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

Amplification composition and rapid detection kit used for trisomy 21 syndrome detection

A technology of trisomy 21 and detection kits, applied in the field of biotechnology detection, can solve the problems of insufficient detection efficiency and accuracy, unreasonable STR sites, and inability to take care of themselves in life, and achieve stable detection results and detection cycle. Short, objective and accurate results

Active Publication Date: 2013-06-26
BEIJING MICROREAD GENE TECH
View PDF5 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Children with trisomy 21 often have symptoms such as growth retardation, physical and intellectual disabilities, and inability to take care of themselves. Their living conditions are poor and they cause a great burden to the family.
The above-mentioned patents often use unreasonable or small number of STR sites, and the number of sites contained in each QF-PCR amplification system is small, resulting in insufficient detection efficiency and accuracy

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
  • Amplification composition and rapid detection kit used for trisomy 21 syndrome detection
  • Amplification composition and rapid detection kit used for trisomy 21 syndrome detection
  • Amplification composition and rapid detection kit used for trisomy 21 syndrome detection

Examples

Experimental program
Comparison scheme
Effect test

2 example 21 3

[0074] The following is the specific implementation of the detection of DNA samples from 2 cases of trisomy 21 patients and 1 case of normal persons by using the present invention.

[0075] 1. DNA extraction

[0076] Chelex-100, DNA extraction kit (Tiangen Biochemical) was used for DNA extraction. The operation steps were in accordance with the instructions. After DNA extraction, it was quantified with an ultraviolet spectrophotometer and diluted to 2ng / μl.

[0077] 2. PCR

[0078] 2.1 Reaction system:

[0079] Dissolve a total of 12 pairs of primers at Penta E and FGA sites and 10 STR sites on chromosome 21 to form a working solution with a concentration of 10μM, and then make a primer mix according to the volume ratio in Table 2: Primer See the sequence table in the appendix for the sequence.

[0080] Table 2 The volume ratio of each primer

[0081] Site name

Volume (μl)

D21S1437

2.0μl

D21S2052

0.6μl

D21S11

1.6μl

D21S2055

1.5μl

D21S1411

1.6μl

D21S1432

0.6μl

D21...

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 relates to a PCR (polymerase chain reaction) amplification composition and rapid detection kit used for trisomy 21 syndrome detection. Ten short tandem repeat sequences (D21S1437, D21S2052, D21S11, D21S2055, D21S1411, D21S1432, D21S1435, LFG21, Penta D and D21S1413) on a chromosome 21 and two non-short tandem repeat sequences (Penta E and FGA) on the chromosome 21 are amplified at the same time in one PCR system. The PCR amplification composition and rapid detection kit system can be used for diagnosing numerical abnormalities of a chromosome 21 of human, the obtained product is provided with fluorescent marks as each locus adopts a primer marked by fluorescence, detection can be carried out on instruments such as a genetic analysis meter, the obtained fragment length is more accurate, and repeatability is higher. The PCR amplification composition and rapid detection kit used for trisomy 21 syndrome detection have the advantages that operation is easy, large-scale popularization is convenient, the whole process is automatic, and the whole detection process can be completed by about six hours only.

Description

Technical field [0001] The present invention relates to the field of biotechnology detection, in particular to a PCR amplification composition for trisomy 21 detection, involving 10 pairs of specific primers and a rapid detection kit thereof. Background technique [0002] Down's syndrome, also known as Trisomy 21 syndrome, is a disease caused by an increase in the number of chromosome 21. It is the most common chromosomal disease in humans. It was first reported by British doctor Langdon Down in 1866. Have done a clinical description, so it is called Down syndrome. The incidence of live births is about 1 / 600-1 / 800, and the total prevalence of trisomy 21 in my country is 0.47‰, of which 0.26‰ in urban areas and 0.56‰ in rural areas (Zhang Zhixiang et al., Trisomy 21 in China Epidemiological study of symptom, "Chinese Journal of Clinical Psychology", 1996 03). Children with trisomy 21 often have symptoms such as growth retardation, physical and intellectual impairment, and inabili...

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
IPC IPC(8): C12Q1/68C12N15/11G01N21/64
Inventor 陈初光吕悦心宋欣欣
Owner BEIJING MICROREAD GENE TECH
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