Gold shell magnetic nanoparticles, preparation thereof and use thereof
A technology of magnetic nanoparticles and gold nanoparticles, which can be used in magnetic materials, magnetic objects, biochemical equipment and methods, etc., can solve problems such as difficulty in cellulase detection, and achieve improved bioaffinity, huge application potential, good The effect of bioaffinity
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Embodiment 1
[0034] A gold-shell magnetic nanoparticle of the present invention, which is prepared through the following steps (the process flow of the following steps can be found in figure 1 ):
[0035] 1. Preparation of silicon shell magnetic core nanoparticles
[0036] 8.5g FeCl 3 ·6H 2 O and 3g FeCl 2 4H 2 O was dissolved in 38mL 0.4M hydrochloric acid, then poured into 375mL 0.7M ammonia water filled with nitrogen, and stirred vigorously at room temperature to form Fe 3 o 4 Colloidal precipitation, washed three times with water to obtain magnetic nanoparticles and suspended in 150mL of water, take 20mL of the suspension and add it to 200mL of isopropanol and mix thoroughly, then add 5.36g of PEG, 20mL of water, 10mL of ammonia (28%) and 1.2mL TEOS, stirred at room temperature for 24h, ultrasonically cleaned the product twice with ethanol and water, and freeze-dried to obtain silicon-shell magnetic core nanoparticles.
[0037] 2. Preparation of gold seed-silicon shell magnetic ...
Embodiment 2
[0045] The gold-shell magnetic nanoparticles prepared in the above-mentioned Example 1 were applied to the detection of cellulase gene, which specifically refers to the function of encoding cellobiohydrolase (produced by Trichoderma reesei) two subtype components Gene (cbh2), the specific operation method of the detection application includes the following steps:
[0046] 1. Design of oligonucleotide strand probe and target strand
[0047] According to the gene coding sequence of cbh2, the oligonucleotide probe, target strand and two-base mismatched strand of cbh2 were designed by Primer Premier 5 software, and Oligo 6 software and NCBI website (http: / / www.ncbi.nlm. The Blast resources in nih.gov / BLAST / ) further screened the probes, and selected the optimal probes and target strands for synthesis, and their sequences are shown in Table 1 below.
[0048] Table 1: Sequences of oligonucleotide probes, target strands and two-base mismatch strands of cbh2
[0049] Oligon...
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