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HADH antibody

This Rabbit Polyclonal antibody specifically detects HADH in WB, IHC, ELISA and IP. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN5702281

Quick Overview for HADH antibody (ABIN5702281)

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

  • 41
  • 14
  • 1
  • 1
Rabbit

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
  • 15
  • 14
  • 13
  • 13
  • 11
  • 9
  • 9
  • 8
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunoprecipitation (IP)
  • Immunogen

    hydroxyacyl-Coenzyme A dehydrogenase

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    HepG2 cells were subjected to SDS PAGE followed by western blot with FNab03747(HADH antibody) at dilution of 1:500

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide and 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Expiry Date

    12 months
  • Target

    HADH (Hydroxyacyl-CoA Dehydrogenase (HADH))

    Alternative Name

    HADH

    Background

    Synonyms:HAD, HADHSC, SCHAD Background:This gene is a member of the 3-hydroxyacyl-CoA dehydrogenase gene family. The encoded protein functions in the mitochondrial matrix to catalyze the oxidation of straight-chain 3-hydroxyacyl-CoAs as part of the beta-oxidation pathway. Its enzymatic activity is highest with medium-chain-length fatty acids. Mutations in this gene cause one form of familial hyperinsulinemic hypoglycemia. The human genome contains a related pseudogene of this gene on chromosome 15.

    Molecular Weight

    34 kDa

    Gene ID

    3033

    UniProt

    Q16836

    Pathways

    Negative Regulation of Hormone Secretion, Monocarboxylic Acid Catabolic Process
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