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HADH antibody (AA 57-314)

This anti-HADH antibody is a Chicken Polyclonal antibody detecting HADH in WB. Suitable for Human, Mouse and Rat.
Catalog No. ABIN2468091

Quick Overview for HADH antibody (AA 57-314) (ABIN2468091)

Target

See all HADH Antibodies
HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

Reactivity

  • 40
  • 37
  • 22
  • 8
  • 5
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Human, Mouse, Rat

Host

  • 42
  • 14
  • 1
Chicken

Clonality

  • 44
  • 13
Polyclonal

Conjugate

  • 28
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HADH antibody is un-conjugated

Application

  • 42
  • 16
  • 15
  • 13
  • 13
  • 12
  • 9
  • 9
  • 8
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 57-314

    Purification

    Immunoaffinity Purified
  • Application Notes

    Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial antibody can be used for the detection of Short chain 3-hydroxyacyl-CoA dehydrogenase, mitochondrial by Western Blot.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline. No preservatives added.

    Preservative

    Without preservative

    Handling Advice

    As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

    Storage

    4 °C/-20 °C

    Storage Comment

    HADHSC antibody can be stored at 4 °C for short term (weeks). Long term storage should be at -20 °C.
  • Target

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    Alternative Name

    HADHSC

    Background

    FUNCTION: Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts it highest activity toward 3-hydroxybutyryl-CoA.

    DISEASE: Defects in HADHSC are the cause of 3-alpha-hydroxyacyl-CoA dehydrogenase deficiency (HAD deficiency) [MIM:609609]. HAD deficiency is a metabolic disorder with various clinical presentations including hypoglycemia, hepatoencephalopathy, myopathy or cardiomyopathy, and in some cases sudden death.

    Molecular Weight

    34.3 kDa (calculated)

    Gene ID

    3033

    NCBI Accession

    NP_005318

    UniProt

    Q16836

    Pathways

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
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