Use dd-Water to eliminate your  Gel Smiling

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Solving-gel-smiling-problem

Get 6mgel to eliminate gel smiling

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        Use dd-Water to eliminate gel smiling                                        

Click "Order Status" to see who are using Biokeystone's smiling-free gel system

 

The main causes of gel smiling problem: 

a. Uneven distribution of electric field across gel width

b. Uneven elevation of temperature among different lanes

As a user, you can do nothing about uneven electric field (your gel system has been permanently manufactured that way). The only thing you can do is to run the gel slowly so that the gel temperature unevenness is less significant.

 

6mgel, Smiling-free high speed gel system in 6 minutes

The innovative feature of straight banding technology:

a. Edge compensation of electrode for even electric field

b. Direct dd-water cooling on gel top for uniform temperature distribution

 

Using 6Mgel, the problem of gel smiling is simply eliminated, as shown below.

  The Breakthrough of high-speed electrophoresis without running buffer

  See User Feedback about the performance of buffer-less high speed electrophoresis:

" The Liberty bufferless gel system is the best gel electrophoresis system we've ever used. It's not only easy to set up, robust, and fast, but generates excellent results without the need of running buffer. Highly recommended. See our genotyping service picture below." ---- Ivan Delgado Orlic, President and CEO, Mouse Genotype Co. 

 

 

 

6Mgel Principle of smiling free technologies

 

1x running buffer, a highly conductive liquid, has two functions in conventional submarine agarose gel electrophoresis: keeping the agarose gel cooled and conducting electric current.

horizontal gel electrophoresis diagram

 

To avoid gel overheating, the volume of running buffer should be as large as possible. But more buffer conducts more electric current, which generates more heat. So buffer volume should be as small as possible. Which is correct - more buffer or less buffer?

 

The principle of the 6Mgel invention

The inventor of 6mgel recognized that water is the best and cheapest coolant. The electrical resistance of lab dd-water is 18MΩ, which means that dd-water is an excellent electrical insulator. By simply adding dd-water directly on top of the buffer-containing agarose gel, the desired effects are achieved: gels can be run much faster!  You can add a large volume of dd-water to dissipate heat so that a much higher voltage can be applied to drive faster migration of DNA molecules. Band "smiling" is eliminated because the large volume of dd-water in direct contact with the gel maintains even heat distribution. Also, sharper banding occurs due to "stacking effects of dd-water in gel wells.

In 6Mgel, the V/cm in wells is elevated about 3-fold higher than in the gel body, which drives DNA 3 times faster in wells than in the gel body, resulting in sharper bands. Furthermore, consumption of running buffer can be reduced by 50-75%.

 

The strength of 6Mgel is particularly significant for Genotyping and PCR applications, where high percentage agarose gels are usually required. It takes longer time for sample molecules to migrate through the concentrated gel body. 6Mgel innovation has solved the problem.

 

During the development of 6Mgel, more and more features were added, such as buffer-less high speed electrophoresis, lab-made precast gels for high-speed electrophoresis, and agarose-saving gel systems. Go to 6mgel systems for more information.

 

The most welcomed products

  Glass Coverslips

Tested for primary cell and neuron cultures, manufactured in Germany

Uncoat German coverslips in box

PLL coated coverslips, sterile

PDL coated coverslips, sterile

Collagen coated coverslips, sterile

Gelatin coated coverslips, sterile

Custom coating coverslips, sterile

Pre-cleaned coverslips, sterile

 

 

Liberty 120 rapid electrophoresis system

Agarose-saving high-speed gel electrophoresis

See Genotyping / PCR results in 6 minutes

One-step genotyping DNA extraction kit

Buffer-less gel electrophoresis instrument

Most recognized gel electrophoresis apparatus

Gel electrophoresis unit comparison

Horizontal gel principle

PCR gel features