Method for early detection of cancer by using nematodes
An early detection and nematode technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve the problems of low cancer detection rate, high price, time-consuming and labor-intensive
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Embodiment 1
[0081] cancer detection
[0082] a. Breeding of nematodes
[0083] Five to six adults of wild-type nematode N2 were placed in a 6 cm petri dish (NGM medium coated with Escherichia coli), and cultured at 20° C. for 4 days. 300 to 500 adults of the next-generation nematodes were bred.
[0084] b. Analyzing Chemotaxis
[0085] In a 9cm Petri dish press figure 2 4 drops of 0.5ul sodium azide (NaN 3 ).
[0086] Add 1ml of washing buffer to the nematode feeding plate, and collect the floating nematodes with a test tube. Since the nematodes will sink after a little standing, discard the supernatant after the nematodes sink. Then add 1 ml of washing buffer to the test tube, discard the supernatant after the nematode sinks, repeat this process 3 times, and remove Escherichia coli.
[0087] 1 μl of urine samples diluted 10 times with sterile distilled water were dropped into the "+" parts of the 9 cm petri dish.
[0088] c. Place about 100 nematodes in the center of the petri dis...
Embodiment 2
[0093] In this example, although the sediment and solids in the urine were removed by centrifugation and filtration, this treatment had no effect on the chemotaxis of nematodes ( image 3 ).
Embodiment 3
[0095] In this embodiment, the established tumor cell line and the culture medium or storage solution are used as the model of the subject's living body-related substances to carry out the cancer detection experiment.
[0096] 1. Using tumor cell lines to detect cancer
[0097] To detect cancer using culture supernatants of human tumor cell lines, colon cancer (rectal cancer) cells of SE480, COLO201 and COLO205, breast cancer cells of MCF7, and gastric cancer cells of NUGU4, MKN1 and MKN7 were used.
[0098] SW480, COLO201, COLO205 and other cells were obtained from the Cell Resource Center of Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences. All cell lines used BPMI1640 medium with 10% FBS (fetal bovine serum), maintained at 37°C, 5% CO 2 Non-fused state under ventilated conditions. The culture medium of the clear layer above the culture medium was used in the experiment. The culture medium after culturing the cells was placed on the assay plate ( ...
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