Fluorescence labeled human triple-negative breast cancer osseous metastasis cell line
A triple-negative breast cancer, fluorescent labeling technology, applied in the field of bioengineering, can solve the problems of the inability to visualize and trace the bone metastasis cell line, and achieve the effect of bone metastasis ability and bone metastasis specificity.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] The present invention provides a fluorescently labeled human triple-negative breast cancer bone metastases cell line, which is prepared by the following method:
[0029] (1) Culture parental human triple negative breast cancer cell MDA-MB-231 (purchased from ATCC);
[0030] (2) Amplify the lentiviral vector pLemiR (product of Open biosystems) containing the red fluorescent protein RFP. Using the method of transfecting cells with lentivirus, transfect MDA-MB-231 cells, and prepare MDA-MB-231 cells containing red fluorescent markers;
[0031] (3) Sorting by flow cytometry to obtain red fluorescent RFP-MDA-MB-231 cells ( figure 1 A: white light image of RFP-MDA-MB-231 cells, figure 1 B: fluorescence image of RFP-MDA-MB-231 cells);
[0032] (4) Transplant 1 million RFP-MDA-MB-231 cells into the fourth pair of mammary fat pads in nude mice. Tumors began to form after one week, and the tumor diameter reached 0.8-1.2cm after four to six weeks;
[0033] (5) Nude mice were k...
Embodiment 2
[0041] The MDA-MB-231-BM cells obtained in the present invention are tested for cell proliferation, cell migration, bone metastasis and tumorigenesis, and the gene expression characteristics of the MDA-MB-231-BM cells are tested. The experimental steps are as follows:
[0042] 1: Colony formation assay was used to detect cell proliferation ability.
[0043] 1) After digestion of MDA-MB-231 and MDA-MB-231-BM in good condition in logarithmic growth phase, add complete medium to make cell suspension;
[0044] 2) Count the cells of the cell suspension, inoculate 2,000 cells in a 12-well plate, add 1 mL of complete medium to the 12-well plate, and spread the cells evenly on the culture plate;
[0045] 3) Place the 12-well plate in the cell incubator, and change the medium every 2-3 days after the cells adhere to the wall to avoid contamination;
[0046] 4) When a round cell mass can be seen under the microscope (about the 10th day), take out the 12-well plate, discard the culture...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com