
Automated Agarose Gel Electrophoresis System with On-Board Imaging
带机上成像的自动琼脂糖凝胶电泳系统
- CE (to be confirmed)
- +2
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多通道琼脂糖凝胶电泳系统
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
| Number of sections | 2-4 independent sub-cells |
|---|---|
| Well capacity | 24-96 wells total |
| Gel size | 7 cm × 10 cm to 15 cm × 20 cm |
| Voltage range | 10-300 V, separately controlled |
| Buffer volume | 300-1,000 mL |
| Comb options | 0.75, 1.0, 1.5 mm thick, 8-20 teeth |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61010-2-081, IEC 61326-1
A horizontal tank with multiple independent lanes, trays or sub-cells, letting several users or protocols run at the same time. It keeps equipment cost low while handling moderate screening workloads in shared laboratories.
A horizontal tank with multiple independent lanes, trays or sub-cells, letting several users or protocols run at the same time. It keeps equipment cost low while handling moderate screening workloads in shared laboratories.
The multi-channel tank divides one buffer chamber into two to four sub-cells or provides multiple parallel trays with independent electrode pairs. Each section can run at its own voltage when separate leads are used, so a 20-minute PCR check and a 90-minute digest analysis can proceed in parallel. Total well capacity ranges from 24 to 96 wells across the sections, and gel trays are usually UV-transparent acrylic with fixed comb positions and casting gates. Buffer volume of 300 to 1,000 mL is common, and cooling is passive unless a recirculation port is fitted. Multichannel pipettes can load a full row at once, which reduces handling time. The design suits shared laboratories where several small runs happen during a day, and it costs less than an automated system.
In electrophoresis, an electric field drives charged molecules through a gel matrix: nucleic acids carry a negative charge from their phosphate backbone and migrate toward the anode, while their size and conformation determine how quickly they pass through the pores. Agarose gels of 0.5 to 2 percent resolve fragments from about 100 bp to 20 kb, and a buffer such as TAE or TBE carries the current between electrodes. Voltage is set per centimetre of gel length, commonly 5 to 10 V/cm, because higher voltages accelerate runs but heat the gel and blur bands. Sample loading dye adds density and tracking dyes, and a size marker gives fragment lengths by comparison. Detection uses intercalating stains under UV or blue light, or fluorescent labels in chip systems. Denaturing urea-PAGE resolves single-base differences in short oligonucleotides.
A typical multi-channel agarose gel electrophoresis system configuration offers number of sections of 2-4 independent sub-cells, well capacity of 24-96 wells total, gel size of 7 cm × 10 cm to 15 cm × 20 cm, voltage range of 10-300 V, separately controlled, buffer volume of 300-1,000 mL and comb options of 0.75, 1.0, 1.5 mm thick, 8-20 teeth. 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.
The Multi-Channel Agarose Gel Electrophoresis System is used in parallel PCR product checks, restriction digest analysis by several users, teaching laboratories with multiple groups and routine fragment screening. Across the wider Electrophoresis class, laboratories also deploy it for PCR product verification, DNA fragment sizing and restriction mapping and next-generation sequencing library quality control.
Relevant standards and methods include IEC 61010-1, IEC 61010-2-081, IEC 61326-1, ISO 13485 manufacturing and CLSI MM13-A. 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.
Prepare gels in a dedicated area and pour them on a level surface. Use fresh buffer at the recommended dilution, since reused buffer changes pH and conductivity, and check that electrode wires and connectors are clean. Keep the tank covered during runs to limit evaporation and protect operators from UV or electrical hazards, and never touch buffer or electrodes while a run is active. Choose low-toxicity stains where possible and follow local disposal rules for ethidium bromide or other intercalating agents. Clean and rinse tanks after each run to remove residual stain and agarose. Verify power supply calibration and check for cracked gel trays, worn leads and loose lid interlocks at fixed intervals.
Select the multi-channel tank for shared laboratories with moderate daily throughput, where several short runs must happen in parallel. Compare section count, well capacity and maximum voltage, and confirm that the tank fits your largest gel format. Check comb options, whether the lid carries separate leads and if you need buffer recirculation.
Match the method to the molecule and the resolution needed. Agarose in a horizontal tank is standard for double-stranded DNA fragments and PCR products, denaturing urea-PAGE for oligonucleotides and single-stranded fragments, and sieving-polymer chip systems for accurate sizing and quantification of many samples. Throughput then decides between manual tanks, multi-channel units and automated systems that combine running and imaging. Consider gel format and well count, buffer volume and cooling, and the detection method, because stains, UV exposure and fluorescence optics differ in sensitivity and safety. For power supplies, check voltage, current and power limits, programmability, and whether constant voltage, constant current or constant power modes are available.
| Number of sections | 2-4 independent sub-cells |
|---|---|
| Well capacity | 24-96 wells total |
| Gel size | 7 cm × 10 cm to 15 cm × 20 cm |
| Voltage range | 10-300 V, separately controlled |
| Buffer volume | 300-1,000 mL |
| Comb options | 0.75, 1.0, 1.5 mm thick, 8-20 teeth |
| Tray material | UV-transparent acrylic |
| Cooling | Passive, recirculation port optional |
| Typical run time | 20-90 min |
| Electrode material | Platinum wire |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Only if each has its own electrode pair and lead, and the buffer volumes are separated or the shared buffer does not create a current path between sections. Confirm bath separation before running two protocols at once.
Yes, if the comb spacing matches the pipette pitch, usually 9 mm for standard 8-channel pipettes. This reduces loading time considerably when a full row of samples is applied.
It helps for runs longer than about an hour or at high voltage, because it equalises pH and temperature between the electrode chambers. Short screening runs usually need no recirculation.
Use 0.7 to 1.0 percent agarose for fragments of 1 to 10 kb, 1.2 to 1.5 percent for 200 to 1,000 bp, and 2 percent for fragments under 200 bp. Higher percentages resolve small fragments but slow the run and reduce separation of large ones.
Common causes are excessive voltage that heats the gel, overloaded wells, degraded samples, or expired buffer with the wrong pH. Reduce voltage to 5 to 8 V/cm, load less sample and use fresh buffer to recover sharp bands.
Constant voltage gives reproducible band positions because migration depends mainly on voltage per centimetre. Constant current keeps heating more predictable during long runs, but voltage rises as buffer conductivity changes, so band positions can shift.

带机上成像的自动琼脂糖凝胶电泳系统




