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
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[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...
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