Mycoplasma Nucleic Acid Isothermal Amplification Method
A technology for Mycoplasma genitalium and Mycoplasma genitalium, which is applied in the directions of biochemical equipment and methods, DNA/RNA fragments, microorganism determination/inspection, etc., can solve the problem that there is no research report on the real-time fluorescent nucleic acid isothermal amplification detection technology of Mycoplasma genitalium.
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Embodiment 1
[0249] Embodiment 1 is used for real-time fluorescent nucleic acid constant temperature amplification to detect the design of special primers and probes of Mycoplasma genitalium (MG)
[0250] The present invention selects no secondary structure and a highly conserved segment in the MG virus 16SRNA gene as the amplified target sequence region (its nucleotide sequence is shown in SEQ ID NO: 1), and according to the principle of primer probe design, DNAStar, DNAMAN Software and artificially designed special primers and probe sequences for real-time fluorescent nucleic acid constant temperature amplification detection of Mycoplasma genitalium (MG), and obtained the following specific sequences:
[0251] (1) a capture probe (TCO, Target Capture Oligo) that can specifically bind to the target nucleic acid (MG RNA) sequence of Mycoplasma genitalium (MG), the nucleotide sequence of the capture probe is: 5'TGCACACCGGATGGCCAATCCAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA3' (SEQ ID No.: 2);
[0...
Embodiment 2
[0258] Embodiment 2 is used for the design of special primers and probes of real-time fluorescent nucleic acid constant temperature amplification detection Mycoplasma pneumoniae (MP)
[0259] The present invention selects no secondary structure and a highly conserved segment in the MP virus 16SRNA gene as the amplified target sequence region (its nucleotide sequence is shown in SEQ ID NO: 10), and according to the principle of primer probe design, DNAStar, DNAMAN Software and artificially designed special primers and probe sequences for real-time fluorescent nucleic acid constant temperature amplification to detect Mycoplasma pneumoniae (MP), and obtained the following specific sequences:
[0260] (1) a capture probe (TCO, Target Capture Oligo) that can specifically bind to the target nucleic acid (MP RNA) sequence of Mycoplasma pneumoniae (MP), the nucleotide sequence of the capture probe is: 5'TGCACACCGGATGGCCAATCCAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA3' (SEQ ID No.: 2);
[026...
Embodiment 3
[0267] The real-time fluorescent nucleic acid constant temperature amplification detection kit of embodiment 3 Mycoplasma genitalium (MG)
[0268] Using the special primers and probes provided in Example 1, the real-time fluorescent nucleic acid constant temperature amplification detection kit for Mycoplasma genitalium (MG) of the present invention was obtained. The kit contains components such as capture probe (TCO, Target Capture Oligo), T7 primer, nT7 primer, MG detection probe, internal standard detection probe, internal standard, M-MLV reverse transcriptase and T7 RNA polymerase .
[0269] The capture probe exists in the nucleic acid extraction solution, the T7 primer, nT7 primer, MG detection probe, and internal standard detection probe exist in the MG detection solution, and the M-MLV reverse transcriptase and T7 RNA polymerase It exists in the SAT enzyme solution. Specifically, the kit is divided into A box (specimen processing unit) stored at 2-30°C and B box (nuclei...
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