

Wet Tank Electroblotting System
湿转式电转印槽
- SKU BLS-0001
- 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 area (W x L) | approx. 10 x 7.5 cm (mini) or 15 x 15 cm (midi) |
|---|---|
| Gels per run | 1–2 (up to 4 in large tanks) |
| Buffer volume | 1–4 L |
| Typical transfer conditions | 100 V, 350 mA for 1–2 h; 20–30 V overnight |
| Maximum voltage | 200 V DC |
| Maximum current | 1.5 A |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61326-1, ISO 17025
What is the Wet Tank Electroblotting System?
A buffer-filled tank that holds gel-membrane cassettes between plate or wire electrodes with a cooling core. It gives efficient and forgiving transfer of proteins across a wide size range, especially large proteins above 100 kDa.
What is the Wet Tank Electroblotting System?
A buffer-filled tank that holds gel-membrane cassettes between plate or wire electrodes with a cooling core. It gives efficient and forgiving transfer of proteins across a wide size range, especially large proteins above 100 kDa.
Overview
The wet tank system is the classic protein electroblotting format. Gel and membrane sandwiches are clamped in rigid cassettes with sponges and filter paper and submerged in a tank containing 1–4 L of transfer buffer, usually Towbin buffer with methanol. Electrodes of platinum wire or stainless-steel plate on either side give a uniform field. A frozen cooling unit or a circulating coil absorbs Joule heat, and a stir bar keeps buffer homogeneous. Transfers run at 100 V for 1–2 hours, or at 20–30 V overnight at cold temperature for large proteins. Because the sandwich is fully immersed, the format tolerates small variations in assembly and is the preferred method for quantitative blots and for proteins above 100 kDa. The drawback is larger buffer volume and longer run time.
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?
- Fully immersed transfer sandwich tolerates small assembly differences and supports large proteins
- Frozen cooling core or circulating coil absorbs heat during long high-current transfers
- Stir bar keeps buffer homogeneous so the field stays uniform across the tank
- Rigid cassettes hold one or two gels per tank with color-coded sides for orientation
- Platinum or stainless-steel electrodes with shrouded leads ensure corrosion-resistant contact
- Compatible with mini and midi gel formats through interchangeable cassettes
What are the technical specifications?
A typical wet tank electroblotting system configuration offers transfer area (W x L) of approx. 10 x 7.5 cm (mini) or 15 x 15 cm (midi), gels per run of 1–2 (up to 4 in large tanks), buffer volume of 1–4 L, typical transfer conditions of 100 V, 350 mA for 1–2 h; 20–30 V overnight, maximum voltage of 200 V DC and maximum current of 1.5 A. 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 Wet Tank Electroblotting System is used in quantitative western blotting, large protein transfer above 100 kDa, overnight low-voltage transfer and routine immunodetection. 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 Wet Tank Electroblotting System?
Select wet tank transfer for large proteins, quantitative blots or where consistency matters more than speed. It uses more buffer and takes longer than semi-dry or rapid systems. Specify gel format, number of cassettes, cooling method, maximum current and membrane size, and confirm the power supply can deliver the current.
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 area (W x L) | approx. 10 x 7.5 cm (mini) or 15 x 15 cm (midi) |
|---|---|
| Gels per run | 1–2 (up to 4 in large tanks) |
| Buffer volume | 1–4 L |
| Typical transfer conditions | 100 V, 350 mA for 1–2 h; 20–30 V overnight |
| Maximum voltage | 200 V DC |
| Maximum current | 1.5 A |
| Cooling method | Frozen cooling unit or circulating coil |
| Electrode material | Platinum wire or stainless steel |
| Protein size range | approx. 10–250 kDa |
| Tank material | Polycarbonate |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Quantitative western blotting
- Large protein transfer above 100 kDa
- Overnight low-voltage transfer
- Routine immunodetection
Key features
- Fully immersed transfer sandwich tolerates small assembly differences and supports large proteins
- Frozen cooling core or circulating coil absorbs heat during long high-current transfers
- Stir bar keeps buffer homogeneous so the field stays uniform across the tank
- Rigid cassettes hold one or two gels per tank with color-coded sides for orientation
- Platinum or stainless-steel electrodes with shrouded leads ensure corrosion-resistant contact
- Compatible with mini and midi gel formats through interchangeable cassettes
Frequently asked questions about Wet Tank Electroblotting System
Large proteins migrate slowly out of the gel and need longer transfer times with sufficient buffer and cooling. The immersed sandwich and cooling core of a wet tank allow extended or overnight runs without drying or overheating.
Methanol helps strip SDS from proteins and improves their binding to nitrocellulose or PVDF, usually at 10–20%. It can reduce transfer of very large proteins, so lowering methanol and adding a small amount of SDS can help for proteins above 100 kDa.
Use the frozen cooling unit, run the tank in a cold room or on ice, stir the buffer, and keep buffer cold before use. Reduce current or voltage for long runs, since excessive heat can cause band distortion and buffer evaporation.
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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