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ACADL antibody (AA 31-210)

This Rabbit Polyclonal antibody specifically detects ACADL in WB and IHC. It exhibits reactivity toward Human.
Catalog No. ABIN1678519

Quick Overview for ACADL antibody (AA 31-210) (ABIN1678519)

Target

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

Reactivity

  • 60
  • 25
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human

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
  • 12
  • 8
  • 6
  • 6
  • 5
Western Blotting (WB), Immunohistochemistry (IHC)
  • Binding Specificity

    • 15
    • 15
    • 8
    • 8
    • 7
    • 5
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 31-210

    Sequence

    GGEERLETPS AKKLTDIGIR RIFSPEHDIF RKSVRKFFQE EVIPHHSEWE KAGEVSREVW EKAGKQGLLG VNIAEHLGGI GGDLYSAAIV WEEQAYSNCS GPGFSIHSGI VMSYITNHGS EEQIKHFIPQ MTAGKCIGAI AMTEPGAGSD LQGIKTNAKK DGSDWILNGS KVFISNGSLS

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 31-210 of human ACADL (NP_001599.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 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.,ACADL,ACAD4,LCAD,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Lipid Metabolism,Cardiovascular,Lipids,Fatty Acids,ACADL

    Molecular Weight

    47 kDa

    Gene ID

    33

    UniProt

    P28330

    Pathways

    Monocarboxylic Acid Catabolic Process
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