Special probe and gene chip for identifying pathogenic candida
A Candida, pathogenic technology, applied in the field of special probes and gene chips for identifying pathogenic Candida
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Embodiment 1
[0040] Embodiment 1, detection of pathogenic candida and rapid identification of strains
[0041] Genomic DNA was extracted from samples of Candida known to contain different strains according to standard methods, and then the PCR reaction was carried out with the above-mentioned primer pair (sequence 13 and sequence 14 of the sequence table), and then the PCR product was mixed with different probes (respectively) The nitrocellulose membrane, which is the probe shown in sequence 1 to sequence 12), is subjected to a flow-through hybridization reaction with a medical nucleic acid molecular hybridization instrument, and the Candida species in the tested sample is determined according to the reaction result, and the required time is 6 hours. The results are shown in Table 1.
[0042] Table 1 Identification results of common pathogenic Candida
[0043] sample
Embodiment 2
[0044] Embodiment 2, detection of pathogenic Candida mixed bacteria and rapid identification of strains
[0045] Genomic DNA was extracted from samples containing known pathogenic Candida mixed bacteria according to standard methods, and then PCR reactions were carried out with the above-mentioned primer pair (sequence 13 and sequence 14 in the sequence table), and then the PCR products were mixed with different probes labeled (respectively the probes shown in sequence 1 to sequence 12) carry out the diversion hybridization reaction through the medical nucleic acid molecular hybridization instrument, and the mixed candida species present in the tested sample can be judged according to the result of the reaction, so The time required is 6 hours. The results are shown in Table 2.
[0046] Table 2 Identification results of common pathogenic Candida
[0047] specimen
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