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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.

2310.00 SEK - 6340.00 SEK

Specifications

Cell Permeability Cell-impermeant
Color Red
Description CyQUANT™ LDH Cytotoxicity Assay, fluorescence
Detection Method Fluorescence
For Use With (Application) LDH Cytotoxicity Assay
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Product Code Brand Quantity Price Quantity & Availability  
16815171
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Invitrogen™
C20302
200 Assays
2310.00 SEK
1 set
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16616523
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Invitrogen™
C20303
1000 Assays
6340.00 SEK
Each
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Description

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.

Specifications

Specifications

Cell-impermeant
CyQUANT™ LDH Cytotoxicity Assay, fluorescence
LDH Cytotoxicity Assay
LDH Cytotoxicity Assay
560 nm
CyQUANT™
Red
Fluorescence
Microplate Reader
590 nm
96-well plate
Dry Ice
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For Research Use Only. Not for use in diagnostic procedures.