Primers, probe and kit for detecting JCV (JC virus)
A JC virus and kit technology, applied in the field of probes and kits, and primers for detecting JC virus, can solve problems such as inaccurate antibody detection, and achieve the effects of improving sensitivity, avoiding subjectivity, and reliable detection results
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Embodiment 1
[0033] Example 1. A primer and fluorescent probe for the quantitative detection of JC virus nucleic acid
[0034] The embodiment of the present invention provides a primer and a probe for detecting JC virus. The primer and probe include: a forward primer for detecting JC virus, a reverse primer for detecting JC virus and a primer for detecting JC virus. probes, where,
[0035] The forward primer used to detect JC virus is shown in SEQ ID NO.1 in the sequence listing;
[0036] The reverse primer used to detect JC virus is shown in SEQ ID NO.2 in the sequence listing;
[0037] The probe for detecting JC virus is shown in SEQ ID NO.3 in the sequence listing;
[0038] The 5' end of the probe is connected with a fluorescent group FAM, HEX, TET, JOE, VIC, ROX, Cy3 or Cy5, and the 3' end of the probe is connected with a quencher group TAMRA, Eclipse, BHQ1, BHQ2, BHQ3 or DABCYL . In the embodiment of the present invention, the fluorescent reporting group of the probe is FAM, the e...
Embodiment 2
[0043] Embodiment 2. A kind of kit for detecting JC virus
[0044] The embodiment of the present invention provides a kit for detecting the quantitative nucleic acid of JC virus. The kit includes the primers and probes provided in Example 1 of the present invention. Positive controls, positive controls, negative controls, and working standards.
[0045]Specifically, each component of the PCR reaction solution includes in the PCR amplification reaction system: Taq enzyme with a final concentration of 0.01U / μL-0.05U / μL, dNTPs with a final concentration of 0.2-0.6mM, 10×PCR buffer and A solution containing Mg ions at a final concentration of 1.5-5.0 mM. In this example, the ratio of the contents of each component of the PCR reaction solution is: 0.3 μL of Taq enzyme at a concentration of 5 U / μL, 2 μL of dNTPs at a concentration of 10 mmol / L, 5 μL of 10×PCR Buffer and 25 mmol / L MgCl 2 Solution 5 μL.
[0046] Specifically, the final concentrations of the forward primer and the ...
Embodiment 3
[0079] Embodiment 3. A kind of kit for detecting JC virus
[0080] The embodiment of the present invention provides a kit for detecting JC virus nucleic acid in a sample. The components of the kit differ from those in the kit provided in Example 2 in that:
[0081] The ratio of the contents of each component of the PCR reaction solution is: 0.1 μL of Taq enzyme at a concentration of 5 U / μL, 1 μL of dNTPs at a concentration of 10 mmol / L, 5 μL of 10×PCR Buffer and MgCl at a concentration of 25 mmol / L 2 Solution 3 μL.
[0082] Add 0.25 μL each of forward primer and reverse primer with a concentration of 10 μmol / L, and add 0.25 μL of probe with a concentration of 10 μmol / L.
[0083] During practical application, primers and probes can be added together into the PCR reaction solution, and then sterile water can be added to a volume of 10 μL.
[0084] The DNA extraction solution included Triton-X100 with a final concentration of 0.1%, NP-40 with a final concentration of 0.2% and T...
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