Tm value uniformity (A) and Cq value uniformity (B).

Twenty four replicate reactions amplifying Lambda DNA (0.5 ng/20 μL) with Thermo Scientific DyNAmo Color Flash SYBR Green Master Mix were used to demonstrate the temperature and Cq uniformity across the 24-well plate. Tm values (A) or Cq values (B) were subtracted from the average value of 24 replicates and plotted by well position.
Block and heatsink

The patent pending block and heatsink design enable fast and uniform temperature control for the entire plate area.
Triplicate multiplexed reactions

Triplicate multiplexed reactions amplifying Staphylococcus sp., Streptococcus agalactiae, Streptococcus uberis DNA (100,000 to 100 copies/20 μL) and internal control (100,000 copies of Lambda DNA/20 μL) using Thermo Scientific DyNAmo Flash Probe qPCR Master Mix. Amplification and standard curves shown for each channel.
Schematic view of PikoReal's optical system and light paths.

The channel selection of the optical system is built on a motorized linear shuttle that moves to five channel positions. Each of the positions contains separate LED light sources, reflector, excitation filter, dichroic mirror and emission filter.
Schematic view of PikoReal's optical system and light paths.

Allelic discrimination

Triplicate reactions amplifying human gDNA (1 ng/20 μL) using ABI TaqMan SNP Genotyping Assay for rs1061666 (Assay ID: C_1420362_10, Gene name: Hypothetical LOC339290) and Thermo Scientific DyNAmo SNP Genotyping Master Mix. The results are shown both on RFU-RFU scatter plot and on plate grid. DyNAmo SNP Genotyping Master Mix shows the three distinct genotypes, X, XY and Y.
Dynamic range

Triplicate reactions amplifying ALDOA from human HeLa cDNA (35 ng to 0.35 pg of total RNA equivalents/20 μL) using Thermo Scientific Solaris qPCR Gene Expression Assay and Master Mix. Amplification and standard curves shown for six 10-fold dilutions of template.
Temperature and Melting Curve Uniformity

Replicate reactions (24) amplifying Lambda DNA (0.5 ng/20 μL) using Thermo Scientific DyNAmo Color Flash SYBR Green Master Mix. The graph shows the melting curve and its first negative derivate.
Relative quantification

Triplicate reactions amplifying PPIH from HeLa cDNA (5 ng of total RNA equivalents/20 μL) using Thermo Scientific Solaris qPCR Gene Expression Assay and Solaris qPCR Master Mix. HeLa cells were transfected with Thermo Scientific Dharmacon ON-TARGETplus siRNA reagents targeting PPIH or Non-Targeting Control (siNTC).
Virtual Pipetting Tool

All experiment data is shown conveniently on a single page. User modifications to analysis parameters can be seen in real time.
Convenience in use

All experiment data is shown conveniently on a single page. User modifications to analysis parameters can be seen in real time.
Significant savings in energy and plastics consumption

A) Total estimated annual energy consumption of 96-well PikoReal vs. a conventional qPCR instrument. B) Estimated annual plastics consumption using 96-well Piko PCR plates vs, conventional 96-well microplates. The calculations are based on three qPCR runs per day and 1200 qPCR runs per year.
Annual running costs (% of competitor A)

Annual running costs of the Piko Real System are up to 80% lower than with competitor A Real-Time PCR instrument. Calculations based on combined running costs of instrument (including SYBR Green reagent, plastic consumables and energy consumption) based on manufacturers recommended reagent volume.
PikoReal 24-well and 96-well block formats

PikoReal is available in 24-well and 96-well block formats.
Piko format – full compatibility

Piko plates are compatible with standard multichannel pipettes (both 8- and 16-channel).
Four 24-well / 96-well Piko PCR plates

Four 24-well / 96-well Piko PCR plates are equivalent to a standard SBS 96-well / 384-well plate, respectively.