The Cellometer™ K2 fluorescent cell counter is an advanced, dual-fluorescence cell counter with built-in assays and cell types for the analysis of hepatocytes, stem cells, splenocytes, tumor suspension, and other complex primary cells. A 21 CFR Part 11 module is available.
For research use only. Not for use in diagnostic procedures.
The Cellometer K2 fluorescent cell counter, powered by Matrix software, utilizes brightfield imaging and dual-fluorescence imaging to quickly and accurately identify and count individual cells. Cell count, concentration, diameter, and % viability are automatically calculated and reported.
The Cellometer K2 cell counter provides:
The Cellometer K2 can be configured to handle a variety of cell types, including primary cells, tumor digest, insect cells, cell lines, fragile cells, and more at low or high concentrations.
Take the guesswork out of setting up your cell quantification experiments. The Cellometer K2 includes a library of commonly-used assays and cell types with predefined settings to help improve consistency of results. Conveniently build and modify assays and cell types to help match your specific experimental requirements.
Capture one, four, or eight images per sample. The instrument default is set to four images, which is the equivalent of six quadrants on a hemocytometer. Eight images are equivalent to twelve quadrants on a hemocytometer. The ability to capture multiple images improves the cell counting dynamic range and reliability of results.
The fluorescent image shows bright green AO-positive hepatocytes declustered by the Cellometer K2 algorithm. Red circled hepatocytes are PI-positive (dead) while free nuclei are not counted.
Use default or customized reports based on the data and images you want to be included for your specific experimental needs. Automatically export images and data reports including CSV, Excel, Word, or PDF files. Perform statistical analysis for a wide range of parameters such as average, variance, min/max, and standard deviation of cell size.
An optional module can be purchased to facilitate 21 CFR Part 11 compliance. The additional module comes with the following features:
Why dual-fluorescence?
Because brightfield cell counting does not differentiate nucleated from non-nucleated cells and Trypan blue staining is not as easy to detect as fluorescent staining, dual-color fluorescence is strongly recommended for reliable viability analysis for primary cells. The K2 is equipped with standard assays for dual-fluorescence analysis of a variety of cells stained with Acridine Orange and Propidium Iodide (AO/PI).
The AO/PI method
Acridine Orange (AO) is a nuclear staining (nucleic acid binding) dye permeable to both live and dead cells. It stains all nucleated cells to generate green fluorescence. Propidium Iodide (PI) can only enter dead cells with compromised membranes. It stains all dead nucleated cells to generate red fluorescence. Cells stained with both AO and PI fluoresce red due to quenching, so all live nucleated cells fluoresce green and all dead nucleated cells fluoresce red.
No interference from red blood cells, platelets, or debris
The dual-fluorescence AO/PI method utilizes nuclear staining dyes that bind to nucleic acids in the cell nucleus. Because most mature mammalian red blood cells do not contain nuclei, only live and dead mononuclear cells produce a fluorescent signal. There is no need to lyse red blood cells, saving time and eliminating an extra sample preparation step. Red blood cells, platelets, and debris are not counted in the fluorescent channels.
NCI-60 and clumpy MCF-7 cells
NCI-60 is a group of 59 human cancer cell lines (originally 60) developed by the National Cancer Institute (USA) for screening purposes.
Clumpy cells
Irregular-shaped cells
Counting 1 x 106 cells takes approximately 5 minutes with a manual hemacytometer. Counting live and dead cells sometimes takes twice as long. The Cellometer K2 cell counter calculates cell count and concentration for live and dead cells and % viability in just 60 seconds.
Improve data reliability and consistency:
We offer two different disposable counting slides, one with protective coverings on both sides and a ready-to-use option packed in microscope slide boxes. Disposable slides offer the advantages of time-saving, since no washing is required, reduced risk of contamination and reduced biohazard risk to users.
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Imaging performance |
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PC / Laptop Minimum Requirements: (If purchasing Cellometer without PC laptop) |
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Available fluorescence optics modules |
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Cellometer
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Unit Size |
1 Each
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Cell counting plays a crucial role in the development and manufacturing of cell and gene therapies as well as regenerative...
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