

Automated PCR Setup Workstation
自动化 PCR 配制工作站
- SKU PCW-0004
- PCR Workstations
- 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
| Plate formats | 96- and 384-well PCR plates |
|---|---|
| Pipetting volume range | 0.5–1000 µL |
| Pipetting accuracy | ±2% at 10 µL |
| Pipetting precision (CV) | < 2% at 10 µL |
| Set-up time, 96-well plate | 10–20 min |
| Enclosure airflow | HEPA downflow, ISO Class 5 |
By Lab Manufacturers China Technical TeamLast reviewed Standards: EN 12469, NSF/ANSI 49, ISO 14644-1
What is the Automated PCR Setup Workstation?
An automated PCR setup workstation uses a pipetting robot inside a HEPA- and UV-equipped enclosure to dispense master mix and template into PCR plates, typically 96 or 384 wells. It is the right choice for laboratories that need reproducible, traceable plate set-up at volumes above a few dozen reactions per day.
What is the Automated PCR Setup Workstation?
An automated PCR setup workstation uses a pipetting robot inside a HEPA- and UV-equipped enclosure to dispense master mix and template into PCR plates, typically 96 or 384 wells. It is the right choice for laboratories that need reproducible, traceable plate set-up at volumes above a few dozen reactions per day.
Overview
The workstation combines a multi-channel pipetting arm, a deck for tips, reagent racks, sample tubes and plates, and an enclosure with HEPA downflow and UV lamps. Software defines the plate layout, master-mix preparation and sample transfer, with barcode reading for samples and plates. Pipetting accuracy is typically ±2% at 10 µL and CV below 2%, and volumes from 0.5 to 1000 µL are supported with interchangeable tips. Liquid-level detection, clot detection and cold blocks for reagents are usual options. A 96-well plate can be set up in 10–20 minutes. Automated set-up reduces manual variability, contamination risk and repetitive strain. Validation of pipetting performance with gravimetric or photometric tests should be done at installation.
How does it work?
PCR contamination arises mainly from amplicons carried over from previous reactions and from ambient DNA. A PCR workstation reduces this risk with three mechanisms. First, an enclosed or laminar-flow workspace limits airborne particles: HEPA filters remove at least 99.99% of particles at 0.3 µm, and airflow passes in a controlled direction over the work surface. Second, ultraviolet light at 254 nm crosslinks DNA on surfaces and in air inside the cabinet, destroying residual template. Third, smooth stainless steel or epoxy surfaces allow chemical cleaning with bleach or DNA-decontaminating reagents. Some systems add a door interlock so UV cannot run when the sash is open, and timers for automatic UV cycles.
What are the key features?
- Multi-channel pipetting arm with interchangeable tips
- HEPA downflow and UV decontamination in the enclosure
- Liquid-level and clot detection for reliable dispensing
- Barcode reading of samples and plates
- Cooled reagent blocks at 4–10 °C
- LIMS export of plate maps and run logs
What are the technical specifications?
A typical automated pcr setup workstation configuration offers plate formats of 96- and 384-well PCR plates, pipetting volume range of 0.5–1000 µL, pipetting accuracy of ±2% at 10 µL, pipetting precision (CV) of < 2% at 10 µL, set-up time, 96-well plate of 10–20 min and enclosure airflow of HEPA downflow, ISO Class 5. 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 Automated PCR Setup Workstation is used in high-volume diagnostic plate set-up, genotyping plate preparation, reference laboratory workflows and research screening assays. Across the wider PCR Workstations class, laboratories also deploy it for pre-PCR reagent and sample set-up, forensic DNA analysis and molecular diagnostics.
Which standards and certifications apply?
Relevant standards and methods include EN 12469, NSF/ANSI 49, ISO 14644-1, EN 1822 (HEPA filters), IEC 61010-1, IEC 61010-2-101 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.
Place the workstation in a low-traffic area of the pre-amplification room, away from doors and air vents. Clean surfaces before and after use with 10% bleach followed by water or 70% ethanol, and run the UV cycle, typically 15–30 minutes, before work. UV lamps lose output with age, so record hours and replace them at the manufacturer's interval, usually 6,000–9,000 hours. Test HEPA filter integrity and airflow velocity at installation and annually, or as required by the standard applied. Keep pipettes, tips and racks dedicated to the workstation, and never bring amplified product or post-PCR equipment into the pre-PCR area.
How do I select the right Automated PCR Setup Workstation?
Select an automated set-up workstation when plate count is high and reproducibility and traceability matter more than hardware cost. It needs validation, trained operators and service support. In an RFQ, specify plate formats, volume range, accuracy and CV at working volumes, enclosure class, barcode, LIMS interface, cooling, and qualification documents such as IQ/OQ.
How does it compare with other PCR Workstations variants?
Select by the level of protection needed. A UV dead-air cabinet protects reagents at low cost, a laminar-flow hood adds HEPA airflow for cleaner preparation, and a Class II cabinet also protects the operator when handling infectious samples. Check interior size against the racks, pipettes and centrifuge you need inside, and confirm UV lamp wavelength, timer and door interlock. Ductless carbon-filter units suit post-PCR work with volatile reagents. Automated set-up stations reduce manual variability and suit high volumes. Consider noise, vibration and lighting, and whether the workstation must be certified to a biosafety standard such as EN 12469 or NSF/ANSI 49.
Full specifications
| Plate formats | 96- and 384-well PCR plates |
|---|---|
| Pipetting volume range | 0.5–1000 µL |
| Pipetting accuracy | ±2% at 10 µL |
| Pipetting precision (CV) | < 2% at 10 µL |
| Set-up time, 96-well plate | 10–20 min |
| Enclosure airflow | HEPA downflow, ISO Class 5 |
| UV decontamination | 254 nm, programmable |
| Sample tracking | Barcode reader |
| Reagent cooling | 4–10 °C |
| Power supply | 100–240 V AC, 50/60 Hz, about 600 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-volume diagnostic plate set-up
- Genotyping plate preparation
- Reference laboratory workflows
- Research screening assays
Key features
- Multi-channel pipetting arm with interchangeable tips
- HEPA downflow and UV decontamination in the enclosure
- Liquid-level and clot detection for reliable dispensing
- Barcode reading of samples and plates
- Cooled reagent blocks at 4–10 °C
- LIMS export of plate maps and run logs
Frequently asked questions about Automated PCR Setup Workstation
Typical pipetting is within ±2% at 10 µL and CV below 2%, verified by gravimetric or dye-based tests. Actual values depend on liquid properties, tip type and calibration, so validate with your reagents.
Yes, by removing manual pipetting, using filtered tips, enclosing the deck under HEPA airflow and UV, and tracking samples by barcode. Good practice such as cleaning and no-template controls still applies.
Daily surface cleaning, periodic pipette-channel calibration, UV lamp replacement and annual HEPA checks. A preventive maintenance contract with documented service visits is recommended, especially for regulated work.
A PCR workstation provides a clean, often UV-decontaminated space for preparing PCR reactions. It protects reagents and template from airborne DNA and amplicons, which reduces false-positive results in diagnostic, forensic and research amplification work.
It is not always required. A UV dead-air cabinet may suffice for routine work, but HEPA laminar flow gives a cleaner environment and is preferred for trace DNA, forensic and clinical diagnostics where contamination risk must be minimised.
Typical decontamination cycles are 15–30 minutes before work. Effectiveness depends on lamp age, distance to surfaces and shading, so follow supplier guidance and replace lamps at the recommended hour count.
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