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ACADL antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects ACADL in WB. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN657058

Quick Overview for ACADL antibody (N-Term) (ABIN657058)

Target

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

Reactivity

  • 60
  • 24
  • 4
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 67
  • 1
Rabbit

Clonality

  • 68
Polyclonal

Conjugate

  • 26
  • 6
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
This ACADL antibody is un-conjugated

Application

  • 49
  • 31
  • 26
  • 26
  • 13
  • 8
  • 6
  • 6
  • 5
Western Blotting (WB)

Clone

RB32459
  • Binding Specificity

    • 15
    • 15
    • 8
    • 7
    • 7
    • 4
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-43, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This ACADL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 14-43 amino acids from the N-terminal region of human ACADL.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in 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.

    Storage

    4 °C,-20 °C

    Expiry Date

    6 months
  • Target

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

    Alternative Name

    ACADL

    Background

    The protein encoded by this gene 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

    47656

    NCBI Accession

    NP_001599

    UniProt

    P28330

    Pathways

    Monocarboxylic Acid Catabolic Process
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