Cell Count Normalization Kit

∼ Features ∼

  • Enhance reliability of data on plate assay
  • No need for lysis procedure
  • Easily determine cell number just by adding the reagent

For information about measuring cell senescence via plate reader, Click Here for the product page.

For information about measuring glucose levels, Click Here for the product page.


Product Description

Cell Count Normalization Kit employs a nucleic acid staining dye, Hoechst 33342 which binds to nuclear DNA to emit blue fluorescence. By measuring this blue fluorescence, correction of the measured value can easily be carried out in simple steps whereas the visual cell counting method requires cumbersome procedure. Moreover, unlike the correction by protein or ATP amount, the kit requires no lysis procedure. In addition, Quenching Buffer included in the kit enables a direct measuring of fluorescence signal without any background.

Necessity of normalization

When cells are analyzed in a microplate, the results obtained may sometimes differ depending on the number of cells per well. In such cases, normalization of the measured values will be necessary.

Comparison with conventional method

Normalization of the measured values at the time of plate assay is done by using the cell number or nucleus/protein level as an indicator. Among these detection techniques, our nuclear staining kit is easy-to-use and capable of analyzing multiple specimens.

*1 In experiment the number of nuclei varies, it may differ from the actual cell number.

*2 In experiment protein level fluctuates, it may be different from the actual cell number.

High correlation with cell number

When you are performing a plate assay the data needs to be normalized. In order to normalize the data, an assessment method equivalent (i.e. cell counting) is essential. In the experiments below, changes in fluorescence intensity were confirmed by cell number-dependents. Data at the time of plate assay were normalized by using this kit and the cell counting method. A comparison was then made between the two methods.

Cell number-dependent changes in fluorescence intensity

Cell number-dependent changes in fluorescence intensity were observed, and the results were highly linear.

HeLa cells were serially diluted and seeded in a 96-well microplate. After incubation overnight, fluorescence intensity was measured using this kit.

Comparison with cell counting method

When normalization occurred at the time of the plate assay (lactate measurement), this kit showed equivalent results to cell counting.

2-Deoxy-D-glucose was added to HeLa cells. Lactate levels in the supernatant were quantified using the Lactate Assay Kit-WST (Item#: L256)

Storage Condition: Store at 0-5 oC and protect from light.

Kit Contents:

Item # Description/Size Availability Qty Break Price Quantity
1,000 tests
1-2 business days 1 $200.00
200 tests
1-2 business days 1 $80.00

*Your estimated shipping date is calculated based on production, payment method, destination, and your shipping option.
For Research Use Only Products