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Method for detecting polymorphism of human gastric cancer susceptible genes IL17A rs3748067 by aid of ApoI

A gene polymorphism, susceptibility gene technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of low specificity and poor specificity of dye method, and achieve a wide range of applications and low cost. , the effect of simple operation

Inactive Publication Date: 2016-06-22
ZHENGZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] The disadvantage of the dye method for qualitative gene analysis is that the specificity of the dye method is not strong, as long as it is a double-stranded DNA, it will bind and emit light, so the specificity is poor

Method used

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  • Method for detecting polymorphism of human gastric cancer susceptible genes IL17A rs3748067 by aid of ApoI
  • Method for detecting polymorphism of human gastric cancer susceptible genes IL17A rs3748067 by aid of ApoI
  • Method for detecting polymorphism of human gastric cancer susceptible genes IL17A rs3748067 by aid of ApoI

Examples

Experimental program
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Embodiment 1

[0071] Example 1. Determination of Human IL17Ars3748067 Polymorphism in Human Gastric Cancer Tissue Specimens

[0072] In a specific embodiment of the present invention, the specific steps for detecting human IL17A gene polymorphism rs3748067 are as follows:

[0073] (1) Obtain the surgically excised gastric cancer tissue, and use the phenol-chloroform method to extract the genomic DNA of the gastric cancer tissue as the DNA to be tested. The extraction steps are as follows:

[0074] 1) Thaw the gastric cancer tissue block, wash away blood stains with normal saline, cut out 0.1g of tissue for grinding, add 1ml of sterilized water, mix upside down, centrifuge at 10000rpm for 10min, discard the supernatant, repeat the above steps twice

[0075] 2) Add 200 μl of DNA lysate and 5 μl of proteinase K, mix well, and digest overnight in a water bath at 55°C.

[0076] 3) After the digestion is completed, add an equal volume of phenol-chloroform mixture (1:1) and shake vigorously to ma...

Embodiment 2

[0086] Example 2. Determination of human IL17Ars3748067 polymorphism in human peripheral blood whole blood samples

[0087] The steps are basically the same as in Example 1, except that the following method is used to extract genomic DNA from human peripheral blood as the DNA to be tested.

[0088] Follow the operation steps of NEP004-1 Whole Blood Genomic DNA Extraction Kit to extract the genomic DNA of the blood sample to be tested. The specific steps are as follows:

[0089] 1) After adding 300 μl of blood cells into a 1.5ml centrifuge tube, add 900 μl of cell lysate and mix evenly. After placing it on ice for 10 minutes, centrifuge at 12,000 rpm for 1 minute in a centrifuge, discard the supernatant, add 900 μl of cell lysate again, and use a gun to After blowing up the precipitate and mixing it, repeat the above steps;

[0090] 2) Add 600 μl solution B solution to the precipitate, gently blow up the precipitate with a pipette gun, add 10 μl proteinase K and mix well, plac...

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Abstract

The invention discloses a method for detecting the polymorphism of human gastric cancer susceptible genes IL17A rs3748067 by the aid of ApoI. The method includes amplifying target DNA (deoxyribonucleic acid) fragments by means of polymerase chain reaction; digesting to-be-detected DNA fragments by the aid of restriction incision enzymes; identifying and cutting specific sequences by the aid of the restriction incision enzymes; carrying out electrophoresis on digested products; analyzing cleavage sites of the sequences of the fragments by the aid of restriction maps; comparing the difference of gene sequences from different sources by the aid of the diversity of the fragments. The method has the advantages that briefly speaking, the corresponding target fragments are amplified by means of PCR (polymerase chain reaction) at first, then digestion reaction is carried out by the aid of the restriction incision enzymes, the restriction maps are observed and compared after electrophoresis is carried out, and accordingly the difference between the sequences can be analyzed; the method is good in repeatability, easy to implement and low in cost, and digestion results are easy to identify; the method and detection reagent kits which are easy to implement, low in cost and wide in application range can be provided for detecting the polymorphism of the human gastric cancer susceptible genes IL17A rs3748067.

Description

technical field [0001] The invention belongs to the field of biotechnology, and relates to a method for detecting polymorphism of human gastric cancer susceptibility gene IL17Ars3748067 by using ApoI. Background technique [0002] Single nucleotide polymorphism (singlenucleotide polymorphism, SNP) mainly refers to the DNA sequence polymorphism caused by the variation of a single nucleotide at the genome level. It is the most common type of heritable variation in humans. Accounts for more than 90% of all known polymorphisms. SNPs exist widely in the human genome, with an average of 1 in every 500-1000 base pairs, and it is estimated that the total number can reach 3 million or more. CAPs (cleaved amplification polymorphism sequence-tagged sites) CAPs technology is also called PCR-RFLP, restriction fragment length polymorphism polymerase chain reaction (PCR-RFLP) technology. The basic principle of PCR-RFLP is to use PCR to amplify the target DNA, and then the amplified prod...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68
CPCC12Q1/6858C12Q2521/301C12Q2565/125
Inventor 王凯娟高三友侯瑞生李丽徐娅娟和红杨倩董凯艳段富交胡艳丽
Owner ZHENGZHOU UNIV
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