

Mini Vertical Gel Electrophoresis System for Proteins
蛋白质微型垂直凝胶电泳系统
- SKU VEE-0001
- Vertical Electrophoresis
- 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
| Gel size (W x L) | approx. 8 x 7 cm |
|---|---|
| Gel thickness options | 0.75, 1.0, 1.5 mm |
| Number of gels per run | 1–4 |
| Wells per comb | 10, 12, 15, 17 |
| Buffer volume | approx. 600–1000 mL total |
| Maximum voltage | 300 V DC |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61326-1, Ph. Eur. 2.2.31
What is the Mini Vertical Gel Electrophoresis System for Proteins?
A compact vertical unit for 8 x 7 cm polyacrylamide gels that runs one to four gels in 40–90 minutes. It is the standard choice for routine SDS-PAGE, purity checks and sample preparation before western blotting.
What is the Mini Vertical Gel Electrophoresis System for Proteins?
A compact vertical unit for 8 x 7 cm polyacrylamide gels that runs one to four gels in 40–90 minutes. It is the standard choice for routine SDS-PAGE, purity checks and sample preparation before western blotting.
Overview
The mini vertical system is the most widely used format in protein laboratories. A central core holds one or two gel cassettes, and the upper buffer chamber is formed between the core and the plates, so a small volume of about 100–200 mL of buffer in the outer tank is enough. Glass plates of roughly 10 x 10 cm and a short plate of 10 x 8 cm make gels about 8 x 7 cm with 10, 12, 15 or 17 wells and thickness of 0.75 to 1.5 mm. A casting stand pours several gels at once, and most designs also accept commercial pre-cast cassettes. Runs at 100–200 V take 40–90 minutes. Resolution is adequate for separating proteins from about 5 to 250 kDa, and complex samples may need longer gels.
How does it work?
In a vertical system a polyacrylamide gel is cast between two glass plates separated by spacers and mounted so that its top edge dips into an upper buffer chamber and its bottom edge into a lower one. Voltage across the two chambers drives charged molecules down through the gel. Polyacrylamide forms a tighter and more uniform mesh than agarose, and its pore size is set by total acrylamide percentage and crosslinker ratio, so proteins or fragments differing by a few kilodaltons or a single nucleotide can be resolved. In discontinuous SDS-PAGE, a stacking gel concentrates samples into a sharp band before they enter the resolving gel. Key parts include the plates, spacers, combs, clamps, gaskets, buffer chambers and a cooling core or plate that removes Joule heat.
What are the key features?
- Central core holds one or two gels and forms the upper buffer chamber with low buffer use
- Accepts gels of 0.75, 1.0 and 1.5 mm thickness with 10 to 17 wells
- Casting stand pours up to ten gels at once with consistent gel height
- Compatible with common commercial pre-cast mini gel cassettes of matching size
- Interlocked lid with color-coded leads prevents reversed connection and accidental contact
- Borosilicate glass plates and silicone gaskets provide leak-free sealing over repeated use
What are the technical specifications?
A typical mini vertical gel electrophoresis system for proteins configuration offers gel size (W x L) of approx. 8 x 7 cm, gel thickness options of 0.75, 1.0, 1.5 mm, number of gels per run of 1–4, wells per comb of 10, 12, 15, 17, buffer volume of approx. 600–1000 mL total and maximum voltage of 300 V DC. 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 Mini Vertical Gel Electrophoresis System for Proteins is used in routine SDS-PAGE, protein purity checks, western blot sample preparation and teaching laboratories. Across the wider Vertical Electrophoresis class, laboratories also deploy it for SDS-PAGE protein separation, native PAGE and activity gels and two-dimensional electrophoresis.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61326-1, Ph. Eur. 2.2.31, USP <1053> and ISO 17025. 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.
Assemble plates on a clean, flat surface and check gaskets and spacers for damage before each cast, since leaks ruin gels and contaminate the lower chamber. Acrylamide monomer is neurotoxic, so use gloves and cured gels or pre-cast products where possible. Use fresh APS and TEMED for reproducible polymerisation. Keep buffer chambers filled to the marked level and fit the cooling core for long runs. Clean glass plates with non-abrasive detergent and never use razor blades for separation. Electrical safety follows IEC 61010-1, with interlocked lids and insulated leads. Keep records of gel percentage, buffer batch and run conditions, and verify performance with molecular weight markers.
How do I select the right Mini Vertical Gel Electrophoresis System for Proteins?
Select the mini format for frequent, fast protein checks where sample complexity is moderate. Larger formats resolve complex samples better. In an RFQ specify gel size and thickness, number of gels per run, compatibility with pre-cast cassettes, casting stand capacity, maximum voltage and whether a cooling core is included.
How does it compare with other Vertical Electrophoresis variants?
Decide the gel format from the application. Mini gels of about 8 x 7 cm are quick and economical for routine protein checks and western blot preparation. Midi and large-format gels give longer separation paths for complex samples, and 20 x 20 cm plates are standard for two-dimensional electrophoresis. Sequencing apparatus with long thin plates suits nucleic acid work at single-base resolution. Consider throughput, whether multiple gels must be run and cast together, and whether cooling is needed for long high-voltage runs. Check gel thickness options from 0.75 to 1.5 mm, comb well counts, compatibility with pre-cast gels, and plate and spacer quality, because chipped glass causes leaks. Match the power supply to voltage and current needs, especially for multi-gel runs.
Full specifications
| Gel size (W x L) | approx. 8 x 7 cm |
|---|---|
| Gel thickness options | 0.75, 1.0, 1.5 mm |
| Number of gels per run | 1–4 |
| Wells per comb | 10, 12, 15, 17 |
| Buffer volume | approx. 600–1000 mL total |
| Maximum voltage | 300 V DC |
| Maximum current | 400 mA (two gels) |
| Typical run time | 40–90 min at 100–200 V |
| Protein separation range | approx. 5–250 kDa |
| Plate material | Borosilicate glass |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Routine SDS-PAGE
- Protein purity checks
- Western blot sample preparation
- Teaching laboratories
Key features
- Central core holds one or two gels and forms the upper buffer chamber with low buffer use
- Accepts gels of 0.75, 1.0 and 1.5 mm thickness with 10 to 17 wells
- Casting stand pours up to ten gels at once with consistent gel height
- Compatible with common commercial pre-cast mini gel cassettes of matching size
- Interlocked lid with color-coded leads prevents reversed connection and accidental contact
- Borosilicate glass plates and silicone gaskets provide leak-free sealing over repeated use
Frequently asked questions about Mini Vertical Gel Electrophoresis System for Proteins
Most mini tanks run one or two gels on a single core and up to four gels when a second core or a dummy plate is used. Running more gels raises current, so confirm the power supply can deliver about 200 mA per gel.
Use 12% acrylamide for general work across 15–100 kDa, 8% for proteins above 100 kDa and 15% for proteins below 30 kDa. Gradient gels of 4–20% cover a wide range in one run.
A standard mini gel runs about 40–90 minutes at 100–200 V, stopping when the bromophenol blue dye front reaches the bottom of the gel. Constant voltage at the lower end gives sharper bands and less heating.
A vertical system runs polyacrylamide gels between glass plates to separate proteins and short nucleic acids with high resolution. It is used for SDS-PAGE, native PAGE, two-dimensional electrophoresis, sequencing gels and preparing samples for western blotting.
Polyacrylamide forms a finer and more uniform mesh whose pore size is tuned by acrylamide percentage and crosslinker. This resolves proteins and small nucleic acids that differ by a few kilodaltons or a single base, which agarose cannot separate.
Leaks usually come from chipped glass plates, worn gaskets, misaligned spacers or over-tightened clamps. Inspect the plate edges, replace damaged gaskets, assemble on a flat surface and test with water before pouring the gel.
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