Serum miRNA combination as molecular marker for assessing non-obstructive azoospermia
A molecular marker, non-blocking technology, applied in the direction of DNA/RNA fragment, recombinant DNA technology, microbial determination/inspection, etc., can solve the problems of weak correlation of fertilization ability, difficult standardization of semen, etc., to achieve high accuracy, Simple to use effects
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Embodiment 1
[0028] Example 1 Microarray detection of differential expression of miRNA in the serum of patients with non-obstructive azoospermia and healthy sperm donors
[0029] 1. Experimental group
[0030] Sample group: Serum samples from patients with non-obstructive azoospermia were obtained from Guangdong Provincial Family Planning Specialized Hospital, and were diagnosed as patients with non-obstructive azoospermia by the Andrology Department of our hospital;
[0031] Control group: Serum samples from healthy males who donated sperm to Guangdong Human Sperm Bank and met the conditions for donating sperm. The diagnostic criteria of non-obstructive azoospermia are azoospermia with no sperm found in two routine semen analyzes except for vas deferens obstruction factors.
[0032] 2. Experimental operation
[0033] The samples were collected with the consent of the Ethics Committee of the Guangdong Provincial Family Planning Specialty and after the patients’ informed consent.
[0034...
Embodiment 2
[0044] Example 2 Real-time quantitative PCR to verify the differential expression of miRNA in the serum of patients with non-obstructive azoospermia and healthy sperm donors
[0045]According to the results of the miRNA microarray chip, five miRNAs with higher Fold change (hsa-miR-1263, hsa-miR-221-5p, hsa-miR-483-3p, hsa-miR-4275 and hsa-miR-194 -3p), using Mir-X TM miRNAqRT-PCR Kit for real-time quantitative PCR validation.
[0046] 1. Experimental operation
[0047] RNA was extracted and reverse-transcribed using Mir-X miRNA First-Strand Synthesis Kit. The primer for reverse transcription was: 5-GCTGTCAACGATACGCTACGTAACGGCATGACAGTG-3, and 5SrRNA was used as an internal reference gene. Others were carried out according to the instructions of the kit. The upstream primers used are listed in Table 2. The downstream primer used the 3' primer in the kit: 5-GCTG TCAACGATA CGCTACG TAA-3'.
[0048] The reaction was amplified on a 96-well STEPONEPLUS (ABI, USA) fluorescent P...
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