Diagnosis kit for mycobacterium species identification and drug-resistance detection and mfg. method thereof
A diagnostic kit, mycobacteria technology, applied in the direction of biochemical equipment and methods, microbial measurement/inspection, specific-purpose bioreactor/fermenter, etc., can solve the problem of time-consuming and limited enzyme treatment steps
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Embodiment 1-1
[0049] Example 1-1: Mycobacterium Genomic DNA
[0050] The Department of Respiratory Diseases, Asan Medical Center (Seoul, South Korea) provided sequenced mycobacterial genomic DNA extracted from 10 clinical isolate cultures, and other mycobacterial genomic DNA was obtained from ATCC (Manassas, VA USA).
Embodiment 1-2
[0051] Example 1-2: Preparation of oligonucleotide probes and primers
[0052] Table 2 shows the sequences of the nucleotide probes and primers. Each of the biotin-TR8 and TR9 and probes used were custom-synthesized by Bionics (Seoul, South Korea), and all other reagents were first-class .
[0053] [Table 2]
[0054] According to the order shown in Table 2, select SEQ ID NO 1-40.
[0055] As shown in Table 2, the oligonucleotide chip designed for the study of rpoB gene point mutations included 7 wild-type probes, 17 RIF-resistant probes, and 8 RIB-sensitive probes.
[0056] The structure shows that 17 RIF resistance probes SEQ ID NO 20-36 can distinguish the mutations of the following codons: codon 511 (Leu>Pro), codon 513 (Gln>Pro), codon 516 (a:Asp> Val, b: Asp>Tyr, c: Asp>Glu), codon 518 (Asn>His), codon 521 (Leu>Met), codon 522 (Ser>Leu), codon 526 (a: His) Tyr, b: His) Asp, c: His) Arg, d: His) Asn, e: His) Ala, f: His>Cys, g: His) Gln, h: His> Gly), and codon 531...
Embodiment 1-3
[0062] Embodiment 1-3: the preparation of oligonucleotide chip
[0063] Fig. 1 is the flow chart of the preparation steps of the oligonucleotide chip that is used to construct the oligonucleotide chip of mycobacterium DNA identification among the present invention, as shown in Figure 1, the preparation step of this oligonucleotide chip comprises: the first step (10), Modify each mycobacterium composite probe: make the mycobacterium species identification probe containing the mycobacterium species-specific DNA sequence of the mycobacterium rpoB gene, the mycobacterium drug resistance detection probe containing one or more mycobacterium rpoB gene modification codons Needles, and control probes corresponding to the respective drug resistance detection probes composed of wild-type sequences, so that the 5' end contains an amine group; the second step (20), introduces an aldehyde group on the silanized glass slide and the third step (30), using Schiff base reaction to immobilize ...
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