MilliporeSigma
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11644793001

Roche

Cytotoxicity Detection Kit (LDH)

suitable for protein quantification, suitable for cell analysis, detection, sufficient for ≤2,000 tests

Synonym(s):
LDH

usage

sufficient for ≤2,000 tests

Quality Level

packaging

pkg of 1 kit

manufacturer/tradename

Roche

technique(s)

protein quantification: suitable

λmax

490 nm

application(s)

cell analysis
detection

detection method

colorimetric

storage temp.

−20°C

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This Item
TOX8CYTODET-ROSCR150
usage

sufficient for ≤2,000 tests

usage

 kit sufficient for 2,000 tests

usage

sufficient for 2,000 multiwell tests (04744934001), sufficient for 400 multiwell tests (04744926001)

usage

-

packaging

pkg of 1 kit

packaging

pkg of 1 kit

packaging

kit of 1 (4 components)

packaging

-

manufacturer/tradename

Roche

manufacturer/tradename

-

manufacturer/tradename

Roche

manufacturer/tradename

-

λmax

490 nm

λmax

-

λmax

490-492 nm

λmax

-

application(s)

cell analysis
detection

application(s)

cell analysis
detection

application(s)

cell analysis
detection

application(s)

-

General description

A nonradioactive alternative to the [51Cr] and [3H]-thymidine release assay.
Colorimetric assay for the quantification of cell death and cell lysis, based on the measurement of lactate dehydrogenase (LDH) activity released from the cytosol of damaged cells into the supernatant.

Application

The Cytotoxicity Detection Kit (LDH) is a fast and simple method to quantify cytotoxicity/cytolysis based on the measurement of LDH activity released from damaged cells using the 96-well plate format. Thus, the kit can be used in many different in vitro cell systems when damage to the plasma membrane occurs. For example:
  • Detection and quantification of cell-mediated cytotoxicity
  • Determination of mediator-induced cytolysis
  • Determination of the cytotoxic potential of compounds in environmental and medical research, and in the food, cosmetic, and pharmaceutical industries
  • Determination of cell death in bioreactors
  • Testing of biocompatibility of various scaffolds, employed in bone tissue engineering, for bone cell growth

Packaging

1 kit containing 2 components.

Preparation Note

Working solution: Vial 1 Catalyst:
Reconstitute the lyophilisate in 1 ml double dist. water for 10 minutes and mix thoroughly.

Vial 2 Dye solution:
Ready-to-use solution.

Reaction mixture
For 100 tests: Shortly before use, mix 250 μl of vial 1 with 11.25 ml of vial 2.
For 400 tests: Shortly before use, add the total volume of catalyst (1 ml) to the total volume
of dye solution (45 ml) and mix well.

Note: The Reaction mixture should not be stored; prepare immediately before use.
Storage conditions (working solution): 2 to 8 °C
The lyophilizate is stable at 2 to 8 °C.
The reconstituted catalyst solution is stable for four weeks when stored at 2 to 8 °C.
Once thawed, the dye solution is stable for several weeks when stored at 2 to 8 °C.

Other Notes

For life science research only. Not for use in diagnostic procedures.

Kit Components Only

Product No.
Description

  • Catalyst (Diaphorase/NAD+ mixture)

  • Dye Solution (INT and sodium lactate)

related product

Product No.
Description
Pricing

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


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Sabine Sewing et al.
PloS one, 11(7), e0159431-e0159431 (2016-07-22)
Single stranded oligonucleotides (SSO) represent a novel therapeutic modality that opens new space to address previously undruggable targets. In spite of their proven efficacy, the development of promising SSO drug candidates has been limited by reported cases of SSO-associated hepatotoxicity.
Guo-qian He et al.
Molecular brain, 8, 88-88 (2015-12-25)
Growth arrest and DNA-damage inducible protein 45 beta (Gadd45b) is serving as a neuronal activity sensor. Brain ischemia induces the expression of Gadd45b, which stimulates recovery after stroke and may play a protective role in cerebral ischemia. However, little is
Volker Gassling et al.
Clinical oral implants research, 24(3), 320-328 (2011-11-19)
The loss of jaw bone caused by different kinds of pathologies leads to dysfunction and reduced quality of life in affected patients. Thus, the pivotal goal in bone tissue engineering is to reconstruct these defects. The essential precondition for new
Mélanie Morin-Brureau et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 31(29), 10677-10688 (2011-07-22)
Recent studies suggest that blood-brain barrier (BBB) permeability contributes to epileptogenesis in symptomatic epilepsies. We have previously described angiogenesis, aberrant vascularization, and BBB alteration in drug-refractory temporal lobe epilepsy. Here, we investigated the role of vascular endothelial growth factor (VEGF)
Patrick H Warnke et al.
Tissue engineering. Part C, Methods, 15(2), 115-124 (2008-12-17)
Selective laser melting (SLM), a method used in the nuclear, space, and racing industries, allows the creation of customized titanium alloy scaffolds with highly defined external shape and internal structure using rapid prototyping as supporting external structures within which bone

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Cytotoxicity Detection Kit (LDH) Protocol & Troubleshooting

Cytotoxicity Detection Kit (LDH) Protocol & Troubleshooting

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