9 microRNA markers for predicting whether primary liver cancer relapses
A primary liver cancer, sequence technology, applied in the direction of DNA / RNA fragments, recombinant DNA technology, the use of vectors to introduce foreign genetic material, etc., can solve the problem that the role cannot be underestimated
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[0074] The preparation of the miRNA chip can adopt conventional manufacturing methods of biochips known in the art. For example, if the solid phase carrier is a modified glass slide or silicon wafer, and the 5' end of the probe contains amino-modified poly dT strings, the oligonucleotide probe can be formulated into a solution, and then spotted with a spotting instrument. The miRNA chip of the present invention can be obtained by arranging in a predetermined sequence or array on a modified glass slide or a silicon chip, and then fixing it by standing overnight. If the nucleic acid does not contain amino modification, its preparation method can also refer to: "Gene Diagnosis Technology-Non-radioactive Operation Manual" edited by Wang Shenwu; J.L.erisi, V.R.Iyer, P.O.BROWN. Exploring the metabolic and genetic control of gene expression on agenomic scale.Science, 1997; 278:680 and Ma Liren, edited by Jiang Zhonghua. Biochip. Beijing: Chemical Industry Press, 2000, 1-130.
[0075...
Embodiment 1
[0094] The preparation of embodiment 1 RNA sample
[0095] Tissue sample:
[0096] 23 pairs of cancer and paracancerous tissues (including 10 samples with recurrence and 13 samples without recurrence) were obtained from surgical resection specimens of patients with primary liver cancer (HCC). These specimens were obtained from the First Affiliated Hospital of Zhejiang University and Qidong Liver Cancer Research Place. All the above-mentioned specimens were obtained with the approval of the ethics committee of the WHO partner organization authorized by the Shanghai Municipal Government. The clinical data of tissue samples include: gender, age, tumor size, pathological grade (Edmonson), liver cirrhosis, metastasis, recurrence, HBV and HCV infection, etc. All patients did not receive chemotherapy before operation, and the postoperative follow-up was up to 60 months.
[0097] Gene chip:
[0098] The microRNA expression profiling chip adopts the miRNA expression profiling chip ...
Embodiment 2
[0104] Extraction and labeling of embodiment 2microRNA
[0105] The miRNAs were extracted with Ambion's miRNAs extraction kit, and the specific operations were performed according to the corresponding instructions. Samples were labeled with T4 RNA ligase according to Thomson's method. In short, here's how:
[0106] 1.4 μg small RNA and 500ng 5'-phosphate-cytosine-uracil-cy3-3' (Dharmacon, Chicago, USA) and 2 units of 2units T4 RNA ligase (NEB, Ipswich, USA), incubated at 4°C for 2 hours , to label the miRNA. An equal amount of corresponding negative control was set up for each miRNA sample.
[0107] 2. The labeled RNA was precipitated with 0.3M sodium acetate and 2.5 volumes of ethanol, and then resuspended with 15 μl of hybridization solution containing 3×SSC, 0.2% SDS and 15% formamide. All hybridizations were repeated twice, and the hybridization was performed with LifterSlip TM (Erie, PA USA) to ensure that the hybridization solution flows evenly between the chip and t...
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