Apple virus detection test strip and preparation method thereof
A technology for detecting apple virus and test strips, applied in biochemical equipment and methods, methods based on microorganisms, measurement/inspection of microorganisms, etc., can solve problems such as operator poisoning, achieve high sensitivity, low detection limit, and molar absorption The effect of high coefficient
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[0042] ⑤Preparation of 20×SSC
[0043] The preparation method of 20×SSC: Weigh 8.76g NaCl and 4.41g trisodium citrate, add 45mL deionized water, and then adjust the pH value to 7.0 with dilute hydrochloric acid;
[0044] Preparation of 1×ExoIIIbuffer
[0045] The preparation method of 1×ExoIIIbuffer: 10×ExoIIIbuffer (purchased from Bao Biological Engineering (Dalian) Co., Ltd., 500mMTris-HCl, pH8.0, 50mMMgCl 2 , 10mMDTT) diluted 10 times, that is, take 5μL of 10×ExoIIIbuffer and add it to 45μL of water to obtain 1×ExoIIIbuffer, which consists of 50mMTris-HCl, pH8.0, 5mMMgCl 2 , 1mMDTT.
[0046] The DNA sequence used in the test in the examples of the present invention is as follows, synthesized by Takara Company and purified by HPLC. All solutions were prepared with ultrapure water (resistance of 18.2MΩ.cm).
[0047] ①Specific DNA probe 1
[0048] AuNPs-SH-5'-AAAAAA ACGAAGTCATCA AAAAAAA-3'
[0049] ② DNA probe 2
[0050] 5'-AGAGTTGTGTTTGGAGGA-3'
[0051] ③ DNA prob...
Embodiment 1
[0059] A kind of apple virus detection test strip of the present invention, as figure 1 As shown, it consists of a strip bottom plate, sample pads overlapped sequentially on the strip bottom plate, a gold label conjugate pad coated with specific DNA probe 1, a specific coated nitrocellulose membrane and an absorbent pad. One end of DNA probe 1 is combined with nano gold, and the nitrocellulose membrane is covered with a linear detection line T line coated with DNA probe 2 and a linear quality control line C line coated with DNA probe 3, such as figure 1 As shown, a large number of single-stranded DNAs (sequences 4 and 2*) were obtained through the circular amplification principle of targeted priming and ExoIII cleavage in the apple virus liquid to be tested. Probe 2 is complementary.
[0060] 1. Preparation of sample pad
[0061] Prepare 0.01mol / LTris-HCl buffer solution, wherein the Tris-HCl buffer solution contains 0.2% by mass of Tritonx-100, the concentration of NaCl is ...
Embodiment 2
[0073] 1. The preparation of the sample pad, the preparation of the gold-labeled conjugate pad coated with specific DNA probes, and the preparation of the specific coated nitrocellulose membrane are the same as in Example 2
[0074] 2. Collect samples of apple mosaic virus-positive plants and virus-free plants preserved by Yantai Academy of Agricultural Sciences, and use liquid nitrogen quick-frozen grinding and plant RNA extraction kits to extract total RNA from apple leaves.
[0075] 3. Preparation of tested single-stranded DNA
[0076] Convert 10 μmol / L structure to 5'-TCCTCCAAACACAACTCTTGATGACTTCGTAGAGTT
[0077] Heat the hairpin DNA of GTGTTTGGAGGAGCTTCCCACTGCCAACCT-3' at 95°C for 10 minutes, cool naturally, heat the actual apple virus liquid at 95°C for 10 minutes, and immediately put it in an ice bath, and then hybridize 2.5 μL of 500 nM hairpin DNA with 2.5 μL of the apple virus liquid extracted above to be tested in 45 μL 1×ExoⅢ buffer, reacted in 37°C water bath for...
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