Exicycler™ 384 Real-Time Quantitative Thermal Block utilizes 384-wll plate which uniformly detects excited light, excitation light blocking technology and a 2D sensor. Those allow minimized optical sensitivity and deviation between wells during the real-time gene amplification. Furthermore, 384 samples can be tested even with a miniscule volume of 5 μl, making it an excellent competitive instrument for analyzing many samples.
Optical Patent Technology
Bioneer patented fluorescence detection method (Korean Patent No. 10-1089045, US Patent No. US 8427643) was applied to minimize noise caused by reflected light, thus improving sensitivity and accuracy.
Figure. Separation of a reflection light from fluorescence
* Noise caused by reflected light: The fluorescent materials used in qPCR create emission when the absorbed excitation energy excites them then falls to the ground state. In conventional qPCR instruments, part of excited light irradiated from the sample is reflected from the surface of the plate and the instrument, which may enter the detector to be also mistakenly read as part of the light from the sample. As the excited light has much more luminance than the fluorescent light, reflected light also contain high luminance, making it unable to be completely removed by the fluorescent light and creating noise in the process, deteriorating sensitivity and accuracy. However, by using our patented technology, excitation and fluorescence have different polarity, allowing the reflect light unable to be blocked by fluorescent filter to be filtered once again through polarizing filter. This allows drastic reduction of noise caused by reflected light compared with other qPCR instruments.
Enables large-scale analysis at minimum cost and time with accurate results from 5 μl of reaction solution
Highly reproducible and accurate results by light tunnel (LT) technology (Korean Patent No. KR 0794703, US Patent No. 8139210, Japanese Patent JP 4751821, China Patent No. CN 1798969) irradiating uniform excitation light, excitation light interception method (Korean Patent No. 10-1089045 and US Pat. No. 8427643) using polarization, and a 96-well simultaneous detection technique using a 2-D sensor minimizing optical sensitivity and deviation between well
Maximum ramping rate of 4.5 ℃/sec (Exicycler ™ 96 Fast: max 5.0 ℃/sec) decreases reaction time by using a unique thermal block and temperature control technology
Simultaneous detection of five targets capable of being used in multiplex PCR without the need of reference dyes, used for the compensation of light quantity deviation, through the uniform optical system patent technology (Korean Patent KR 0794703, US Patent US 8139210, Japanese Patent JP 4751821, China Patent CN 1798969)
Diverse choice of fluorescent dyes including the universal ones with wide excitation/emission wavelength detection range being 475 to 690nm, unlike other traditional instruments designed for specific dyes
Large detection range being more than 9 log allowing DNA detection and qualitative analysis even at low and high concentration samples using a short Arc lamp, a powerful excitation light source
Simplified search of optimal PCR annealing temperature with temperature gradients from 1~20°C available in the range of 20~95°C
Wide applications such as touch down PCR through time increment and temperature increment adjustment functions
Accessible User-centric GUI for easy operation and manipulation for designing experiments and analyzing results
• Gene expression analysis
• MicroRNA expression analysis
• Gene copy number analysis
• Pathogen detection
• Genetic mutation test
• GMO quantitative and qualitative test
