A kind of human herpesvirus type 4 detection kit and detection method
A human herpes virus and detection kit technology, which is applied in the biological field, can solve the problems of nucleic acid samples containing many impurities, affecting the detection accuracy of the kit, and low extraction efficiency, and achieves the improvement of nucleic acid extraction rate, high accuracy and reduction of production. cost effect
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Embodiment 1
[0028] Embodiment 1, a kind of human herpes virus type 4 detection kit
[0029] Embodiment 1 of the present invention comprises the following components:
[0030] ①Nucleic acid release agent: add surfactant peptide to sterile water to make the final concentration reach 0.2mg / ml, add chlorhexidine acetate to make the final concentration reach 0.03mg / ml, add potassium chloride to make the final concentration reach 4.5% (w / v ) and adding hydrophilic graphene to make the final concentration reach 1.2% (w / v).
[0031] The preparation method of hydrophilic graphene: take the graphite oxide prepared by the Hummers method that has removed residual ions after dialysis, and prepare an aqueous solution of 0.5 mg / ml, according to the quality of graphite oxide: hexamethylenetetramine is 2: 1 Hexamethylenetetramine was added, stirred and refluxed at 100°C for 12 hours, and a uniformly dispersed hydrophilic graphene dispersion was obtained.
[0032] ②Nucleic acid extraction solution contai...
Embodiment 2、 Embodiment 1
[0042] Embodiment 2, the method for detecting EBV with the kit described in embodiment 1
[0043] 1. Preparation of samples to be tested
[0044] Preparation of serum samples: select freshly drawn venous blood, place it at room temperature for 25-35 minutes, centrifuge at 2000 rpm / min for 2-4 minutes, absorb the supernatant, and transfer it to a clean EP tube for later use.
[0045] 2. Nucleic acid extraction
[0046] A) Lyse the virus: Take four centrifuge tubes and add 6 μl nucleic acid release agent and 12 μl of the sample to be tested prepared in step 1), 6 μl nucleic acid release agent and 8 μl EBV negative control, 6 μl nucleic acid release agent and 8 μl EBV positive control, and 6 μl Nucleic acid release agent and 8 μl EBV quantitative reference substance, marked, mixed thoroughly, placed at room temperature for 3 minutes, set aside;
[0047] B) Magnetic bead adsorption: Add 100 μl of nucleic acid extraction solution containing magnetic beads and 4 μl of internal sta...
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