Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Human chromosome gene IL28B site polymorphism detection kit, and detection method and application thereof

A chromosomal gene, locus polymorphism technology, applied in biochemical equipment and methods, microbial determination/inspection, DNA/RNA fragments, etc. Insufficient site information and other problems can shorten the detection time, reduce production costs, and avoid inaccurate detection.

Inactive Publication Date: 2014-08-20
厦门安普利生物工程有限公司 +1
View PDF4 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] The above existing technologies all have uncertainty in the detection results, and at the same time, they can only detect polymorphic sites with insufficient information, and the detection process is complicated and has limitations.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Human chromosome gene IL28B site polymorphism detection kit, and detection method and application thereof
  • Human chromosome gene IL28B site polymorphism detection kit, and detection method and application thereof
  • Human chromosome gene IL28B site polymorphism detection kit, and detection method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0077] 1. Lysis: Take 100 μl of ethylenediaminetetraacetic acid (EDTA) tripotassium salt or sodium citrate anticoagulated whole blood from the patient to be tested (Xiamen Hospital of Traditional Chinese Medicine) and add it to a 1.5ml centrifuge tube, then add 200 μl of lysis buffer (3M Melonium isothiocyanate, 10 mM EDTA, 1% Triton-X100, 20 mM Tris-HCl (pH6), 20 μl proteinase K, mixed evenly, and heated at 55° C. for 10 min. 2. Magnetic adsorption, add 10 μl magnetic nanoparticles (Shanghai Aorun Micro-Nano New Material Technology Co., Ltd. SM-015D) to the above centrifuge tube, mix well and let it stand for 10 minutes, place it on a magnetic stand for magnetic separation, and absorb the waste liquid , suck as much as possible. 3. For washing, add 300 μl washing solution (1.5M NaCl, 0.5% Triton-X100, 10mM EDTA, 20mM Tris-HCl pH6) to the above centrifuge tube, shake and mix well, put it on a magnetic adsorption rack, solidify the magnetic particles, and absorb waste liquid. ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides a human chromosome gene IL28B site polymorphism detection kit, and a detection method and application thereof. The kit comprises at least one group of primers and probes in group a, group b and group c. The primers and the probes comprise: a: 860L1, 860L2, 860R, 860P; b: 275L1, 275L2, 275R, 275P; and c: 917L1, 917L2, 917R, 917P. 5' terminals of 860P, 275P and 917P are labeled as FAM, and 3' terminals are labeled as DACYL. The invention also discloses the detection method and application of the kit. The method is relatively simple and rapid, and is easy for realizing whole-course automation; secondary pollution of PCR products is avoided, and pollution is reduced; the cost is relatively low and relatively economic; and present popularized equipment in the market can be utilized, and no new investment is needed.

Description

technical field [0001] The invention relates to an in vitro diagnostic reagent, in particular to a detection kit for the polymorphism of the human chromosome gene IL28B site, a detection method and an application thereof. Background technique [0002] The polymorphisms of the host IL28B gene, and its closely related single nucleotide polymorphisms mainly include rs12979860, rs12980275, and rs8099917 located upstream of the IL28B gene on chromosome (19q13). [0003] At present, the detection methods of IL28B polymorphism mainly include gene sequencing (such as 201210234084.6 kit for detecting IL28B SNP12980275 polymorphism in patients with hepatitis C) and reverse hybridization (such as 201010019477.5 Hepatitis C virus genotyping and IL28 polymorphism). Both of these methods need to amplify the target gene first, and then detect the amplified product a second time, so the operation is complicated. At the same time, the gene amplification product is more than 100 million tim...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/68C12N15/11
CPCC12Q1/6858C12Q2531/113C12Q2535/137C12Q2563/107
Inventor 魏超魏劭
Owner 厦门安普利生物工程有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products