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A kind of Coomassie brilliant blue dyeing solution and dyeing method

A Coomassie Brilliant Blue and staining solution technology, which is applied in the field of Coomassie Brilliant Blue staining solution, can solve the problems of lengthy cycle and many dyeing steps, and achieve the effects of small background interference, saving dyeing time and simplifying operation steps

Active Publication Date: 2016-01-20
BEIJING VICNOVO SCI TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] The present invention solves the problems in the prior art that when staining protein bands in protein gels, the Coomassie Brilliant Blue staining solution used contains reagents harmful to the human body, and the staining steps are numerous and the cycle is lengthy, and further provides An improved Coomassie Brilliant Blue dyeing solution and a dyeing method. The dyeing solution does not contain harmful reagents to the human body and is environmentally friendly. The dyeing method using the dyeing solution can complete the entire dyeing process within 20 minutes, and after dyeing Does not require decolorization treatment, has the advantages of short cycle time, high sensitivity, and low background interference

Method used

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  • A kind of Coomassie brilliant blue dyeing solution and dyeing method
  • A kind of Coomassie brilliant blue dyeing solution and dyeing method
  • A kind of Coomassie brilliant blue dyeing solution and dyeing method

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Embodiment 1

[0041]The Coomassie Brilliant Blue staining solution described in this embodiment is 5% phosphoric acid by volume, 8% ethanol by volume, soluble starch with a mass volume concentration of 10g / L, and a mass volume concentration of 100mg / L Coomassie Brilliant Blue G250, the balance is water. The specific preparation steps are as follows: Take 50 parts by weight of Coomassie Brilliant Blue G250 and dissolve it in 200 parts by volume of deionized water, slowly add 25 parts by volume of phosphoric acid, stir well, add 40 parts by volume of ethanol, stir again and add high pressure 100 parts by volume of an aqueous solution containing 5,000 parts by weight of soluble starch after bacteria was stirred evenly, and then the volume was fixed to 500 parts by volume with deionized water.

[0042] Wherein, the preparation method of the soluble starch described in this embodiment is as follows: (1) adding hydrochloric acid with a mass concentration of 3% to the millet starch to make a solu...

Embodiment 2

[0047] The Coomassie Brilliant Blue staining solution described in this embodiment is 8% sulfuric acid by volume, 10% ethanol by volume, soluble starch with a mass volume concentration of 20g / L, and a mass volume concentration of 50mg / L Coomassie Brilliant Blue R250 aqueous solution. Its specific preparation steps are as follows: Take 25 parts by weight of Coomassie Brilliant Blue R250 and dissolve it in 200 parts by volume of deionized water, slowly add 40 parts by volume of sulfuric acid, stir well, add 50 parts by volume of ethanol, stir again and add high pressure 100 parts by volume of an aqueous solution containing 10,000 parts by weight of soluble starch after bacteria was stirred evenly, and the volume was adjusted to 500 parts by volume with deionized water.

[0048] Wherein the preparation method of the soluble starch is as follows: (1) adding hydrochloric acid with a mass concentration of 6% to the millet starch to make a solution, stirring the solution into a thin...

Embodiment 3

[0053] The Coomassie Brilliant Blue staining solution described in this embodiment is 0.5% sulfuric acid by volume, 5% ethanol by volume, soluble starch with a mass volume concentration of 50g / L, and a mass volume concentration of 500mg / L Coomassie Brilliant Blue R250 aqueous solution. Its specific preparation steps are as follows: take 250 parts by weight of Coomassie Brilliant Blue R250 and dissolve it in 200 parts by volume of deionized water, slowly add 2.5 parts by volume of sulfuric acid, stir well, add 25 parts by volume of ethanol, stir again and add high pressure 100 parts by volume of an aqueous solution containing 25,000 parts by weight of soluble starch after bacteria was stirred evenly, and then adjusted to 500 parts by volume with deionized water.

[0054] Wherein the preparation method of the soluble starch is as follows: (1) adding hydrochloric acid with a mass concentration of 3% to cornstarch to make a solution, stirring the solution into a thin paste, soaki...

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Abstract

The invention discloses a coomassie brilliant blue staining solution and a staining method. The coomassie brilliant blue staining solution comprises 0.1-10 percent by volume of acid, 1-15 percent by volume of ethyl alcohol, 10-50g / L of soluble starch and 20-1000mg / L of coomassie brilliant blue aqueous solution. The staining solution does not contain reagents harmful to human bodies and is environmental friendly. The staining method using the staining solution has the beneficial effects that due to addition of the soluble starch, the staining background of gel can be reduced, a protein band can be specifically stained, the sensitivity of staining is effectively improved, and therefore, the whole staining process of the protein band can be completed within 20 minutes by using the staining method, the steps such as gel fixation, sensitization and destaining in a conventional dyeing process are omitted, operating steps are greatly simplified, and the dyeing time is saved; the staining method has the advantages of short cycle, high sensitivity and small background interference.

Description

technical field [0001] The invention relates to a Coomassie brilliant blue staining solution and a dyeing method using the staining solution, belonging to the field of biotechnology. technical background [0002] In the 1960s, there were reports of staining protein bands after electrophoresis with Coomassie brilliant blue staining solution to observe protein components and protein separation. In the following decades, Coomassie brilliant blue staining has become one of the standard methods for observing protein bands in protein gel electrophoresis in protein science research. This staining method is included in almost all protein research manuals. Both are described. In the classic method of staining protein gels with Coomassie Brilliant Blue, Coomassie Brilliant Blue is usually dissolved in a solvent containing acetic acid, methanol, etc. The steps of staining and decolorization take 1-2 days. It can be seen that the staining process of protein gels not only has many step...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C09B67/10G01N1/30
Inventor 高建恩王清明罗时伟钱军
Owner BEIJING VICNOVO SCI TECH
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