RT-PCR primers for detecting transcriptional level of NOX1 mRNA in serum as well as kit and method for evaluating concurrent intestinal cancer susceptibility of hyperglycemia population
A RT-PCR, transcription level technology, applied in DNA/RNA fragments, biochemical equipment and methods, recombinant DNA technology, etc., can solve the problems of inaccurate mRNA quantification, easy contamination, false positive rate, application limitations, etc.
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[0074] In the following, the present invention will be further described in conjunction with embodiments. However, it should be clear that the above description and the following examples herein are only used as examples and do not constitute a limitation on the scope of the present invention.
[0075] The experimental methods used in the following examples are conventional methods unless otherwise specified.
[0076] The materials and reagents used in the following examples can be obtained from commercial sources unless otherwise specified.
[0077] 1. Primer design and synthesis
[0078] 1.1 Design and synthesis of primers for NOX1 gene
[0079] The standard sequence of NOX1 gene to be amplified is 266-422 bases in the second and third exon regions of NOX1 gene, and primers are designed using the full-length mRNA sequence of NOX1 as a template. The sequence of the upstream primer F of the standard PCR is: 5'-ATAGCAGAAGCCGACAGG -3'; the sequence of the downstream primer R is: 5'-CC...
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