Markers used for diagnosis of delayed preeclampsia
A preeclampsia and marker technology, applied in the field of markers for the diagnosis of delayed preeclampsia, can solve the problems of low sensitivity and less research, and achieve the effect of convenient material collection and avoiding medical waste.
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Embodiment 1
[0052] Example 1: Screening of novel diagnostic markers
[0053] Search a preeclampsia peripheral blood blood cell expression microarray database in Gene Expression Omnibus (GEO) (GSE48424) [16] , respectively compare different types of preeclampsia with the corresponding control group to screen differentially expressed genes ((Fold Change≥2; P-valuefigure 1 , the number of differentially expressed genes in early-onset preeclampsia was significantly lower than that in late-onset preeclampsia, and there was also heterogeneity among late-onset preeclampsia with different severity, such as figure 2 .
[0054] In order to further screen the genes that play a pivotal role in the onset of preeclampsia, we screened the genes in the microarray data for highly variable genes and performed correlation analysis, and divided them into 18 different modules, such as image 3 , there are mainly salmon, red, yellow, green, magenta, turquoise, black, blue and other modules.
[0055] Through...
Embodiment 2
[0058] Example 2: Detection of markers
[0059] 1) Take 2ml of venous blood with EDTA anticoagulant tube, and mix it upside down.
[0060] 2) Divide 2mL of peripheral blood into two 2mL EP tubes, 1mL each, 1500×g, 5min, 4°C;
[0061] 3) Add 1mL of PBS to the remaining blood cells, mix well to wash the cells, 1500×g, 5min, 4°C;
[0062] 4) Discard the supernatant, add 1 mL of TRIZOL (Invitrogen, 15596026) to the remaining blood cells, and mix well;
[0063] 5) After inverting and mixing, place it at room temperature for 10 minutes, add 200ul chloroform, vortex and mix thoroughly, and place it on ice for 5 minutes; 15000×r, 15 minutes, 4°C;
[0064] 6) Carefully pipette the supernatant into a new 1.5mL EP tube, add an equal amount of isopropanol to mix, and place at -20°C for 30min+;
[0065] 7) 15000×r, 5min, 4°C, pour the supernatant, add 1mL of pre-cooled 75% ethanol, blow and mix well;
[0066] 8) 15000×r, 5min, 4°C, repeat step 7 once;
[0067] 9) Pour the supernatant,...
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