7180980

Invitrogen™ CyQUANT™ LDH Cytotoxicity Assay, fluorescence

The CyQUANT LDH Cytotoxicity Assay, fluorescence, is a fluorescent assay that provides a simple and reliable method for determining cellular cytotoxicity.

Manufacturer: Fischer Scientific

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Cell Permeability

Cell-impermeant

Description

CyQUANT™ LDH Cytotoxicity Assay, fluorescence

For Use With (Application)

LDH Cytotoxicity Assay

Product Type

LDH Cytotoxicity Assay

Excitation Wavelength Range

560 nm

Product Line

CyQUANT™

Color

Red

Detection Method

Fluorescence

For Use With (Equipment)

Microplate Reader

Emission

590 nm

Format

96-well plate

Shipping Condition

Dry Ice

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Description

  • Lactate dehydrogenase (LDH) is a cytosolic enzyme present in many different cell types that is released into the cell culture medium upon damage to the plasma membrane
  • The CyQUANT LDH Cytotoxicity Assay, fluorescence, provides the reagents to accurately and quantitatively measure this extracellular LDH
  • The CyQUANT LDH Cytotoxicity Assay, fluorescence, features include: • Convenient —add-mix-read assay protocol for adherent and suspension cells, including 3D cell models • Accurate —provides a quantitative measurement of LDH release • Flexible —ideal for high-throughput screening, monitor cytotoxicity from the same sample over time • Robust —formulation with highly purified resazurin results in a large assay dynamic range LDH is a cytosolic enzyme present in many different cell types and is a well-established and reliable indicator of cellular toxicity
  • Damage of the plasma membrane results in a release of LDH into the surrounding cell culture medium
  • This extracellular LDH can be quantified by a coupled enzymatic reaction in which LDH catalyzes the conversion of lactate to pyruvate via NAD+ reduction to NADH
  • Diaphorase then uses NADH to reduce resazurin to resorufin that can be detected using an excitation of 560 nm and emission of 590 nm
  • The level of resorufin formation is directly proportional to the amount of LDH released into the medium
  • As a consequence of the synthesis and manufacturing processes, all resazurin-based reagents contain a detectable amount of resorufin contamination
  • The amount of contamination can vary greatly between sources of the material and manufacturing conditions, contributing to differences in detectable background fluorescence
  • More importantly, the contaminating resorufin reduces the signal to background ratio and dynamic range of the assay
  • An innovative process was developed that removes the contaminating resorufin, resulting in the highly pure resazurin used in the CyQUANT™ LDH Cytotoxicity Assay, fluorescence
  • The CyQUANT LDH Cytotoxicity Assay, fluorescence, provides the reagents needed for the simple, reliable fluorescence-based quantification of cellular cytotoxicity
  • The kit can be used with different cell types, including 3D cell models, to measure cytotoxicity mediated by chemical compounds as well as cell-mediated cytotoxicity
  • Since LDH in the medium is the indicator of cellular cytotoxicity, the assay can be used to monitor cytotoxicity from the same sample over time
  • To perform the assay, an aliquot of the cell culture medium is transferred to a new plate and the reaction mixture is added
  • After a 10-minute incubation, the reaction is stopped by adding Stop Solution and fluorescence is measured using a microplate reader.

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