

384-Well Thermal Cycler
384 孔热循环仪
- SKU COP-0004
- 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 | 1 × 384-well plate |
|---|---|
| Temperature range | 4–99 °C |
| Max block ramp rate | 2–3 °C/s |
| Block uniformity | ±0.4 °C |
| Temperature accuracy | ±0.25 °C |
| Reaction volume | 3–20 µL |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 20395, ISO 22174, IEC 61010-1
What is the 384-Well Thermal Cycler?
A 384-well thermal cycler holds a 384-well plate in one block, typically with reaction volumes of 5–20 µL, to multiply throughput and cut reagent use per reaction. It is the right choice for high-throughput genotyping and screening laboratories that use automated liquid handlers.
What is the 384-Well Thermal Cycler?
A 384-well thermal cycler holds a 384-well plate in one block, typically with reaction volumes of 5–20 µL, to multiply throughput and cut reagent use per reaction. It is the right choice for high-throughput genotyping and screening laboratories that use automated liquid handlers.
Overview
The 384-well cycler uses a larger Peltier block with many thermoelectric modules to maintain uniformity across the full plate, including corner and edge wells that are most prone to drift. Ramp rates are typically 1.5–3 °C/s because of the higher thermal mass. Block uniformity of ±0.4 °C and accuracy of ±0.25 °C are typical. A motorized heated lid with higher compression force is needed to seal small wells. Reaction volumes of 3–20 µL require precise dispensing, so the cycler is normally paired with a liquid handler and plate sealer. Plate-based barcode input and software integration with robotic systems are common options. Edge evaporation should be checked in validation runs, especially for low-volume assays.
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?
- 384-well block supports 3–20 µL reactions to reduce reagent use
- High-force motorized lid seals low-volume wells reliably
- Edge and corner well compensation for uniform performance
- Compatible with robotic plate loaders on selected models
- Barcode reader option for plate tracking
- Optional 96-well adapter block for flexibility
What are the technical specifications?
A typical 384-well thermal cycler configuration offers block format of 1 × 384-well plate, temperature range of 4–99 °C, max block ramp rate of 2–3 °C/s, block uniformity of ±0.4 °C, temperature accuracy of ±0.25 °C and reaction volume of 3–20 µL. 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 384-Well Thermal Cycler is used in high-throughput SNP genotyping, compound and library screening, automated sequencing template preparation and biobank sample processing. 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 384-Well Thermal Cycler?
Select a 384-well cycler if you process hundreds of samples per run with a liquid handler, and you can validate low-volume chemistry. It needs more bench space and precise dispensing versus 96-well units. In an RFQ, specify plate type and skirt, uniformity including corner wells, lid force, automation interface, barcode needs, reaction volume range and whether a 96-well adapter is required.
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 | 1 × 384-well plate |
|---|---|
| Temperature range | 4–99 °C |
| Max block ramp rate | 2–3 °C/s |
| Block uniformity | ±0.4 °C |
| Temperature accuracy | ±0.25 °C |
| Reaction volume | 3–20 µL |
| Heated lid range | 30–110 °C |
| Typical 30-cycle run time | 1.5–2.5 h |
| Interfaces | USB, Ethernet, optional barcode reader |
| 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
- High-throughput SNP genotyping
- Compound and library screening
- Automated sequencing template preparation
- Biobank sample processing
Key features
- 384-well block supports 3–20 µL reactions to reduce reagent use
- High-force motorized lid seals low-volume wells reliably
- Edge and corner well compensation for uniform performance
- Compatible with robotic plate loaders on selected models
- Barcode reader option for plate tracking
- Optional 96-well adapter block for flexibility
Frequently asked questions about 384-Well Thermal Cycler
Not without an adapter. The 384-well block has a different well pitch, so a dedicated 96-well adapter insert or a separate block is required. Check whether the selected model offers this option.
Edge and corner wells lose heat faster and are more prone to evaporation, which concentrates the reaction. A high-force heated lid, good seal film, and uniformity verification across all wells reduce the effect.
Many 384-well cyclers offer a motorized lid and software interface for robotic plate handling. Confirm the communication protocol, plate gripper height and lid open position with the automation supplier before purchase.
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.
Related models





