Kit for detecting 34 mutation sites of lung cancer based on MALDI-TOF-MS
A technology of mutation sites and kits, applied in recombinant DNA technology, microbial measurement/testing, DNA/RNA fragments, etc., can solve problems such as time-consuming, limited number of genes and sites, complex operations, etc.
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2018-08-17
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention relates to the technical field of lung cancer mutation site detection, and more specifically, to a kit for detecting 34 mutation sites in lung cancer based on MALDI-TOF-MS. Background technique
[0002] Lung cancer is one of the most common malignant tumors in the world today. Its tumor morbidity and mortality rate rank first in men and second only to breast cancer in women. Chemotherapy is currently the main method for the treatment of advanced lung cancer, and it is also one of the preoperative and postoperative adjuvant treatments for patients. Clinically, some patients have poor chemotherapy effect and chemotherapy failure. The main reason is that the tumor cells are not sensitive or resistant to anticancer drugs. Therefore, it is particularly important to understand the relevant factors of patients' drug sensitivity for individualized treatment of lung cancer patients and guidance for the application of targeted drugs.
[0003] It ...
Examples
Embodiment 1
[0134] 1. A kit for detecting 34 mutation sites in lung cancer based on MALDI-TOF-MS, said kit comprising: purified water, multiple PCR buffer, magnesium chloride buffer, dNTP mixture, multiple PCR enzyme, amplification primer mixture 1-2, phosphatase buffer, phospho-digesting enzyme, extension buffer, base extension reaction catalyzing enzyme, extension termination mixture A, T, C, G, extension primer mixture 1-8.
[0135] Wherein, the elongation termination mixture A, T, C, and G are all aqueous solutions of the mixture of four dideoxynucleotides, ddATP, ddTTP, ddCTP and ddGTP, wherein the ratio of the elongation termination mixture A is 1:4:4:4 , the ratio of extension-stop mixture T is 4:1:4:4, the ratio of extension-stop mixture C is 5:5:1:5, and the ratio of extension-stop mixture G is 3:3:3:1.
[0136] Multiplex PCR amplification reaction primers shown in SEQ ID NO: 1-14 constitute an amplification primer mixture 1;
[0137] The multiplex PCR amplification reaction pri...