L-type PML/RAR alpha fusion gene detection kit and corresponding detection method

A detection kit and fusion gene technology, applied in the field of blood molecular biology, can solve the problems of cumbersome operation, high detection cost, and low specificity, and achieve the effects of early recurrence, recurrence prediction, and simple operation

Inactive Publication Date: 2014-08-27
SHANXI MEDICAL UNIV
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Problems solved by technology

[0003] At present, the detection methods of PML / RARα fusion gene mainly include chromosome analysis, real-time quantitative RT-PCR, fluorescence in situ hybridization, etc., but these methods have problems such as low specificity, cumbersome operation, and high detection cost, which limit their wide application. [Wei Na, Chen Jinghua, Wang Kun, et al. Research on the Electrochemical Sensor of Hairpin Structure DNA Probes for Detection of Leukemia PML / RARα Fusion Gene[J]. Journal of Analysis and Testing, 2008, 27(9): 907-910]

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  • L-type PML/RAR alpha fusion gene detection kit and corresponding detection method
  • L-type PML/RAR alpha fusion gene detection kit and corresponding detection method
  • L-type PML/RAR alpha fusion gene detection kit and corresponding detection method

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Embodiment Construction

[0023] The present invention will be further described below in conjunction with embodiments, but the present invention is not limited to the content of the embodiments.

[0024] An L-type PML / RARα fusion gene detection kit, consisting of the following components: functionalized graphene oxide, FITC-labeled single-stranded DNA with the sequence 5'FITC-TGACCTGCCATTGAG-3', reagent I, formaldehyde, saponin , PBS buffer, the concentration and dosage of each component in the kit are shown in Table 1. The amount of reagent listed is 10 sample reactions:

[0025] Table 1

[0026] Serial number Reagent name Volume ml Explain 1 Functionalized Graphene Oxide0.2 Concentration 2 mg / ml 25 , FITC-TGACCTGCCATTGAG-3 , 2The concentration is 1μmol / l; the purity is HPLC grade; 5 , The end 7 bases are located in the PML gene, 3 , The end 8 bases are located in the RARa gene 3 Reagent Ⅰ7.8 4 formaldehyde1.0 Concentration 10%V / V 5 Saponin1.0 Concentration 0.05%V / V 6 PBS buffer130 Concentration 0.1mo...

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Abstract

The invention relates to the blood molecular biology field, and concretely relates to an L-type PML / RAR alpha fusion gene detection kit and a corresponding detection method. The L-type PML / RAR alpha fusion gene detection kit is composed of the following reagents of a functional oxidized grapheme, FITC-labeled single chain DNA with a sequence of 5'-FITC-TGACCTGCCATTGAG-3', a reagent I, formaldehyde, Escin and a PBS buffer, wherein the reagent I is composed of Tris alkali, NaCl, KCl, MgC12, HCl and H2O, an application method comprises the steps of cells culture, incubation liquid preparation by co-incubation with cells, and cells pretreatment and co-incubation of an incubation liquid and cells. The reagent provided by the kit can rapidly and accurately detect that whether certain cell exists the L-type PML / RAR alpha fusion gene or not, the kit has the advantages of sensibility, specificity, simple operation and rapidity, and the kit has important meaning for APL diagnosis and minimal residue monitoring, and the kit can realize recurrence prediction at early stage and clinical treatment guidance.

Description

Technical field [0001] The invention belongs to the field of blood molecular biology, and specifically relates to an L-type PML / RARα fusion gene detection kit and a corresponding detection method. Background technique [0002] Leukemia is a type of clonal malignant disease with abnormal hematopoietic stem cells. The leukemia cells in the clone lose the ability to further differentiate and mature and are stagnated at different stages of cell development. In the bone marrow and other hematopoietic tissues, leukemia cells proliferate and accumulate in large numbers and infiltrate other organs and tissues, while suppressing normal hematopoiesis. The clinical manifestations are symptoms of anemia, bleeding, infection and infiltration of various organs. Chromosomal abnormalities are one of the common causes of leukemia. According to the maturity of leukemia cells and the natural course of the disease, leukemia can be divided into acute and chronic categories. The differentiation of ...

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/68
Inventor 李然王宏伟覃艳红陈秀花任方刚张耀方徐智芳李莉郭海秀王晓娟
Owner SHANXI MEDICAL UNIV
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