Uc002mev.3 and in-vitro detection reagent, preparation or kit, application and detection method
An in vitro detection and kit technology, applied in biochemical equipment and methods, microbiological determination/inspection, DNA/RNA fragments, etc., can solve the problems of false elevation and achieve the effect of enriching research
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Embodiment 1
[0022] Example 1: A long-chain non-coding RNA uc002mev.3, the nucleic acid sequence of which is shown in SEQ ID No:1. The transcription region of the long-chain non-coding RNA uc002mev.3 (lncRNA uc002mev.3) described in this example is located on chromosome 19, with a starting position of 6,436,431-6,459,781 and a full length of 23,351 bp. The long-chain non-coding RNA uc002mev.3 described in this example can provide new blood biomarkers and therapeutic targets for the early diagnosis and prognosis monitoring of acute myocardial infarction, further enriching the research on the pathogenesis of acute myocardial infarction.
Embodiment 2
[0023] Example 2: As an optimization of the above example, the acute myocardial infarction-related gene is the full length of the long-chain non-coding RNA uc002mev.3.
Embodiment 3
[0024] Example 3: A reagent for detecting long-chain non-coding RNA uc002mev.3 in vitro, including a pair of specific primers for amplifying long-chain non-coding RNA uc002mev.3, the pair of specific primers includes upstream primers and downstream primers, upstream The sequence of the primer is shown in SEQ ID No: 2, and the sequence of the downstream primer is shown in SEQ ID No: 3. The expression level of lncRNA uc002mev.3 described in the present invention can be obtained by combining the reagents for in vitro detection of long-chain non-coding RNA uc002mev. The expression level of lncRNA uc002mev.3 can be used for screening of acute myocardial infarction. The specific primer pair described in this example is applicable to the detection of SYBRGreen, Taqman probes, molecular beacons, double-hybrid probes, and composite probes.
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