

Dual-Block Thermal Cycler
双模块热循环仪
- SKU COP-0002
- Conventional PCR
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Block format | 2 × 48 or 2 × 96 wells (0.2 mL) |
|---|---|
| Temperature range | 4–99 °C |
| Max block ramp rate | 2.5–3.5 °C/s |
| Block uniformity | ±0.3 °C |
| Temperature accuracy | ±0.25 °C |
| Independent blocks | 2 |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 20395, ISO 22174, IEC 61010-1
What is the Dual-Block Thermal Cycler?
A dual-block thermal cycler contains two independently controlled blocks, usually 48 wells each or two 96-well blocks, so two different PCR programs run at the same time. It is the right choice for shared laboratories or workflows that need different annealing temperatures or cycle counts without waiting for a single block to finish.
What is the Dual-Block Thermal Cycler?
A dual-block thermal cycler contains two independently controlled blocks, usually 48 wells each or two 96-well blocks, so two different PCR programs run at the same time. It is the right choice for shared laboratories or workflows that need different annealing temperatures or cycle counts without waiting for a single block to finish.
Overview
A dual-block cycler pairs two Peltier blocks with individual heated lids and independent control electronics, so each block starts, pauses and stops its own protocol. Common formats are 2 × 48 wells or 2 × 96 wells. Performance per block is similar to a standard cycler, with ramp rates of 2–3.5 °C/s and uniformity near ±0.3 °C. Because both blocks can also run the same program, the instrument can be used as a single cycler with double capacity. Shared cores benefit because different users can work simultaneously, and method development benefits because two conditions can be compared in one session. Power draw and footprint are higher than a single-block unit, and each block requires its own calibration check.
How does it work?
A thermal cycler holds reaction tubes or plates in a metal block whose temperature is controlled by Peltier thermoelectric elements. Each cycle denatures double-stranded DNA at about 94–98 °C, cools to the primer annealing temperature, typically 50–68 °C, and then heats to about 72 °C so a thermostable DNA polymerase extends the primers. Repeating this 25–40 times amplifies the target exponentially. Key components include the Peltier-driven block, a heat sink and fan, a temperature sensor feedback loop, a heated lid that prevents condensation and evaporation, and a controller that stores multi-step programs. Block uniformity and ramp rate determine how reproducibly each well reaches its set temperature.
What are the key features?
- Two independently programmable blocks run different protocols at once
- Separate heated lids allow different tube heights on each block
- Blocks can be linked to run one program at double capacity
- Per-block gradient capability available on selected models
- Independent status display and alarms for each block
- Shared program library across both blocks
What are the technical specifications?
A typical dual-block thermal cycler configuration offers block format of 2 × 48 or 2 × 96 wells (0.2 mL), temperature range of 4–99 °C, max block ramp rate of 2.5–3.5 °C/s, block uniformity of ±0.3 °C, temperature accuracy of ±0.25 °C and independent blocks of 2. 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 Dual-Block Thermal Cycler is used in shared core facilities, PCR method development, parallel genotyping projects and multi-user teaching labs. Across the wider Conventional PCR class, laboratories also deploy it for gene cloning and plasmid construction, genotyping and mutation screening and pathogen detection by end-point PCR.
Which standards and certifications apply?
Relevant standards and methods include ISO 20395, ISO 22174, IEC 61010-1, IEC 61010-2-010, MIQE guidelines (research reporting) and CLSI MM19. Certification candidates for this model are CE and ISO 9001 manufacturing; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install the cycler on a stable bench with at least 10 cm of clearance for air intake and exhaust, away from direct sunlight and drafts. Verify block temperature accuracy and uniformity at installation and at least annually using a calibrated multi-point probe, and record results for audit. Clean the block wells with a lint-free swab and 70% ethanol to remove spilled reagent and prevent cross-contamination, and inspect the heated lid seal. Use sealing films or caps matched to the lid pressure. Keep pre-PCR and post-PCR work areas physically separated, and run no-template controls to detect amplicon carry-over. Firmware updates and program backups should be controlled under the laboratory's document system.
How do I select the right Dual-Block Thermal Cycler?
Select a dual-block cycler when two or more users share one instrument or when you often compare annealing conditions side by side. Compared with a single 96-well cycler, it costs more and uses more bench space, but it removes queueing. In an RFQ, specify wells per block, independent gradient needs, lid tube-height range, calibration requirement per block, and whether blocks can be linked for a single large run.
How does it compare with other Conventional PCR variants?
Choose first by throughput and format: 96-well blocks suit most research work, 384-well blocks suit high-throughput screening, and small 16–48 well units suit teaching or occasional use. Next, compare ramp rate and block uniformity, because fast cyclers shorten run time but need polymerases and buffers validated for short steps. Dual-block instruments allow two independent programs at once and help shared core facilities. Check the heated lid range, programmable features such as touchdown and gradient, and whether the block is interchangeable. Consider connectivity for audit trails if the laboratory works under quality systems, and confirm the tube or plate formats you use, including low-profile plates and strip tubes.
Full specifications
| Block format | 2 × 48 or 2 × 96 wells (0.2 mL) |
|---|---|
| Temperature range | 4–99 °C |
| Max block ramp rate | 2.5–3.5 °C/s |
| Block uniformity | ±0.3 °C |
| Temperature accuracy | ±0.25 °C |
| Independent blocks | 2 |
| Heated lid range | 30–110 °C |
| Reaction volume | 5–100 µL |
| Display | 7 in color touchscreen |
| Power supply | 100–240 V AC, 50/60 Hz, about 900 W |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Shared core facilities
- PCR method development
- Parallel genotyping projects
- Multi-user teaching labs
Key features
- Two independently programmable blocks run different protocols at once
- Separate heated lids allow different tube heights on each block
- Blocks can be linked to run one program at double capacity
- Per-block gradient capability available on selected models
- Independent status display and alarms for each block
- Shared program library across both blocks
Frequently asked questions about Dual-Block Thermal Cycler
Yes. Each block has its own controller, so one can be loaded and started while the other is mid-run or idle. Starting one protocol does not interrupt the other, though a power failure will affect both.
Per-block uniformity is typically comparable, around ±0.3 °C, but each block should be verified separately. Request calibration data for both blocks and check them during annual performance verification.
Yes, peak power is typically 800–1000 W versus about 600 W for a single block, since two Peltier assemblies can heat at once. Check the bench circuit rating and ventilation clearances at the planned location.
It amplifies a chosen DNA segment by cycling a reaction mix through denaturation, annealing and extension temperatures. The product is analysed after the run, usually on an agarose gel. Typical uses include cloning, genotyping, sequencing template preparation, and qualitative detection of pathogens or transgenes.
Conventional PCR reads the result at the end of the run, usually by gel electrophoresis, and gives a qualitative yes or no answer. Real-time PCR measures fluorescence every cycle and can quantify starting template. Conventional cyclers cost less and have no optical module.
Block temperature accuracy and uniformity should be verified at installation and at least once a year, or after any repair or relocation. Laboratories working under ISO 17025 or GMP often shorten this interval and keep calibration certificates traceable to national standards.
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