Hepatitis B virus multi-drug resistant gene locus typing detection kit
A hepatitis B virus and detection kit technology, applied in the field of biotechnology detection, can solve the problems of cumbersome operation of detection technology, and achieve the effects of reducing the number of drugs, large clinical application value, and simple operation.
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Embodiment 1
[0043] The detection method steps of hepatitis B virus multi-drug resistance gene loci typing are as follows:
[0044] 1. Hepatitis B virus DNA extraction
[0045] Prepare 100 μL of serum containing hepatitis B virus, add 100 μL of concentrated solution, and centrifuge at 12,000 rpm for 10 minutes; discard the supernatant; add 25 μL of lysis buffer to mix, and lyse at 100°C for 10 minutes; finally, centrifuge at 12,000 rpm for 10 minutes, and the supernatant is the hepatitis B used sample.
[0046] 2. PCR reaction: the extracted DNA is amplified by PCR: the PCR primers used are two pairs of forward primers and reverse primers,
[0047] Forward primer 1CTACCAGCACGGGACCATGC
[0048] Reverse primer 1CAAGATGTTGTACAGACTTGG
[0049] Forward primer 2GTCCCTTTTTACCTCTATTACCA
[0050] Reverse primer 2TACATGCATATAAAGGCATTGAGG
[0051] The components of the PCR system are shown in the table below:
[0052] Reagent
concentration
System μL
ddH2O
9.1
...
Embodiment 2
[0065] Composition and preparation of reagents of hepatitis B virus multi-drug resistance gene loci typing detection kit
[0066] 1. Hepatitis B virus DNA extraction reagent, conventional method of concentration and cracking of hepatitis B virus.
[0067] 2. PCR reagents: see the table below
[0068] Reagent
concentration
sample system
µL
positive control
µL
negative control
µL
ddH2O
9.1
9.1
11.1
polymerase buffer
10×
2
2
2
Mgcl2
50mM
2.4
2.4
2.4
dNTP
10mM
2
2
2
polymerase
2U / μL
0.5
0.5
0.5
case sample
10 3 -10 7 drops
Spend
2 (sample)
2 (plasmid)
Primer
2mM
2
2
2
[0069] PCR reaction program: denaturation and enzyme activation at 95°C for 15 minutes, denaturation at 94°C for 15 seconds, annealing at 50°C for ...
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