

Rapid High-Current Protein Transfer System
快速大电流蛋白转印系统
- SKU BLS-0003
- Blotting Systems
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- RoHS (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Transfer time | 3–10 min |
|---|---|
| Transfer area (W x L) | approx. 8.5 x 13.5 cm (mini/midi stacks) |
| Gels per run | 1–2 |
| Output current | up to 2.5 A |
| Output voltage | up to 25 V DC |
| Programs | Preset (low, mixed, high MW) plus user-defined |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61326-1, ISO 17025
What is the Rapid High-Current Protein Transfer System?
A cassette-based blotter that completes protein transfer in about 3–10 minutes using high current and ready-to-use transfer stacks. It is selected by laboratories with high sample turnover that want reproducible, hands-off blotting.
What is the Rapid High-Current Protein Transfer System?
A cassette-based blotter that completes protein transfer in about 3–10 minutes using high current and ready-to-use transfer stacks. It is selected by laboratories with high sample turnover that want reproducible, hands-off blotting.
Overview
Rapid transfer systems shorten western blotting by combining high-current power delivery with matched transfer stacks that include buffer, membrane and filter paper in pre-assembled form. The instrument houses a cassette in which the stack is placed, and a built-in power supply delivers a fixed high-current program, typically 1.3–2.5 A for 3–10 minutes. Because electrodes are integrated into the stack or cassette lid, contact is reproducible and operator variation is low. Programs are available for mixed, low, and high molecular weight proteins and for different gel formats, and some units also accept pre-cast mini and midi gels. Consumable stacks add per-run cost, and the format needs validation with your gel chemistry. Benefits include speed, consistent results, and minimal buffer handling, with no need for cooling or external power supply.
How does it work?
Blotting moves separated molecules from a fragile gel to a durable membrane while preserving their relative positions. In electroblotting, the gel and membrane are pressed together in a sandwich between filter papers and sponges or buffer-wetted stacks, and an electric field drives charged molecules out of the gel and onto the membrane, where they bind by hydrophobic or electrostatic interaction. Wet tank systems submerge the sandwich in buffer between plate electrodes, semi-dry systems place it between flat graphite or metal plate electrodes with only buffer-soaked paper, and rapid systems use high current with special buffers. Vacuum and capillary blotting draw buffer through the gel to carry nucleic acids onto the membrane. After transfer, the membrane is blocked and probed, and signals are detected chemically or by fluorescence.
What are the key features?
- Integrated power supply delivers 1.3–2.5 A programs completing transfer in 3–10 minutes
- Pre-assembled transfer stacks with buffer and membrane reduce set-up time and operator variation
- Preset programs cover low, mixed and high molecular weight proteins and mini or midi gels
- Integrated electrodes in the stack or lid give reproducible contact across the whole membrane
- Touch-screen or keypad interface stores custom methods and shows remaining time
- No external cooling or power supply is needed, which saves bench space
What are the technical specifications?
A typical rapid high-current protein transfer system configuration offers transfer time of 3–10 min, transfer area (W x L) of approx. 8.5 x 13.5 cm (mini/midi stacks), gels per run of 1–2, output current of up to 2.5 A, output voltage of up to 25 V DC and programs of Preset (low, mixed, high MW) plus user-defined. 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 Rapid High-Current Protein Transfer System is used in high-throughput western blotting, core facility protein analysis, quality control immunoassays and time-critical research workflows. Across the wider Blotting Systems class, laboratories also deploy it for western blotting, southern blotting and northern blotting.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61326-1, ISO 17025, Ph. Eur. 2.2.31 and USP <1053>. Certification candidates for this model are CE, ISO 9001 manufacturing and RoHS; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Good contact between gel and membrane without trapped bubbles is the main factor for transfer quality, so roll out air with a tube before closing the cassette. Pre-wet PVDF in methanol and equilibrate gels in transfer buffer. Keep buffer cold or use an ice pack and stirrer for wet transfers to limit heating. Do not exceed the current or voltage limits of the tank, and follow the orientation of electrodes carefully. Clean electrodes and cassettes regularly, and do not leave buffer in the tank. Mind methanol flammability and the chemical safety of acrylamide and probe reagents. Electrical safety follows IEC 61010-1, and transfer efficiency should be checked with reversible stains or pre-stained markers.
How do I select the right Rapid High-Current Protein Transfer System?
Select a rapid system when many blots are run each week and turnaround, consistency and reduced hands-on time justify per-run consumable cost. Specify transfer area, preset programs, membrane type, consumable stack supply and lead time, and pre-cast gel compatibility.
How does it compare with other Blotting Systems variants?
Choose the transfer format from the target and the workload. Wet tank transfer is the most forgiving for large proteins above 100 kDa and for quantitative work. Semi-dry is faster and uses less buffer, which suits routine transfers of small and medium proteins. Rapid systems finish in about 7–10 minutes and suit high sample turnover but need matching consumables. Vacuum and capillary blotting are standard for Southern and northern work with large DNA and RNA fragments. Dot or slot manifolds are used when no separation is needed. Check transfer area against your gel format, membrane compatibility with PVDF, nitrocellulose or nylon, cooling options, maximum current and whether the power supply you have can drive the system.
Full specifications
| Transfer time | 3–10 min |
|---|---|
| Transfer area (W x L) | approx. 8.5 x 13.5 cm (mini/midi stacks) |
| Gels per run | 1–2 |
| Output current | up to 2.5 A |
| Output voltage | up to 25 V DC |
| Programs | Preset (low, mixed, high MW) plus user-defined |
| Membrane compatibility | PVDF and nitrocellulose |
| Protein size range | approx. 10–250 kDa |
| Consumables | Matched transfer stacks |
| Power input | 100–240 V AC, 50/60 Hz |
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 western blotting
- Core facility protein analysis
- Quality control immunoassays
- Time-critical research workflows
Key features
- Integrated power supply delivers 1.3–2.5 A programs completing transfer in 3–10 minutes
- Pre-assembled transfer stacks with buffer and membrane reduce set-up time and operator variation
- Preset programs cover low, mixed and high molecular weight proteins and mini or midi gels
- Integrated electrodes in the stack or lid give reproducible contact across the whole membrane
- Touch-screen or keypad interface stores custom methods and shows remaining time
- No external cooling or power supply is needed, which saves bench space
Frequently asked questions about Rapid High-Current Protein Transfer System
With matched stacks and suitable programs, rapid transfer gives efficiency comparable to traditional methods for most proteins. Very large or very small proteins may need program adjustment, and results should be validated with your gels and antibodies.
Some instruments accept user-prepared stacks with a dedicated high-ionic-strength buffer, while others require supplier stacks. Check compatibility before purchase, since buffer composition affects conductivity, heating and the current the system delivers.
No, rapid systems normally include a built-in power supply matched to the cassette and program. This removes the need for a separate high-current supply and keeps settings consistent between operators.
A blotting system moves proteins, DNA or RNA from an electrophoresis gel onto a membrane while preserving their pattern, so they can be detected with antibodies or probes. It includes wet tank, semi-dry, rapid, vacuum and dot-blot devices.
Wet transfer submerges the gel-membrane sandwich in a buffer tank and is better for large proteins and quantitative work. Semi-dry uses only buffer-soaked paper between plate electrodes, so it is faster and uses less buffer but can be less efficient for large proteins.
PVDF binds more protein, withstands stripping and reprobing, and needs methanol pre-wetting. Nitrocellulose needs no activation and gives low background, so it suits routine immunodetection. Nylon is used for nucleic acids, which require crosslinking after transfer.
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