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Human papilloma virus (24 types) detection (fluorescent PCR method) kit and detection method

A detection method and technique for papilloma, which are applied in the directions of fluorescence/phosphorescence, biochemical equipment and methods, and determination/inspection of microorganisms, to achieve the effect of avoiding the decline of amplification efficiency

Inactive Publication Date: 2014-04-16
JIANGSU MOLE BIOSCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0019] The above patents and products can only detect up to 14 HPV types in one tube, and the cost increase caused by the use of new probes makes it difficult to apply to clinical diagnosis

Method used

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  • Human papilloma virus (24 types) detection (fluorescent PCR method) kit and detection method
  • Human papilloma virus (24 types) detection (fluorescent PCR method) kit and detection method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Example 1: Primer probe design

[0056] Studies have shown that the L1 regions of various types of HPV genomes have both certain homology and certain specificity, and degenerate primers can be designed according to the homologous sequences. The present invention detects the primer probe design principle of 24 types of HPV DNA is: the L1 region of HPV genome of each type selects the sequence with high homology to design forward and reverse primers, and designs the probe sequence at the sequence with high specificity, Perform PCR in the same tube while using Taqman probes to detect 24 types of HPV. The template denaturation temperature is 95°C; the primer annealing and extension temperature is 52°C; the number of cycles for the amplification reaction is 35-45.

[0057] Table 1 is the gene bank number of the amplified target sequence

[0058] HPV type Genebank number target sequence position HPV6 probe X00203 6227-6409 HPV11 probe M14119 6220-...

Embodiment 2

[0059] Example 2: Sample Preparation

[0060] In order to quickly and easily prepare HPV DNA templates that can be used for PCR amplification, the present invention uses a non-ionic detergent in conjunction with a high temperature environment to crack the HPV outer membrane protein to release the DNA therein, and uses chelex-100 to remove the metal therein Impurities such as ions that inhibit PCR can be used to improve detection efficiency.

Embodiment 3

[0061] Embodiment 3: system optimization

[0062] In order to simultaneously detect 24 types of HPV in the same reaction tube, the primer probe concentration and reaction system must be optimized to avoid interference between primer probes and the lower extension temperature required for Taqman probe hybridization .

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Abstract

The invention relates to a fluorescent PCR detection method for diagnosing human papilloma virus (HPV) infection, and a kit which is prepared according to the detection method and is used to detect HPV genotype of a DNA sample isolated from a patient body for diagnosing whether the HPV genotype belongs to one of the 24 types of human papilloma virus and determining as high risk, moderate high-risk and low risk, and belongs to the field of life science and technology. The method comprises: taking fluorogenic quantitative PCR as the technological basic polymerase chain reaction (PCR), employing the kit comprising multiple-type-directing forward primers, reverse primers and probes, and under specific PCR conditions and in a reaction tube, simultaneously detecting DNA of 24 types of HPV such as HPV 6, 11, 16, 18, 31, 33, 35, 39, 42, 43, 44, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 83, MM4 and cp8304. The kit and the detection method helps to simply accurately rapidly detect DNA of multiple types of HPV and reduce the cost, and is effectively applicable to prevention and screening of cervical cancers.

Description

[0001] Technical field: [0002] The invention relates to a fluorescent PCR detection method for diagnosing human papillomavirus (HPV) infection, and a kit made by using the method to detect HPV genotypes in DNA samples isolated from patients to diagnose whether they belong to the above-mentioned One of the 24 types is judged as high-risk, moderately high-risk, and low-risk types, which belong to the field of life science and technology. The method of the present invention includes a polymerase chain reaction (PCR) based on fluorescent quantitative PCR, including forward primers, reverse primers and probes for multiple types, which can be processed in a reaction tube under specific PCR conditions. Simultaneous detection of HPV6, 11, 16, 18, 31, 33, 35, 39, 42, 43, 44, 45, 51, 52, 53, 56, 58, 59, 66, 68, 73, 83, MM4 and cp8304 And so on 24 types of DNA. [0003] Background technique: [0004] Cervical cancer is the most common malignancy in women, mainly occurring in early ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/68G01N21/64
CPCC12Q1/70C12Q1/686C12Q2531/113C12Q2561/101
Inventor 孙益乐郭兴中吕校祥
Owner JIANGSU MOLE BIOSCI
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