A group of mutation gene groups and detection kits for assessing breast cancer risk
A detection kit, a technology for mutant genes, applied in the determination/inspection of microorganisms, recombinant DNA technology, DNA/RNA fragments, etc., can solve problems such as method limitations, and achieve high detection efficiency, fast detection speed, and high detection rate. Effect
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Embodiment 1
[0044] Example 1 Screening of hereditary breast cancer susceptibility genes in Chinese population
[0045] Materials and methods:
[0046] From June 2011 to July 2012, among patients with breast cancer who were treated in the Cancer Hospital Affiliated to Fudan University, according to the following inclusion criteria, we performed continuous enrollment.
[0047] The inclusion criteria were: age of onset of breast cancer patients ≤35 years old, and at least one blood relative who was also a malignant tumor patient; age of onset of breast cancer >35 years old, but ≤50 years old, and at least two relatives of the same side (paternal lineage) or maternal line) blood relatives are also malignant tumors; breast cancer onset age > 50 years old, and at least 3 blood relatives on the same side (paternal or maternal line) are also malignant tumors.
[0048] The patient's medical history and family history were collected through questionnaires, and 5ml of peripheral blood was collected...
Embodiment 2
[0145] The primers needed for the synthetic kit of embodiment 2
[0146] Primer synthesis: The following primers were designed for the mutation sites described in the present invention, as shown in Table 7. For the primer sequences, please refer to SEQ ID NO: 1 to SEQ ID NO: 152 in the sequence listing.
[0147] Table 7 Tumor mutation site primers
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[0156] The meaning of Ex-Fw and Ex-Rv primers in Table 7 is the first pair of PCR primers in the nested PCR, and the meaning of In-Fw and In-Rv primers is the nested primers in the nested PCR reaction.
[0157] Utilize the primers shown in Table 7 to perform nested PCR on the patient's genomic DNA. The reaction system and reaction program of the nested PCR are conventional techniques in the art, and the nested PCR reaction program can be appropriately adjusted according to the size of the target fragment, and used The resulting PCR produc...
Embodiment 3
[0158] Example 3 Prepare the probes required for the detection kit
[0159] The capture target region of the gene is shown in Table 1: select the exon coding region of the gene to be tested and some flanking intron regions, and use the Agilent Sureselect XT Custom Kit (700Kb-34Mb) (the kit was purchased from Agilent Technologies, Inc. ) to design a probe, the sequence of the obtained probe is the same as or complementary to the gene sequence carrying the pathogenic mutation site shown in Table 4, please refer to the instruction manual of the kit for the design method of the probe.
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