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Signal Transduction Metabolism Energy Metabolism

Phosphoenolpyruvate Carboxylase Assay Kit (Colorimetric) (ab239720)

Phosphoenolpyruvate Carboxylase Assay Kit (Colorimetric) (ab239720)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Detection method: Colorimetric
  • Platform: Microplate reader
  • Sample type: Adherent cells, Suspension cells

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Overview

  • Product name

    Phosphoenolpyruvate Carboxylase Assay Kit (Colorimetric)
  • Detection method

    Colorimetric
  • Sample type

    Adherent cells, Suspension cells
  • Product overview

    Phosphoenolpyruvate carboxylase (PPC) is an enzyme found in plants and some types of bacteria that catalyzes the formation of oxaloacetate from phosphoenolpyruvate (PEP) by fixing one carbon in the forms of either carbon dioxide or bicarbonate. PPC participates in carbon fixation in C4 photosynthesis and Crassulacean acid metabolism (CAM) in plants and acts as an anaplerotic enzyme, which replenishes TCA cycle intermediates, in bacteria and C3 plants. The participation of PPC in the carbon fixation cycle of C4 plants enable them to survive in high sunlight but dry environments.


    Phosphoenolpyruvate Carboxylase Assay Kit (Colorimetric) (ab239720) provides a quick and easy method for the measurement of PPC activity in various samples. In this assay, PPC is coupled with a set of enzymes that convert PEP and carbonate into a series of intermediates and hydrogen peroxide, which in turn, reacts with a probe and converter generating a colorimetric signal (OD 570 nm). The generated absorbance signal is directly proportional to the amount of active PPC present in the samples. This kit provides a simple, fast and high throughput adaptable assay to measure the activities of PPC as low as 0.2 Mu.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at -20°C. Please refer to protocols.
  • Components 100 tests
    PPC Assay Buffer 1 x 25ml
    PPC Enzyme Mix 1 vial
    PPC Positive Control 1 vial
    PPC Probe (in DMSO) 1 x 220µl
    PPC Standard (100 mM) 1 x 100µl
    PPC Substrate A 1 vial
    PPC Substrate B 1 x 220µl
  • Research areas

    • Signal Transduction
    • Metabolism
    • Energy Metabolism
    • Metabolism
    • Pathways and Processes
    • Metabolic signaling pathways
    • Energy transfer pathways
    • Energy Metabolism
  • Relevance

    Major sites of expression of PEP Carboxylase are liver, kidney and adipocytes. PEP carboxylase, along with GTP, catalyzes the formation of phosphoenolpyruvate from oxaloacetate, with the release of carbon dioxide and GDP. The expression of this gene can be regulated by insulin, glucocorticoids, glucagon, cAMP, and diet. A mitochondrial isozyme of the encoded protein has also been characterized.
  • Cellular localization

    Cytoplasmic
  • Alternative names

    • PEPC 1
    • PEPCase 1
    • Phosphoenolpyruvate carboxylase 1

Images

  • PPC Assay Standard curve
    PPC Assay Standard curve
  • Phosphoenolpyruvate Carboxylase activities in Spinach leaf extract (8 µg protein), E. coli lysate (11 µg protein) & PPC positive control.
    Phosphoenolpyruvate Carboxylase activities in Spinach leaf extract (8 µg protein), E. coli lysate (11 µg protein) & PPC positive control.
  • Specific PPC activities in Spinach leaves and E. coli cell lysate.
    Specific PPC activities in Spinach leaves and E. coli cell lysate.

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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