An In Vitro Fluorescence Assay for Renal Cel Viability and Function




The Easy and Rapid In Vitro Research Fluorescence Assay for Kidney Cells

Cell Population Species Medium Formulation Catalog Number Quantity
Renal cells (adherent) Any User defined KRF-A-1 1 Kit
Renal cells (non-adherent) Any User defined KRF-NA-1 1 Kit

Renal Fluor™: An In Vitro Fluorescence Assay for Renal Cell Viability and Function


  • Determine the metabolic viability of different kidney cell types.
  • Study factors produced by different kidney cells types in culture, e.g. erythropoietin.
  • Determine metabolic/mitochondrial dysfunction in kidney cells.
  • Study the effect of agents on kidney function in different renal cell types.
  • Study mechanisms of renal injury.
  • Study renal disorders at the cellular and genetic levels.
  • Incorporates a non-destructive, highly accurate alamarBlue™ fluorescence reagent.
  • Uses a fluorescence plate reader or multimode plate reader with an excitation filter at 560nm and an emission filter at 590nm.
  • Non-subjective, instrument-based and quantitative readout procedure.
  • Easily multiplexes with other fluorescent labels/markers.
  • Combine with gene expression assays etc or other endpoints for more information from a single sample.
  • Flexibility to use the investigators own growth medium and protocols.
  • High throughput capability.
  • Results in 1-3 hours after adding reagent.
  • Simple, time efficient and cost effective.

Principle of Using STEMFluor to Measure Cell Proliferation using a Fluorescence Resazurin Readout

RenalGlo™ can be used for multiple species. Primary kidney cells as well as kidney cell lines, such as HepG2. Many kidney cell types have a high level of metabolic activity that can be used to determine changes in metabolic viability and other functions.

  • Incorporates the measurement of non-fluorescent Resazurin (alamarBlue™) to fluorescent Resorufin in an oxidation/reduction reaction that occurs only in live cells. The amount of fluorescence (relative fluorescence units, RFU) is dependent on the metabolic status of the cells and therefore is not only a measure of metabolic viability, but cell proliferation or inhibition.
  • After culture, add 10μL of reagent, mix and measure signal between 30 minutes and 4 hours in a fluorescence plate reader.
  • Uses a plate fluorometer or multi mode plate reader to measure fluorescence with an excitation filter 560nm and an emission filter of 590nm.

For Research Use Only. Not for clinical diagnostic use.
Fluorescence or multimode plate reader with a 560nm excitation and 590nm emission filter.

  • AlamarBlue™/Resazurin Reagent.
  • 3% SDS solution to stop the reaction.
  • Resorufin to standardize the assay.
  • Non-sterile, black, 96-well plates for assay standardization.
  • Sterile, black, 96-well plates, for neural cell culture. Choice of adherent or non-adherent plates.
  • Sterile, adhesive foil covers to maintain sterility of unused wells.
PLEASE NOTE. The investigator has the flexibility to culture renal cells using their own growth medium. RenalGro™ Growth Medium is available separately from Preferred Cell Systems™.