A gene diagnosis kit for Parkinson's disease
A technique for gene diagnosis and Parkinson's disease, applied in the field of molecular biology, to reduce misdiagnosis rate and missed diagnosis
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Embodiment 1
[0045] Determination of the gene of embodiment 1, primer design and kit composition and amplification procedure
[0046] The 11 genes involved in the present invention are related to PD disease, and the correlation has been reported in the literature. The sequences of 11 genes can be obtained through the following ways.
[0047] The gene sequence can be retrieved at http: / / www.ncbi.nlm.nih.gov / pubmed according to the following gene ID
[0048] Table 1 Gene ID
[0049] Gene
gene ID
SNCA
6622
parkin
5071
UCHL-1
7345
Pink1
65018
DJ-1
11315
ATP13A2
23400
[0050] GIGYF2
26058
HTRA2
27429
FBX07
25793
Vps35
55737
MAPT
4137
[0051] The primers were designed according to the conserved regions of each gene, and the primers were used to specifically amplify all CDS regions of each gene. The forward and reverse primers were designed in the 5'-UTR and...
Embodiment 2
[0064] The gene diagnosis of embodiment 2 Parkinson's disease
[0065] Use the test kit of embodiment 1, carry out the application of embodiment 2, specifically carry out according to the following steps respectively:
[0066] In the Parkinson's disease genetic diagnosis kit provided by the present invention, the detection sample may be the blood, body fluid, hair, bone, cell or tissue specimen of the individual to be tested. In this example, the same standard cell line as in Example 1 was used.
[0067] 1. Extraction of individual human fibroblast skin cell RNA to be tested:
[0068] 1. Take the sample to be tested, add 1ml Trizol, mix on ice, mash and homogenate; let stand on ice for 10min;
[0069] 2. Add 200 μl chloroform to the homogenate, shake vigorously for 15 seconds, and incubate at room temperature for 10 minutes
[0070] 3.4℃, 12000g / min, centrifuge for 15min
[0071] 4. Take the water phase (upper layer), add 500 μl isopropanol, shake gently, and incubate at r...
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