

Portable Real-Time PCR Analyzer
便携式实时荧光定量 PCR 分析仪
- SKU MOA-0004
- Molecular Analysis
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- IP rating test report (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Sample capacity | 4–16 wells |
|---|---|
| Reaction volume | 10–25 μL |
| Temperature range | 35–99 °C |
| Maximum ramp rate | up to 5–8 °C/s |
| Fluorescence channels | 1–4 |
| Run time (40 cycles) | approx. 30–50 min |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61010-2-010, IEC 61010-2-101
What is the Portable Real-Time PCR Analyzer?
A portable real-time PCR analyzer is a compact, battery-capable instrument that runs 4 to 16 reactions with fluorescence detection, suitable for field sites and point-of-need testing. It is used for on-site pathogen screening, food safety checks and outbreak response where samples cannot easily reach a central laboratory.
What is the Portable Real-Time PCR Analyzer?
A portable real-time PCR analyzer is a compact, battery-capable instrument that runs 4 to 16 reactions with fluorescence detection, suitable for field sites and point-of-need testing. It is used for on-site pathogen screening, food safety checks and outbreak response where samples cannot easily reach a central laboratory.
Overview
Portable analyzers use a small Peltier or resistive heating block and compact optics, typically one to four fluorescence channels, in a rugged housing weighing 2 to 5 kg. Rapid thermal cycling, often with ramp rates above 5 °C per second, allows 40 cycles in around 30 to 50 minutes. They are commonly paired with lyophilized, room-temperature-stable reagent beads and pre-validated assay kits, reducing cold chain needs. Battery operation or 12 V vehicle power and tablet or touchscreen control enable use outside the laboratory. Because throughput is low, each run suits a limited number of samples. Sample preparation remains a constraint, so simple extraction kits or direct amplification protocols are usually paired. Environmental protection, such as IP-rated housings, dust resistance and shock tolerance, should be specified for field use.
How does it work?
Molecular analysis instruments amplify a nucleic acid target and monitor the reaction through fluorescence. In real-time PCR, a thermal block cycles between denaturation, annealing and extension, and optics read intercalating dyes such as SYBR Green or hydrolysis probes such as TaqMan at each cycle. The cycle at which fluorescence crosses a threshold, the quantification cycle (Cq), is inversely related to starting copy number, and a standard curve or comparative method gives relative or absolute quantity. Digital PCR partitions the reaction into thousands of nanoliter droplets or wells, amplifies each independently, and counts positive partitions; Poisson statistics then yield absolute copy number without calibration curves. Isothermal methods such as LAMP amplify at a constant temperature and detect fluorescence or turbidity. Melt-curve analysis verifies product specificity.
What are the key features?
- Compact housing of 2 to 5 kg for field transport.
- Battery or 12 V vehicle power operation.
- Fast thermal cycling completes 40 cycles in about 30 to 50 minutes.
- One to four fluorescence channels for multiplex detection.
- Compatible with lyophilized reagent beads to simplify cold chain.
- Touchscreen or tablet control with on-board analysis and report export.
What are the technical specifications?
A typical portable real-time pcr analyzer configuration offers sample capacity of 4–16 wells, reaction volume of 10–25 μL, temperature range of 35–99 °C, maximum ramp rate of up to 5–8 °C/s, fluorescence channels of 1–4 and run time (40 cycles) of approx. 30–50 min. 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 Real-Time PCR Analyzer is used in on-site pathogen screening, food and water safety spot checks, veterinary and agricultural disease surveillance and outbreak response and field research. Across the wider Molecular Analysis class, laboratories also deploy it for gene expression analysis, pathogen detection assay development and viral vector and residual DNA quantification.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61010-2-010, IEC 61010-2-101, IEC 61326-2-6, ISO 20395, ISO 22174 and MIQE guidelines. Certification candidates for this model are CE, ISO 9001 manufacturing and IP rating test report; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Molecular instruments require careful contamination control: separate pre- and post-amplification areas, use filter tips and include no-template controls. Thermal block temperature accuracy and uniformity should be verified periodically with a calibrated temperature probe, and optical calibration with dye plates should be performed after installation and at intervals recommended by the manufacturer. Keep the instrument on a stable bench with adequate ventilation, and protect lamps or LEDs from unnecessary exposure. Follow MIQE guidance when reporting qPCR data, and keep raw fluorescence data archived. Regulated laboratories should confirm software access control and audit trail.
How do I select the right Portable Real-Time PCR Analyzer?
Choose a portable analyzer when testing must be done at the sampling site with few samples per run. Specify channels, battery life, environmental protection, reagent format and connectivity. For more than about 16 samples per run or validated laboratory workflows, a 96-well benchtop system is more suitable.
How does it compare with other Molecular Analysis variants?
Decide first between relative quantification, for which real-time PCR is usually sufficient, and absolute quantification of rare targets or small fold changes, for which digital PCR offers better precision. Match well format to throughput: 96-well suits routine work, and 384-well suits screening. Count optical channels against multiplex needs, since four to six channels are common for multiplex panels. Consider ramp rate and run time, block uniformity and lid heating for reproducibility. For field or point-of-need testing, portable analyzers with battery operation and lyophilized reagents are appropriate. Check reagent openness, software features for analysis and export, and whether the instrument can support the validation documents that regulated workflows require.
Full specifications
| Sample capacity | 4–16 wells |
|---|---|
| Reaction volume | 10–25 μL |
| Temperature range | 35–99 °C |
| Maximum ramp rate | up to 5–8 °C/s |
| Fluorescence channels | 1–4 |
| Run time (40 cycles) | approx. 30–50 min |
| Weight | 2–5 kg |
| Battery run time | approx. 3–4 h (typical) |
| Operating temperature | 5–40 °C |
| Connectivity | USB, Wi-Fi, Bluetooth |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- On-site pathogen screening
- Food and water safety spot checks
- Veterinary and agricultural disease surveillance
- Outbreak response and field research
Key features
- Compact housing of 2 to 5 kg for field transport.
- Battery or 12 V vehicle power operation.
- Fast thermal cycling completes 40 cycles in about 30 to 50 minutes.
- One to four fluorescence channels for multiplex detection.
- Compatible with lyophilized reagent beads to simplify cold chain.
- Touchscreen or tablet control with on-board analysis and report export.
Frequently asked questions about Portable Real-Time PCR Analyzer
Performance depends on thermal accuracy, optical sensitivity and assay quality. Properly validated portable analyzers can produce Cq values comparable to benchtop units, but throughput, channel count and uniformity are typically lower. Verify with side-by-side testing of your assay.
Rapid extraction methods such as magnetic bead kits with hand-operated tools, simple lysis buffers and direct-amplification reagents reduce equipment needs. Extraction efficiency and inhibitor removal should be validated for the matrix, such as soil, food or swabs.
Use the manufacturer case, protect from shocks, moisture and temperatures beyond the specified operating range, and allow the instrument to acclimate before use to avoid condensation. Run a verification check after long transport or exposure to extreme conditions.
It measures the amount of a specific DNA or RNA sequence in a sample by amplifying it and monitoring fluorescence. Results are reported as Cq values, relative expression, absolute copy number or presence/absence of a pathogen or genetic variant.
Use digital PCR when you need absolute copy number without standards, detection of rare variants below about 0.1 percent allele fraction, or small fold-change differences such as copy number variation. qPCR remains faster and cheaper for routine relative quantification and high-throughput screening.
The quantification cycle (Cq), also called Ct, is the PCR cycle at which fluorescence first rises above a set threshold. Lower Cq means more starting template, and each cycle difference corresponds to about a twofold change when amplification efficiency is near 100 percent.





