Name: CytoCHECK SPAchip® pH red single detection kit - CytoCHECK SPAchip® pH red single detection kit
SKU: A4C-S-001-PHR
Price: 488.72 GBP
Availability: InStock

CytoCHECK SPAchip® pH red single detection kit

SKU: A4C-S-001-PHR UNSPSC: 41105332 Manufacturer Part No: S-001-PHR Pack Size: 1

Measures intracellular pH levels by changes in fluorescence intensity.
Composed of fluorescently labeled silicon microparticles that can be internalized in the cytosol of cultured cells.
Provides a more comprehensive study of single-cell physiology and metabolism.
Maximizes the performance of most imaging analyzers.
Non-invasive and allows long-term monitoring of intracellular pH changes.

CytoCHEK SPAchip® assay kits are novel fluorescence cell- based assays developed by A4cell that brings together the fields of nanotechnology and cell biology. SPAchips are composed of fluorescently labeled silicon microparticles which can be internalized in the cytosol of cultured cells to monitor intracellular parameters for extended periods of time..

CytoCHECK SPAchip® pH RED Single-Detection Kit allows measurement of intracellular pH levels by changes in fluorescence intensity, which allows a more comprehensive study of the living single-cell physiology and maximizes the performance of most of imaging analyzers. Its signal in red makes it feasible for applications with high green autofluorescence such as organoids cultures. Moreover, due to its ratiometric behaviour signal to noise ratio is increased leading to cleaner curves.

Imaging and fluorescence signal analysis

SPAchip® kits are designed to dynamically shift fluorescence intensity values in response to intracellular changes in analyte concentration. Fluorescence intensity is measured by exciting the live cell sample at 546 nm and detecting fluorescence emission at 610 and 707 nm. Normalization of fluorescence intensity values collected at both emission wavelengths provide a ratiometric behavior that allows a more precise quantification of intracellular pH. Relative intensity units depend on the instrumental setup (excitation power, detector efficiency, etc). To obtain quantitative data, a calibration curve needs to be analyzed in the same run. Data acquisition can be adapted to fluorescence microscopy and flow cytometry. Additional detection channels, such as brightfield, phase contrast, FSC or SSC, are suggested to better identify individual SPAchips.