Application of adamts-2 gene and its expression product in diagnosis and treatment of gastric cancer
A technology for expressing products and genes, applied in the field of tumor markers, to achieve the effect of good application prospects, good stability and rapid response
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Embodiment 1
[0034] Example 1 Screening and analysis of GEO data
[0035] Restricting the study type to "expression profiling by array" datasets meeting the following criteria will be included in our study:
[0036] ①The selected data set must be the expression profile sequencing data of the whole genome;
[0037] ② These data come from the samples of gastric cancer case group and / or control group (without drug stimulation or transfection);
[0038] ③ This study considers standardized or original data sets.
[0039] Finally, 6 sets of microarray datasets were included in our study. The results are detailed in Table 1.
[0040] Table 1 Basic information of gastric cancer dataset
[0041]
[0042] All datasets were integrated to get 17481 genes. The probe IDs were converted to gene IDs according to the array annotations, the common genes of all expression profiles were screened, the missing data was filled for each set of expression profiles, and the data were normalized. Differenti...
Embodiment 2
[0043] The collection of embodiment 2 cases
[0044] All tissue samples were from gastric cancer patients diagnosed in the hospital from November 2012 to June 2014. When collecting materials, the central tissue of the cancer and the normal gastric mucosa tissue adjacent to the cancer were taken separately, and the specimens were quickly put into a small liquid nitrogen tank for preservation.
Embodiment 3
[0045] Example 3 extracts the total RNA in the sample
[0046] 1) Place the small pieces of sample tissue in a petri dish, add 1ml Trizol, cut it into pieces and move it to a homogenizer for homogenization;
[0047] 2) After the homogenization is completed, take out the homogenate and place it in an EP tube, set the volume to 1ml, and store it at -70°C;
[0048] 3) Place at 15-30°C for 5 minutes, add 200 μl chloroform, shake vigorously for 15 sec, and place at 15-30°C for 10 minutes;
[0049] 4) 2-8°C, centrifuge at less than 12000g / min for 10min, discard the supernatant, add 1ml of 75% ethanol, centrifuge at less than 7500g / min for 5min, discard the supernatant, and spot off;
[0050] 5) After the precipitate is dried (translucent, do not completely dry, otherwise the stability will be reduced), dissolve with RNase-freewater at 55-60°C, and freeze at -70°C.
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