Application of biomarker in diagnosis of Parkinson
A technology of biomarkers and uses, applied in UROD. , The application field of biomarkers in the diagnosis of Parkinson's can solve the problems of affecting, interfering with functional independence, interfering with daily life functions, etc., and achieve the effect of improving the quality of life
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Embodiment 1
[0050] Example 1 Screening for biomarkers related to Parkinson's
[0051] 1. Sample collection
[0052] 10 normal blood samples and blood samples from Parkinson's patients were collected, and all the above samples were obtained with the consent of the ethics committee.
[0053] Exclusion criteria for normal control group: (1) Parkinson's disease and family history of Parkinson's disease; (2) Alzheimer's disease. History of epilepsy, cerebrovascular disease and other neurological diseases; (3) previous history of mental illness. Such as schizophrenia, severe depression, mental retardation and mental disorders caused by physical diseases; (4) those who are illiterate, color blind, language barrier or unable to communicate due to other reasons.
[0054] Exclusion criteria for Parkinson's disease group: (1) People who are illiterate, color blind, language barrier or unable to communicate due to other reasons; (2) People with cognitive impairment or dementia caused by drug poison...
Embodiment 2
[0082] Example 2 QPCR sequencing to verify differential expression of UROD gene
[0083] 1. According to the detection results of high-throughput sequencing, the UROD gene was selected for large-sample QPCR verification. According to the sample collection method in Example 1, 80 cases of blood from Parkinson's patients and blood from normal people were selected.
[0084] 2. The RNA extraction steps are the same as in Example 1.
[0085] 3. Reverse transcription: use the reverse transcription kit from TIANGEN Company, the kit number is KR106. Specific steps are as follows:
[0086] To remove genomic DNA reaction, add 5×DNA Buffer 2.0μl, RNA 1μg to the test tube, add RNase-removing ddH 2 O Bring the total volume to 10 μl, heat in a water bath at 42°C for 3 minutes, then add 2.0 μL of 10×Fast RT Buffer, 1.0 μL of RTEnzyme Mix, 2.0 μL of FQ-RT Primer Mix, and remove RNase ddH 2 O 5.0 μL, mixed and added to the above test tube and mixed together, heated in a water bath at 42°C ...
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