

Portable Field PCR System
便携式现场 PCR 仪
- SKU PCR-0005
- PCR
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IEC 61010-1 test report (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Block format | 8-32 x 0.2 mL tubes |
|---|---|
| Temperature range | 4-99 °C |
| Maximum ramp rate | 2-4 °C per second |
| Temperature uniformity | ±0.4-0.5 °C |
| Optical channels | 0-4 depending on model |
| Run time | 40-90 min for 40 cycles |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 13485 manufacturing, MIQE guidelines, CLSI MM03-A2
What is the Portable Field PCR System?
A compact, low-power thermal cycler or real-time instrument with a small block, rugged case and battery or 12 V supply. It supports disease testing at farms, borders, outbreak sites and remote mobile laboratories.
What is the Portable Field PCR System?
A compact, low-power thermal cycler or real-time instrument with a small block, rugged case and battery or 12 V supply. It supports disease testing at farms, borders, outbreak sites and remote mobile laboratories.
Overview
The portable PCR system reduces the block to 8 to 32 tubes of 0.2 mL, cuts power draw to 50 to 150 W and encloses the optics or block in a shock-resistant case. Battery packs or 12 V vehicle supply allow operation where mains power is absent, and some models accept a solar charge controller. Real-time versions carry two to four optical channels; endpoint versions hold the product for later analysis. Cycle times of 40 to 90 minutes are typical, and the heated lid is usually fixed rather than adjustable. Ambient temperature tolerance is wider than in benchtop instruments, but accuracy still depends on stable power and a level surface. Field protocols usually combine a portable extraction method with lyophilised reagents and a cold-chain plan for controls.
How does it work?
PCR copies a target sequence with a thermostable DNA polymerase such as Taq, two primers that flank the target, deoxynucleoside triphosphates and a buffer. A thermal block cycles the reaction from about 95 °C, where double-stranded DNA separates, to 50 to 65 °C for primer annealing, then 72 °C for extension. Repeating 25 to 45 cycles doubles the product each round, so amplification is exponential while reagents last. Endpoint cyclers read the product afterwards on a gel or capillary system, while real-time instruments measure fluorescence each cycle using an intercalating dye or a hydrolysis probe, and the cycle threshold reflects the starting template amount. Quantitative results need a standard curve or reference gene, and melting curve analysis checks product specificity or detects sequence variants by high-resolution melting. Reverse transcription adds a step for RNA targets.
What are the key features?
- Block for 8 to 32 tubes of 0.2 mL.
- Power draw of 50 to 150 W with battery or 12 V supply.
- Shock-resistant case for transport in vehicles.
- Two to four optical channels in real-time versions.
- Wide ambient temperature tolerance.
- Compatible with lyophilised field reagents.
What are the technical specifications?
A typical portable field pcr system configuration offers block format of 8-32 x 0.2 mL tubes, temperature range of 4-99 °C, maximum ramp rate of 2-4 °C per second, temperature uniformity of ±0.4-0.5 °C, optical channels of 0-4 depending on model and run time of 40-90 min for 40 cycles. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Portable Field PCR System is used in field pathogen detection in agriculture, border and quarantine screening, outbreak investigation in remote areas and mobile veterinary diagnostics. Across the wider PCR class, laboratories also deploy it for gene expression analysis and transcript quantification, pathogen detection in clinical and food samples and genotyping and mutation screening.
Which standards and certifications apply?
Relevant standards and methods include ISO 13485 manufacturing, MIQE guidelines, CLSI MM03-A2, CLSI MM06-A2, IEC 61010-1 and IVDR (EU) 2017/746. Certification candidates for this model are CE, ISO 9001 manufacturing and IEC 61010-1 test report; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Keep pre-amplification and post-amplification work in separate areas with dedicated pipettes and filter tips, because carryover of amplicon is the main cause of false positives. Clean surfaces and equipment with fresh hypochlorite or a validated decontaminant, use UV where available and change gloves often. Calibrate block temperature and optical channels annually with a reference thermometer and dye plate, and check uniformity across the block. Verify performance with positive and negative controls and a standard curve in every run, and record Ct, efficiency and melt temperatures. Store primers and probes in small aliquots at the recommended temperature to avoid repeated freeze-thaw cycles, and protect fluorescent probes from light.
How do I select the right Portable Field PCR System?
Select this variant when testing must happen at the sampling site and sample transport is the limiting factor. Check block capacity against daily sample numbers, battery runtime for your test protocol, and whether real-time optics are needed for quantification. Confirm ambient temperature tolerance, reagent storage requirements and how the instrument is validated after transport or repeated field use.
How does it compare with other PCR variants?
Decide first whether you need qualitative detection, relative or absolute quantification, or sequence variant discrimination, because that separates endpoint cyclers from real-time and melt systems. Next, set the number of optical channels, since multiplex panels need two to six channels and matching filter sets. Throughput follows the plate format: 96 wells suits most laboratories, while 384-well plates and automation fit high-volume screening. Check block type, maximum ramp rate, temperature uniformity and gradient capability, which help with new primer sets. For field work, consider size, power options and tolerance of ambient temperature. Confirm analysis software, export formats, primer and probe support, and the validation documentation your quality system requires.
Full specifications
| Block format | 8-32 x 0.2 mL tubes |
|---|---|
| Temperature range | 4-99 °C |
| Maximum ramp rate | 2-4 °C per second |
| Temperature uniformity | ±0.4-0.5 °C |
| Optical channels | 0-4 depending on model |
| Run time | 40-90 min for 40 cycles |
| Power supply | 12 V DC or 100-240 V adapter, 50-150 W |
| Battery runtime | 4-8 h or 6-12 runs |
| Operating temperature | 5-40 °C ambient |
| Net weight | 2-6 kg with case |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Field pathogen detection in agriculture
- Border and quarantine screening
- Outbreak investigation in remote areas
- Mobile veterinary diagnostics
Key features
- Block for 8 to 32 tubes of 0.2 mL.
- Power draw of 50 to 150 W with battery or 12 V supply.
- Shock-resistant case for transport in vehicles.
- Two to four optical channels in real-time versions.
- Wide ambient temperature tolerance.
- Compatible with lyophilised field reagents.
Frequently asked questions about Portable Field PCR System
It can, if both are validated for the assay and the ambient conditions are controlled. Smaller blocks warm and cool faster with less uniformity, so confirm replicate agreement during field validation rather than assuming equivalence.
Most workflows use lyophilised or room-temperature-stable master mixes, with positive controls kept cold in a small cooler or cold box. Record temperature exposure for controls and replace any that exceeded the stated limits.
Throughput and automation. A portable unit processes 8 to 32 samples per run with manual setup, so it suits tens of samples per day rather than hundreds, and it still depends on a validated extraction method upstream.
Endpoint PCR amplifies the target and the product is analysed afterwards, usually by gel electrophoresis. Real-time PCR measures fluorescence during each cycle, which gives quantitative data, a cycle threshold value and a melting curve without opening the tube.
Most protocols use 25 to 45 cycles. Fewer cycles are used for abundant targets or quantitative work, while more may be needed for low-copy templates. Excess cycles increase non-specific products and background fluorescence.
Wells at different temperatures amplify at different rates, which shifts cycle threshold values between replicates. Uniformity within about ±0.3 to 0.5 °C across the block keeps replicates comparable and improves quantitative accuracy.
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