CN103308587A - Hollow fiber electrophoresis gel imaging system - Google Patents
Hollow fiber electrophoresis gel imaging system Download PDFInfo
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- CN103308587A CN103308587A CN2013102080595A CN201310208059A CN103308587A CN 103308587 A CN103308587 A CN 103308587A CN 2013102080595 A CN2013102080595 A CN 2013102080595A CN 201310208059 A CN201310208059 A CN 201310208059A CN 103308587 A CN103308587 A CN 103308587A
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Abstract
本发明涉及一种空芯光纤电泳凝胶成像系统,包括能够调焦的CCD或CMOS摄像头,步进电动机,高压电源电极,第一滤光片,空芯光纤,触摸屏LED显示器,第二滤光片,紫外灯和成像暗箱;所述两个高压电源电极中间布置有一根或多根空芯光纤,所述摄像头安装在空芯光纤的上方,通过步进电动机驱动左右水平移动,摄像头的底部安装有第一滤光片;所述第二滤光片布置在空芯光纤的下方,第二滤光片下方为紫外灯;所述触摸屏LED显示器用来控制成像系统;空芯光纤中为凝胶,待测生物或药物分子样品滴加在空芯光纤的一端,利用空芯光纤作为电泳的泳道和光束传导的通道,对样品进行电泳凝胶成像及分子光谱分析检测。本系统具有样品用量少,灵敏高效,无污染等特点。
The invention relates to a hollow-core optical fiber electrophoresis gel imaging system, which includes a CCD or CMOS camera capable of focusing, a stepping motor, a high-voltage power supply electrode, a first optical filter, a hollow-core optical fiber, a touch screen LED display, and a second optical filter film, ultraviolet lamp and imaging obscura; one or more hollow-core optical fibers are arranged between the two high-voltage power supply electrodes, and the camera is installed above the hollow-core optical fiber, driven by a stepping motor to move left and right horizontally, and the bottom of the camera is installed There is a first optical filter; the second optical filter is arranged under the hollow-core optical fiber, and the ultraviolet lamp is below the second optical filter; the touch-screen LED display is used to control the imaging system; the hollow-core optical fiber is a gel The biological or drug molecule sample to be tested is dropped on one end of the hollow-core optical fiber, and the hollow-core optical fiber is used as the electrophoresis swimming lane and the beam conduction channel to perform electrophoresis gel imaging and molecular spectral analysis and detection on the sample. The system has the characteristics of less sample consumption, high sensitivity and high efficiency, and no pollution.
Description
技术领域 technical field
本发明涉及一种空芯光纤电泳凝胶成像系统。 The present invention relates to a hollow-core optical fiber electrophoresis gel imaging system.
背景技术 Background technique
核酸凝胶电泳是分子生物学实验中分离、鉴定和纯化核酸分子、探针、扩增产物的一种常用方法。它的基本原理是将凝胶置电场中,利用中性pH值下带电荷的核酸通过凝胶网孔向阳极迁移的特性,电泳适当时间后大小、构象不同的核酸片段将呈梯状排列在凝胶不同位置上,从而达到分离的目的。核酸的迁移速率受到分子大小、构象、琼脂糖浓度、施加电压、电场、电泳缓冲液、嵌入染料量等多因素影响。 正因如此,传统的核酸电泳成像效果受多种实验条件和参数的影响,难以实现重复性和精确性的有机统一。同时,核酸电泳的常用染料溴化乙锭(ethidium bromide,EB)是一种强的诱变剂并有中度毒性,使用操作上的不规范容易给人体健康和环境带来不利的影响。 Nucleic acid gel electrophoresis is a common method for separating, identifying and purifying nucleic acid molecules, probes and amplification products in molecular biology experiments. Its basic principle is to place the gel in an electric field, and use the characteristic of the charged nucleic acid at neutral pH to migrate to the anode through the gel mesh. After electrophoresis for an appropriate time, the nucleic acid fragments with different sizes and conformations will be arranged in a ladder shape. Gel in different positions, so as to achieve the purpose of separation. The migration rate of nucleic acid is affected by many factors such as molecular size, conformation, agarose concentration, applied voltage, electric field, electrophoresis buffer, and the amount of intercalating dye. Because of this, the effect of traditional nucleic acid electrophoresis imaging is affected by various experimental conditions and parameters, and it is difficult to achieve the organic unity of repeatability and accuracy. At the same time, ethidium bromide (EB), a commonly used dye for nucleic acid electrophoresis, is a strong mutagen and moderately toxic, and irregular use and operation may have adverse effects on human health and the environment.
发明内容 Contents of the invention
针对现有技术存在的缺陷,本发明的目的是提供一种空芯光纤电泳凝胶成像系统,集光学分析检测与电泳与一体化,实现一体化检测。本系统是集核酸电泳、光学成像、数据采集与分析,检测生物核酸分子的“一站式”实验研究平台,用来测定生物医学分子的电学、光学、及凝胶图像、对分子多方位检测。 In view of the defects existing in the prior art, the purpose of the present invention is to provide a hollow-core optical fiber electrophoresis gel imaging system, which integrates optical analysis detection and electrophoresis, and realizes integrated detection. This system is a "one-stop" experimental research platform integrating nucleic acid electrophoresis, optical imaging, data acquisition and analysis, and detection of biological nucleic acid molecules. It is used to determine the electrical, optical, and gel images of biomedical molecules, and to detect molecules in multiple directions. .
为达到上述目的,本发明采用如下技术方案: To achieve the above object, the present invention adopts the following technical solutions:
一种空芯光纤电泳凝胶成像系统,包括能够调焦的CCD或CMOS摄像头,步进电动机,高压电源电极,第一滤光片,空芯光纤,触摸屏LED显示器,第二滤光片,紫外灯和成像暗箱;所述两个高压电源电极中间布置有一根或多根空芯光纤,所述摄像头安装在空芯光纤的上方,通过步进电动机驱动左右水平移动,摄像头的底部安装有第一滤光片;所述第二滤光片布置在空芯光纤的下方,第二滤光片下方为紫外灯;所述摄像头,步进电动机,高压电源电极,第一滤光片,空芯光纤,第二滤光片和紫外灯置于所述成像暗箱中,所述触摸屏LED显示器安装在成像暗箱外侧,用来控制成像系统;空芯光纤中为凝胶,待测生物或药物分子样品滴加在空芯光纤的一端,利用空芯光纤作为电泳的泳道和光束传导的通道,对样品进行电泳凝胶成像及分子光谱分析检测。 A hollow-core optical fiber electrophoresis gel imaging system, including a CCD or CMOS camera capable of focusing, a stepping motor, a high-voltage power supply electrode, a first optical filter, a hollow-core optical fiber, a touch-screen LED display, a second optical filter, and an ultraviolet Lamp and imaging obscura; one or more hollow-core optical fibers are arranged between the two high-voltage power supply electrodes, the camera is installed above the hollow-core optical fiber, and is driven by a stepping motor to move left and right horizontally, and the bottom of the camera is installed with a first Optical filter; the second optical filter is arranged below the hollow-core optical fiber, and the ultraviolet lamp is below the second optical filter; the camera, stepping motor, high-voltage power supply electrode, the first optical filter, and hollow-core optical fiber , the second optical filter and the ultraviolet lamp are placed in the imaging dark box, and the touch screen LED display is installed outside the imaging dark box to control the imaging system; the hollow-core optical fiber is a gel, and the biological or drug molecule sample drops It is added to one end of the hollow-core fiber, and the hollow-core fiber is used as the electrophoresis swimming lane and the beam conduction channel to perform electrophoresis gel imaging and molecular spectrum analysis and detection on the sample.
与现有技术相比,本发明具有如下突出的实质性特点和显著地优点: Compared with the prior art, the present invention has the following prominent substantive features and significant advantages:
本发明空芯光纤电泳凝胶成像系统可以从光学成像,分子光谱分析,电泳电场分离等多个层次同时检测分子。该系统的主要原理仍是通过带电核酸分子在电泳缓冲液分级分离,所不同的是核酸电泳的载体是空心光纤,该光纤一方面能够传导光束,传导光束经过分子后承载分子的信息可以进行探测分析,另一方面能否在其空心中作为电泳的泳道对分子进行电场作用等的分离,可以有效克服核酸分子在电泳过程中受管壁上解离因的素影响,如表面电荷、表面活性剂、蛋白质等。染料分子EB直接灌注于光纤管中,避免了与外界的接触,可有效减少污染。输出信号由光信号采集系统,将紫外照射嵌入核酸分子染料EB所得的荧光强度转换为数字信号,可降低传统核酸凝胶电泳中常见的背景干扰。综上所述,该系统具有样品用量少,灵敏高效,无污染等特点。 The hollow-core optical fiber electrophoresis gel imaging system of the present invention can simultaneously detect molecules from multiple levels such as optical imaging, molecular spectrum analysis, and electrophoresis electric field separation. The main principle of this system is still the separation of charged nucleic acid molecules in the electrophoresis buffer. The difference is that the carrier of nucleic acid electrophoresis is a hollow fiber. On the one hand, the fiber can conduct light beams, and the information carried by the light beams after passing through the molecules can be detected. On the other hand, whether it can be used as an electrophoresis lane in the hollow to separate molecules by electric field action can effectively overcome the influence of nucleic acid molecules on the tube wall during electrophoresis, such as surface charge and surface activity. agents, proteins, etc. The dye molecule EB is directly poured into the fiber tube, avoiding contact with the outside world, which can effectively reduce pollution. The output signal is converted into a digital signal by the optical signal acquisition system, which converts the fluorescence intensity obtained by ultraviolet irradiation of embedded nucleic acid molecule dye EB, which can reduce the common background interference in traditional nucleic acid gel electrophoresis. In summary, the system has the characteristics of less sample consumption, high sensitivity and high efficiency, and no pollution.
附图说明 Description of drawings
图1是本发明涉及的新型凝胶成像系统的总体设计示意图。 Figure 1 is a schematic diagram of the overall design of the novel gel imaging system involved in the present invention.
具体实施方式 Detailed ways
本发明的优选实施例结合附图详述如下: Preferred embodiments of the present invention are described in detail as follows in conjunction with accompanying drawings:
参见图1,一种空芯光纤电泳凝胶成像系统,包括能够调焦的CCD或CMOS摄像头1,步进电动机2,高压电源电极3,第一滤光片4,空芯光纤5,触摸屏LED显示器6,第二滤光片7,紫外灯8和成像暗箱9;所述两个高压电源电极3中间布置有一根或多根空芯光纤5,所述摄像头1安装在空芯光纤5的上方,通过步进电动机2驱动左右水平移动,摄像头1的底部安装有第一滤光片4;所述第二滤光片7布置在空芯光纤5的下方,第二滤光片7下方为紫外灯8;所述摄像头1,步进电动机2,高压电源电极3,第一滤光片4,空芯光纤5,第二滤光片7和紫外灯8置于所述成像暗箱9中,所述触摸屏LED显示器6安装在成像暗箱9外侧,用来控制成像系统;空芯光纤5中为凝胶,待测生物或药物分子样品滴加在空芯光纤5的一端,利用空芯光纤5作为电泳的泳道和光束传导的通道,对样品进行电泳凝胶成像及分子光谱分析检测。
Referring to Fig. 1, a hollow-core optical fiber electrophoretic gel imaging system includes a focusable CCD or CMOS camera 1, a
本实施例中摄像头1采用日本索尼公司APR-2110Z可调焦CCD摄像头;采用直径为420μm的空芯光纤5,共20根;高压电源电压为1kv;采用的凝胶为琼脂糖凝胶;被测试样品为DNA marker即DNA分子量标准物和噬菌体展示库中的一个噬菌体的PCR片段。样品添加并电泳上电后,采集到清晰的凝胶成像图片。
In the present embodiment, the camera 1 adopts the APR-2110Z adjustable focus CCD camera of Sony Corporation of Japan; adopting a diameter of 420 μm hollow-core
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107860813A (en) * | 2017-11-16 | 2018-03-30 | 上海仪龙生物科技有限公司 | A kind of PhastGel electrophoresis and real-time imaging devices |
CN111812091A (en) * | 2020-06-28 | 2020-10-23 | 上海交通大学 | Chip gel electrophoresis and its online UV-VIS imaging detection device |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5324401A (en) * | 1993-02-05 | 1994-06-28 | Iowa State University Research Foundation, Inc. | Multiplexed fluorescence detector system for capillary electrophoresis |
JPH09281078A (en) * | 1996-04-09 | 1997-10-31 | Hitachi Electron Eng Co Ltd | Dna base sequence determining apparatus |
US20010054554A1 (en) * | 2000-04-13 | 2001-12-27 | Janusz Pawliszyn | Measurement of fluorescence using capillary isoelectric focusing |
CN1865932A (en) * | 2005-05-19 | 2006-11-22 | 清华大学 | Fluorometric detector for micro-fluidic chip system |
CN1869662A (en) * | 2006-05-15 | 2006-11-29 | 清华大学 | Multi-channel column imaging fluorescent detector |
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Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5324401A (en) * | 1993-02-05 | 1994-06-28 | Iowa State University Research Foundation, Inc. | Multiplexed fluorescence detector system for capillary electrophoresis |
JPH09281078A (en) * | 1996-04-09 | 1997-10-31 | Hitachi Electron Eng Co Ltd | Dna base sequence determining apparatus |
US20010054554A1 (en) * | 2000-04-13 | 2001-12-27 | Janusz Pawliszyn | Measurement of fluorescence using capillary isoelectric focusing |
CN1865932A (en) * | 2005-05-19 | 2006-11-22 | 清华大学 | Fluorometric detector for micro-fluidic chip system |
CN1869662A (en) * | 2006-05-15 | 2006-11-29 | 清华大学 | Multi-channel column imaging fluorescent detector |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107860813A (en) * | 2017-11-16 | 2018-03-30 | 上海仪龙生物科技有限公司 | A kind of PhastGel electrophoresis and real-time imaging devices |
CN111812091A (en) * | 2020-06-28 | 2020-10-23 | 上海交通大学 | Chip gel electrophoresis and its online UV-VIS imaging detection device |
CN111812091B (en) * | 2020-06-28 | 2023-09-05 | 上海交通大学 | Chip gel electrophoresis and online UV-VIS imaging detection device thereof |
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