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Citrate synthase antibody [GT1761]

GTX628143
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetCS
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Overview

  • Supplier
    GeneTex
  • Product Name
    Citrate synthase antibody [GT1761]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    GT1761
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID1431
  • Target name
    CS
  • Target description
    citrate synthase
  • Target synonyms
    citrate (Si)-synthase; citrate synthase, mitochondrial
  • Host
    Mouse
  • Isotype
    IgG2a
  • Protein IDO75390
  • Protein Name
    Citrate synthase, mitochondrial
  • Scientific Description
    The protein encoded by this gene is a Krebs tricarboxylic acid cycle enzyme that catalyzes the synthesis of citrate from oxaloacetate and acetyl coenzyme A. The enzyme is found in nearly all cells capable of oxidative metablism. This protein is nuclear encoded and transported into the mitochondrial matrix, where the mature form is found. [provided by RefSeq]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Peroxisomal L-bifunctional protein (EHHADH) deficiency causes male-specific kidney hypertrophy and proximal tubular injury in mice. Ranea-Robles P et al., 2021 Sep, Kidney360
    Read more
  • Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis. Ranea-Robles P et al., 2021 Jul, Cell Mol Life Sci
    Read more
  • Structure-function analyses of the G729R 2-oxoadipate dehydrogenase genetic variant associated with a disorder of l-lysine metabolism. Zhang X et al., 2020 Jun 5, J Biol Chem
    Read more
  • DHTKD1 and OGDH display substrate overlap in cultured cells and form a hybrid 2-oxo acid dehydrogenase complex in vivo. Leandro J et al., 2020 May 8, Hum Mol Genet
    Read more
  • New evidence of exercise training benefits in myostatin-deficient mice: Effect on lipidomic abnormalities. Baati N et al., 2019 Aug 13, Biochem Biophys Res Commun
    Read more

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