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Amphasys

Ampha X30

Short product description
Impedence flow cytometry of another dimension

Information

Impedance Flow Cytometry provides a straightforward and cost-efficient solution for single-cell analysis, eliminating the need for dyes, markers, and incubation. Cell viability, cell count, and cell metabolic status can be determined quickly and with minimal effort.  

  • Viability, counting, cell metabolic status, including apoptosis 
  • Real-time monitoring of cell cultures 
  • Label-free analysis of all cell types 
  • Works with turbid, opaque, and auto-fluorescent media 
  • Cost-efficient in investment, maintenance, and cost per sample 
  • Portable and desktop solutions 

 

Cell Analysis with Ampha X30

The novel Ampha X30 opens a new era of cell analysis: simultaneous measurement of cell count and cell viability, and in addition more information about the status of the cells, like metabolic activity. Results are available after minutes – including sample preparation! With one instrument and four different chip sizes of the microfluidic chip the whole range of cells can be measured: bacteria, human and animal cells, algae, yeast, and others like somatic cells in milk.

all cell types can be analyzed with one instrument, using chips with different channel diameters. The cells are not harmed by the measurement and due to the absence of dyes and markers, the cells can be recovered and reused, e.g., for sorting or tissue culture.

 

Efficient

For the sample preparation no markers or dyes are required which reduces the operational cost. In addition, no incubation time is needed which shortens the whole measurement to minutes – from sample preparation until the result.

 

Flexible

The instrument is highly flexible and can be used for online analysis via a bypass of the reaction solution. The sample can be pumped from the reactor directly through the microfluidic chip and back into the reactor. The sophisticated software thereby facilitates measurement and data analysis and integrated wizards promote a simple workflow.

 

Your Benefits:

  • No labeling, no staining, no incubation
  • No calibration
  • Short sample preparation, short measuring times, immediate results
  • Highly sophisticated software for operation and data analysis
  • Simultaneous analysis of cell viability, counting and other cell properties
  • Cell sizes between 1 µm and 50 µm
  • Low operational costs
  • Online measurements via bypass possible
  • Case study: Yield fermentation

    Monitoring cell health status is essential to avoid cell culture loss.

    An example performed in yeast culture shows the health status on different measurement days after starting the fermentation.

    Until the end of day 1 (red), the yeast culture moved from the lag to early exponential (log) phase. Significant cell proliferation occurs in the exponential growth phase which takes place between day 1 to day 2 (green). Due to the strong proliferation and a depletion of the nutrients, the viable population (blue) further shifts to lower phase angles until the end of day 3. This information shows the yeast cells health status and allows an early detection of fermentation issues and helps to troubleshoot the problems.

  • Case Study: Efficacy of Antibiotic Compounds

    Amphasys’ technology enables to determine the efficacy of antibiotic compounds on bacterial cultures quickly and easily. To carry out the measurement, neither markers nor staining dyes are needed, and an incubation overnight is not necessary neither.

    An unknown strain of E. coli was prepared in three samples and Ampicillin was added in 1.6 mg and 160 mg doses. Samples were measured 1 hour, 3 hours and 25 hours after the treatment.

    The figure shows the measured cell concentration of the bacteria. A timely monitoring of the efficacy of the applications allows to find the right treatment in an easy, very fast and accurate way.

  • Case Study: Apoptosis Monitoring

    The detection of apoptosis is a special case in cell analysis and requires so far dedicated equipment and longer assay times. In a study, the effect of Staurosporine on Burkitt lymphoma cells BL2 was investigated.

    The response of BL2 cells to Staurosporine treatment was realized in a time course experiment. In the figure, the control sample (black line) shows activity for more than 10 hours before decreasing in viability. The treatment of the cell line with Staurosporine shows a fast and significant reduction of viability shortly after one hour. Measurements of the cell samples with the Ampha X30 can be performed immediately after sample preparation – without any delay for induction or incubation.

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