment

    ACADL Blocking Peptide, (ABIN5611873), is also available for use as a blocking control in assays to test for specificity of this ACADL antibody

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

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

    Concentration

    Lot specific

    Buffer

    PBS

    Handling Advice

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    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

    ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

    Alternative Name

    ACADL

    Background

    ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

    Molecular Weight

    44 kDa (MW of target protein)

    Pathways

    Monocarboxylic Acid Catabolic Process
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