Overview

Description

  • NatureSynthetic
  • Amino Acid Sequence
    • SpeciesHuman
    • SequenceTILTYPFKNLPT-C
    • Amino acids2 to 13

Associated products

Specifications

Our Abpromise guarantee covers the use of ab23180 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

  • Applications

    Blocking - Blocking peptide for Anti-HADHB antibody (ab10093)

  • FormLiquid
  • Concentration information loading...

Preparation and Storage

  • Stability and Storage

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

General Info

  • Alternative names
    • 2 enoyl Coenzyme A (CoA) hydratase beta subunit
    • 3 ketoacyl Coenzyme A (CoA) thiolase of mitochondrial trifunctional protein beta subunit
    • 3 ketoacyl Coenzyme A thiolase
    • 3 ketoacyl Coenzyme A thiolase of mitochondrial trifunctional protein beta subunit
    • 3-ketoacyl-CoA thiolase
    • Acetyl CoA acyltransferase
    • Acetyl-CoA acyltransferase
    • Beta ketothiolase
    • Beta-ketothiolase
    • ECHB
    • ECHB_HUMAN
    • HADH
    • Hadhb
    • Hydroxyacyl CoA dehydrogenase/3 ketoacyl CoA thiolase/enoyl CoA hydratase (trifunctional protein), beta subunit
    • Hydroxyacyl Coenzyme A (CoA) dehydrogenase beta subunit
    • Hydroxyacyl Coenzyme A dehydrogenase
    • Hydroxyacyl Coenzyme A dehydrogenase beta subunit
    • Hydroxyacyl Coenzyme A dehydrogenase/3 ketoacyl Coenzyme A thiolase/enoyl Coenzyme A hydratase (trifunctional protein) beta subunit
    • MGC87480
    • Mitochondrial trifunctional enzyme beta subunit
    • Mitochondrial trifunctional protein beta subunit
    • MSTP 029
    • MSTP029
    • MTPB
    • TP beta
    • TP-beta
    • TPbeta
    • Trifunctional enzyme subunit beta
    • Trifunctional enzyme subunit beta mitochondrial
    • Trifunctional protein
    see all
  • PathwayLipid metabolism; fatty acid beta-oxidation.
  • Involvement in diseaseDefects in HADHB are a cause of trifunctional protein deficiency (TFP deficiency) [MIM:609015]. The clinical manifestations are very variable and include hypoglycemia, cardiomyopathy and sudden death. Phenotypes with mainly hepatic and neuromyopathic involvement can also be distinguished. Biochemically, TFP deficiency is defined by the loss of all three enzyme activities of the TFP complex.
  • Sequence similaritiesBelongs to the thiolase family.
  • Cellular localizationMitochondrion.
  • Information by UniProt

References for Human HADHB peptide (ab23180)

ab23180 has not yet been referenced specifically in any publications.

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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"