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ELISA analysis of ACACB protein using GTX89089 ACACB antibody, Internal. This antibody was used as a detecting antibody. Dilution : 1.5microg/ml
ELISA analysis of ACACB protein using GTX89089 ACACB antibody, Internal. This antibody was used as a detecting antibody. Dilution : 1.5microg/ml
ELISA analysis of ACACB protein using GTX89089 ACACB antibody, Internal. This antibody was used as a detecting antibody. Dilution : 1.5microg/ml

ACACB antibody, Internal

GTX89089
GeneTex
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetACACB
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Overview

  • Supplier
    GeneTex
  • Product Name
    ACACB antibody, Internal
  • Delivery Days Customer
    7
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID32
  • Target name
    ACACB
  • Target description
    acetyl-CoA carboxylase beta
  • Target synonyms
    ACC2; ACCB; ACC-beta; acetyl-CoA carboxylase 2; acetyl-Coenzyme A carboxylase beta; HACC275
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO00763
  • Protein Name
    Acetyl-CoA carboxylase 2
  • Scientific Description
    Acetyl-CoA carboxylase (ACC) is a complex multifunctional enzyme system. ACC is a biotin-containing enzyme which catalyzes the carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in fatty acid synthesis. ACC-beta is thought to control fatty acid oxidation by means of the ability of malonyl-CoA to inhibit carnitine-palmitoyl-CoA transferase I, the rate-limiting step in fatty acid uptake and oxidation by mitochondria. ACC-beta may be involved in the regulation of fatty acid oxidation, rather than fatty acid biosynthesis. There is evidence for the presence of two ACC-beta isoforms. [provided by RefSeq, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • DEHP deregulates adipokine levels and impairs fatty acid storage in human SGBS-adipocytes. Schaedlich K et al., 2018 Feb 22, Sci Rep
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