Detection kit for relapse and drug resistance gene mutation of acute lymphoblastic leukemia (ALL) and application method thereof
An acute lymphocyte and detection kit technology, applied in the fields of medicine and molecular detection, can solve problems such as affecting clinical prognosis and promoting disease recurrence, achieving the effects of strong applicability, reducing false positives, and accurate detection results
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Embodiment 1
[0045] Composition and preparation of embodiment 1 kit
[0046] In the present invention, for acute lymphoblastic leukemia chemotherapy resistance and relapse-related NT5C2 drug resistance gene, a detection kit and application method for acute lymphoblastic leukemia treatment medication and close detection of relapse are developed. This gene is currently the most promising target for the detection of chemotherapy resistance and relapse of acute lymphoblastic leukemia, and can play an important role in the current and future treatment of acute lymphoblastic leukemia.
[0047] The source of the gene sequence detected by the present invention is the NCBI (National Center for Biotechnology Information) gene bank, and the specific identification and functions are shown in Table 1 below:
[0048] Table 1
[0049]
[0050] The domain distribution diagram of the gene-encoded protein detected by the present invention, such as figure 1 shown.
[0051] The invention provides a kit ...
Embodiment 2
[0061] Example 2 Detection and verification report of the kit
[0062] 1. Name of the test procedure (method) of the acute lymphoblastic leukemia drug detection and recurrence monitoring kit of the present invention: NT5C2 gene mutation detection (PCR-generation sequencing method).
[0063] 2. The purpose of verification: through the analysis and evaluation of the accuracy, sensitivity, and precision of the methodology, the method verification of the testing procedure (methodology) is carried out to meet the needs of clinical experiments.
[0064] 3. Experimental materials:
[0065] 3.1. Specimen type: DNA extracted from peripheral blood.
[0066] 3.2. Reagents: This verification experiment uses the conventional reagents of the molecular platform, and all reagents are within the validity period. The main reagent information is shown in Table 4:
[0067] Table 4 Reagent information used for NT5C2-related gene mutation detection verification
[0068]
[0069] 3.3. Instrume...
Embodiment approach
[0082] The specific implementation is as follows:
[0083] In step S1, peripheral blood is used as the sample to be tested. Genomic DNA can be extracted using a conventional kit column extraction method, and operated according to the instructions of the kit used to collect 50 μL of DNA solution with a concentration of 50-200 ng / μL, which can be directly used Before testing or store at -20°C;
[0084] The verification experiment used 7 specimens, and the specimen type was DNA extracted from peripheral blood. See Table 5 for the specimens.
[0085] Table 5. Specimen information used for NT5C2-related gene mutation detection verification
[0086] sample name
1
DNA extracted from peripheral blood
p16060306
2
DNA extracted from peripheral blood
p16060608
3
DNA extracted from peripheral blood
p16061215
4
DNA extracted from peripheral blood
p16061242
5
DNA extracted from periphe...
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