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Nitroglycerin ALDH2 gene polymorphism detection method and device

A gene polymorphism and detection device technology, which is applied in the field of medical detection, can solve the problems of affecting detection results and reagent bottles are easily broken

Inactive Publication Date: 2021-07-30
南京美之联医学检验实验室有限公司
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  • Claims
  • Application Information

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Problems solved by technology

[0004] The purpose of the present invention is to provide a method and device for detecting polymorphism of nitroglycerin ALDH2 gene, aiming to solve the technical problem that the reagent bottle is easily broken during the detection process of the detection personnel in the prior art, which affects the detection result

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  • Nitroglycerin ALDH2 gene polymorphism detection method and device
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  • Nitroglycerin ALDH2 gene polymorphism detection method and device

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Embodiment Construction

[0031] Embodiments of the present invention are described in detail below, examples of which are shown in the drawings, wherein the same or similar reference numerals designate the same or similar elements or elements having the same or similar functions throughout. The embodiments described below by referring to the figures are exemplary and are intended to explain the present invention and should not be construed as limiting the present invention.

[0032] In describing the present invention, it should be understood that the terms "length", "width", "upper", "lower", "front", "rear", "left", "right", "vertical", The orientation or positional relationship indicated by "horizontal", "top", "bottom", "inner", "outer", etc. are based on the orientation or positional relationship shown in the drawings, and are only for the convenience of describing the present invention and simplifying the description, rather than Nothing indicating or implying that a referenced device or element...

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Abstract

The invention relates to the technical field of medical detection, and concretely relates to a nitroglycerin ALDH2 gene polymorphism detection method and device. A detector is fixedly connected with an operation table and located above the operation table, a containing groove is formed in the operation table, a storage box is detachably connected with the operation table and located in the containing groove, a supporting rod is detachably connected with the storage box and located in the storage groove, an embedding ring is fixedly connected with the supporting rod and penetrates through the supporting rod, and a first rotating shaft is fixedly connected with one end of the supporting rod. A second rotating shaft is fixedly connected with the other end of the supporting rod, the two ends of a holding rod are rotationally connected with the first rotating shaft and the second rotating shaft respectively, and each stabbing rod is fixedly connected with the supporting rod. Reagent bottles are driven to leave the storage box when the stabbing rods are embedded with the reagent bottles and the holding rod is lifted, so that the reagent bottles are prevented from being broken and affecting the detection result in the detection process of detection personnel .

Description

technical field [0001] The invention relates to the technical field of medical detection, in particular to a method and device for detecting polymorphism of nitroglycerin ALDH2 gene. Background technique [0002] The ALDH2 gene is the gene encoding mitochondrial acetaldehyde dehydrogenase, which has dehydrogenase activity and plays a major role in the oxidation of acetaldehyde in the human body; precision medicine is an important part of precision medicine, pharmacogenetics and pharmacogenomics research has been It has been confirmed that different patients carry different gene single nucleotide polymorphisms and respond differently to drugs, and the curative effect of the same drug on different patients is also very different. Genetic testing to guide precise medication can help doctors screen out effective treatments plan to make the most correct treatment decision for the patient. [0003] At present, the detection method of gene polymorphism is the fluorescent quantitat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12M1/34C12M1/24C12M1/00
CPCC12Q1/6858C12Q2531/113C12Q2563/107
Inventor 范永敢
Owner 南京美之联医学检验实验室有限公司
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