Cytotoxicity Detection Kit (LDH)

Description

• 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 cytotoxicityDetermination of mediator-induced cytolysisDetermination of the cytotoxic potential of compounds in environmental and medical research, and in the food, cosmetic, and pharmaceutical industries[1][2][3]Determination of cell death in bioreactorsTesting of biocompatibility of various scaffolds, employed in bone tissue engineering, for bone cell growth[4][5]
• 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 mixtureFor 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 volumeof 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 °CThe 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: 2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research