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Until far back, however, the studies of biology generally showed the difficulty of obtaining the most precise results, as only a weak band of the DNA electrophoresis signal occurs near the 0.1 m mark. As a result, the use of the DNA electrophoresis device has had its critics such that most of the studies were unsuccessful because the sample was likely of a highly contaminating non-specific band at this step. However, the poor binding as found by the method was widely identified as the one that caught the most attention. Also, more sophisticated problems such as the low sensitivity of the electrophoresis device simply could not be solved by applying similar techniques for subsequent experiments. Consequently, a great deal of attention was put on the development of a similar gene expression array, however all the techniques available on this technology at the time looked something like those mentioned above. (1) Method 1 First, we wanted to understand how this method works. When one wants to obtain a sample by simply comparing the DNA signal to a sample, the DNA electrophoresis device just computes a sequence of nucleotides and uses the DNA electrophoresis signal to provide the molecular weight of the detected gel. The most accurate method for this purpose is to use a digital dye. (2) Method 2 Next, we wanted to see how this method can be used for gene expression. For instance, suppose we wanted to study how the expression level, assessed by microarray, changes with the redox-neutrality of the cell. Method 1 A paper in Nature Communications check here a comparison between many of the methods in the field of gene expression and the DNA electrophoresis technology. The paper describes the DNA electrophoresis device (see section S1) with the following parameters: the volume of cells to be analyzed is approximately 5 µL (an experiment setting two cells). Suppose the sample is allowed to stay under-oxidize for a short time in a double strand DNA structure (the redox process) 1 µL/ml of DNA solution. The total cells amount also is approximately 10^6^ cells for the first time. The total DNA electrophoretisation rate may be decreased by increasing the volume of cells which are not allowed to become oxidized. See [2]. Two cells of the DNA electrophoresis device are each called Lox and Rox or Lyra. The Lox is formed by phosphorylation of 4-