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Phospholipase D Assay Kit

AcA
Produktnummer ABIN1000328

Kurzübersicht für Phospholipase D Assay Kit (ABIN1000328)

Target

Alle Phospholipase D (PLD) Kits anzeigen
Phospholipase D (PLD)

Applikation

Activity Assay (AcA)
  • Spezifität

    0.04 U/L

    Produktmerkmale

    Sensitive. Use 10 µL samples. Detection range: colorimetric assay 0.06 - 10 U/L, fluorimetric assay 0.04 - 1 U/L.
    Simple and High-throughput: the assay involves addition of a single working reagent and can be readily adapted to high-throughput assays for drug screening.

    Bestandteile

    Assay Buffer: 10 mL. Dye Reagent: 120 µL. Enzyme Mix: 120 µL. Substrate: 1.5 mL. Calibrator: 400 µL.

    Benötigtes Material

    Pipetting devices, centrifuge tubes, clear flat-bottom uncoated 96-well plates, optical density plate reader, black flat-bottom uncoated 96-well plates, fluorescence plate reader.
  • Applikationshinweise

    Direct Assays: phospholipase D in biological samples.
    Drug Discovery/Pharmacology: effects of drugs on phospholipase D metabolism.

    Ergebnisberechnung

    Subtract blank value (#4) from the standard values and plot the OD or F against standard concentrations.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Lagerung

    -20 °C
  • Target

    Phospholipase D (PLD)

    Andere Bezeichnung

    Phospholipase D

    Hintergrund

    Quantitative determination of phospholipase D activity by colorimetric (570nm) or fluorimetric (530/590nm) method.
    Procedure: 30 min.

    Phospholipase D (PLD) catalyses the hydrolysis of the phosphodiester bond of glycerophospholipids to generate phosphatidic acid and a free headgroup. Abnormalities in PLD expression have been associated with human cancers. This method provides a simple and high-throughput assay for measuring PLD activity. In this assay, PLD hydrolyzes phosphatidylcholine to choline which is determined using choline oxidase and a H2O2 specific dye. The optical density of the pink colored product at 570nm or fluorescence intensity (530/585 nm) is directly proportional to the PLD activity in the sample.
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