Human MTHFR and MTRR gene detection kit and application thereof
A detection kit and gene detection technology, applied in the biological field, can solve the problems of prolonged diagnosis time, low sensitivity, cumbersome and time-consuming operation, etc., and achieve the effects of strong repeatability, simple operation, and rapid and objective detection results.
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Embodiment 1
[0043] Assembly of human MTHFR and MTRR gene detection kits
[0044] The kit includes the following components:
[0045] (1) Nucleic acid amplification reaction solution:
[0046] The nucleic acid amplification reaction solution is composed of RNase-free water, 10×PCR buffer, 25mM Mg 2+ , 10mM dNTPs composition (Table 1).
[0047] The composition of table 1 nucleic acid amplification reaction solution
[0048] Reagent name
Adding volume (μL) / 50 servings
PCR buffer
100
MgCl 2
3
100mM dATP
2.5
100mM dGTP
2.5
100mM dCTP
2.5
100mM dUTP
1.25
100mM dTTP
1.25
RNase-free water
337
total capacity
450
[0049] (2) Enzyme mixture
[0050] The enzyme mixture includes DNA polymerase, enzyme diluent and UDG enzyme. DNA polymerase plays a very important role in PCR amplification, including the efficiency and specificity of reverse amplification. In order to achieve bett...
Embodiment 2
[0079] Adopt the test kit of the embodiment of the present invention 1 to the detection test of clinical sample
[0080] 1. Sample processing (whole blood sample extraction)
[0081] 200 μL of whole blood samples were taken, and Qiagen Whole Blood Genomic DNA Extraction Kit (QIAamp DNA BloodMini Kit, Cat No.: 51104) was used to extract according to the kit instructions to obtain sample DNA.
[0082] 2. Reagent preparation
[0083] The kit prepared in Example 1 was used to prepare the reaction system (Table 7):
[0084] Table 7 Reaction system configuration table
[0085] reaction system
Dosage (μL) / 1 person
Nucleic Acid Amplification Reaction Solution
9
Enzyme Mix
1
Detection solution
8
sample DNA
2
total capacity
20
[0086] 3. PCR amplification program
[0087] Perform RT-PCR amplification according to the following procedure: amplification (37°C for 5min; 95°C for 15min; 95°C for 10s, 55°C for 40s...
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