Gene detecting device integrating extraction, amplification and detection
A gene detection and cylinder technology, which is applied in the general fields of molecular biology and medicine, can solve the problems of inability to directly observe the detection results, inconvenient to carry instruments, cumbersome steps, etc., so as to achieve no need for special equipment, and the operation is simple and easy to carry out. , the effect of simple operation
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Embodiment 1
[0083] Example 1: Sample flow through a preferred portable device
[0084] The portable device has two medium and long cylinders, the first hollow long cylinder (1) is used for extracting and amplifying the target nucleic acid sequence, and the second hollow long cylinder (25) is used for detecting the nucleic acid sequence. The sample is added to the first compartment (12) located in the cylinder (1), the compartment (12) contains a dry lysis reagent for nucleic acid extraction, and the sample provides a liquid for resuspending the lysis reagent. Tighten the screw cap (2), after incubating for a period of time, remove the fixing ring (10) on the upper end of the screw cap (2), and slowly push the push rod (6) to the scale A, that is, there is a second fixing ring (11). ) position, at this time, the liquid flows into the filter system (14), after two minutes, remove the fixed ring (11), and push the push rod (6) to the bottom, at this time, the filtered nucleic acid flows into...
Embodiment 2
[0085] Example 2: Sample Extraction System
[0086] A non-limiting example of an extraction system can include:
[0087] Lysates used to concentrate buffer components of DNA or RNA samples, and may include specially treated multi-layer absorbents, as well as extraction solutions including but not limited to detergents and alkaline buffers.
[0088]This lysate disrupts cell walls or membranes and exposes genetic samples such as DNA or RNA to the solution. It is envisaged that proteases may be added to remove proteins and cell walls. Alternatively, separate solution-type coatings or multilayer films may be used.
[0089] In addition, various reservoirs, activated carbon filters, and ion exchange filters can be used. In addition, the filter can be a semipermeable membrane with a molecular cut-off ranging from 60,000 to 300,000 D or higher and can be non-stick coated.
[0090] The filtration system removes all potential inhibitors, small molecules, ions, and proteins.
[0091...
Embodiment 3
[0092] Example 3: Nucleic Acid Amplification
[0093] Nucleic acid isothermal amplification technology is characterized in that the whole process of the amplification reaction (except the initial hybridization step) is carried out at a single temperature, and does not need to be carried out under a special amplification instrument, unlike the PCR reaction, which needs to undergo dozens of temperature changes cycle process. This feature of the isothermal amplification technology enables it to support the isothermal amplification platform used in the portable device of the present invention, and the temperature required for the amplification is achieved by a heating loop.
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