Immuno comb array test paper for detecting antibody of SIV (simian immunodeficiency virus) as well as preparation method and application
A technology for detecting test strips and viruses, which can be used in viruses/phages, biochemical equipment and methods, and biological testing.
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Embodiment 1
[0056] Design and synthesis of embodiment 1SOE-PCR primers
[0057] According to the gene sequence of monkey SIV virus, SOE-PCR amplification primers were designed using the principle of overlap extension PCR (SOE-PCR). The primer sequences are as follows:
[0058] SIVF: 5'-GAATTCTCAGAAGGCTGCACTCCCTATGACATCAATCAA
[0059] ATGCTAAATTGTGTATCAGA-3'
[0060] SIVR: 5’-CTCGAGTACACAATTTAGCATTTGATTGATGTCATAGGGAGTG
[0061] CAGCCTTCTGATACAC-3'
Embodiment 2
[0062] Cloning and sequencing of the simian SIV virus SIV30 gene of embodiment 2
[0063] (1) Cloning of SIV30 gene of monkey SIV virus
[0064] Carry out SOE-PCR with the primers designed and synthesized in Example 1, and the PCR reaction system is as follows:
[0065] The mixture was pre-denatured at 95 °C for 5 min, denatured at 94 °C for 1 min, annealed at 63 °C for 30 s, extended at 72 °C for 1 min, 30 cycles, and a total extension of 10 min at 72 °C.
[0066] The above mixture is as follows:
[0067] SIVF primers
2 μL
SIVR primers
2 μL
2×Taq MasterMix
15 μL
Ultra-pure water
Make up to 30 μL
[0068] PCR amplification results were detected by agarose gel electrophoresis, such as figure 1 As shown, it shows that the experiment obtained specific DNA fragments consistent with expectations.
[0069] (2) Recovery of PCR products
[0070] Overlap PCR amplification products were recovered with a DNA recovery kit. For spe...
Embodiment 3
[0073] The construction of embodiment 3 expression vector
[0074] pMD18T-SIV and pGEX-4T-1 were digested with EcoRI and XhoI respectively, and the digested target fragments were gel recovered. Connect the recovered target fragments, the connection system is as follows:
[0075] target segment
5 μL
pGEX-4T-1
2 μL
T4 DNALigase
1 μL
10×Ligase Buffer
1 μL
wxya 2 o
1 μL
[0076] Ligate overnight at 16°C.
[0077] The ligation product was transformed into BL21(DE3)pLysS competent cells, the positive colonies were screened by ampicillin resistance, and the plasmid was extracted for SmaⅠ and EcoRI double enzyme digestion identification. The result is as figure 2 shown. The positively identified plasmid was named pGEX-4T-SIV.
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