Method and kit for detecting individualized medication related gene in tumor chemotherapy
An individual and gene technology, applied in the field of molecular biology, can solve the problems of low throughput, low resolution, high background signal, etc., and achieve the effect of reducing usage, simple and stable reagent consumables
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Embodiment 1
[0095] The design of embodiment 1 primer
[0096] (1) PCR amplification primers:
[0097] According to the individualized drug-related genes of the selected tumor chemotherapy individualized drugs to be detected, the amplification primers specific for each individualized drug-related gene are designed, and the amplification primers can amplify a segment including the mutation site. DNA sequence. The amplification primer has at least 15 bases at the 3' end that completely match the gene sequence it is targeting, and has a 10 base (acgttggatg) tag sequence at the 5' end to distinguish the amplification primer from the extension primer.
[0098] (2) Mass spectrometry extension primer:
[0099] Design an extension primer, the length of the extension primer is 15-28 bases, and its 3' end is located at the last base in the extension direction of the drug-related mutation site, and the extension primer only extends when the extension reaction occurs One base, the extended base is ...
Embodiment 2
[0115] The preparation of embodiment 2 detection template
[0116] Mutation samples are tumor tissues (numbered 2-A and 2-B) of 2 tumor patients in the hospital and 4 normal human tissue samples (numbered 3-A, 4-A, 5-A, 6-A) DNA was extracted (extracted using Tiangen DNA kit, and the operation method was extracted according to the instructions of the kit).
Embodiment 3
[0117] Example 3 Detection method of genes related to individualized medication of tumor chemotherapy
[0118] (1) Using the DNA extracted in Example 2 as a template, use the PCR amplification primers in Example 1 to amplify by PCR to obtain the target sequence amplification product. See Table 4 for the PCR amplification reaction system. Among them, all reagents were purchased from Agena Bioscience.
[0119] Table 4: PCR amplification reaction system
[0120]
[0121]
[0122] The PCR reaction conditions were 94°C for 2 minutes; denaturation at 94°C for 30 seconds, annealing at 56°C for 30 seconds, extension at 72°C for 1 minute, and a total of 45 cycles of amplification; finally, extension at 72°C for 5 minutes. In this example, the DNA extracted in Example 2 was used as the DNA template for PCR amplification. At the same time, sterile double distilled water was used as a negative control. The control sample and the test sample were reacted and tested according to t...
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