Kit for prognostic stratification of AML (Acute Myelocytic Leukemia)
A technology of acute myeloid cells and kits, applied in the field of molecular detection, can solve the problems of inability to improve prognosis, poor prognosis, etc., and achieve rapid detection results
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Embodiment 1
[0068] Synthesis of embodiment 1 fluorescently labeled primers
[0069] The following fluorescently labeled primers were synthesized by Shanghai Jierui Company.
[0070]
[0071]
[0072] In the table, F or FS indicates the upstream primer, and R or RS indicates the downstream primer.
Embodiment 2
[0073] Example 2 Detection by PCR and multiple fluorescent capillary gel electrophoresis
[0074] 1) Extraction of total RNA in blood
[0075] a. Take 200 μL of blood, add 1 mL of Trizol (Invitrogen), shake vigorously to mix, and place at room temperature for 10 minutes;
[0076] b. Add 200 μL of chloroform to a, mix vigorously; leave at room temperature for 5 minutes;
[0077] c. 12000rpm, centrifuge at 4°C for 15 minutes;
[0078] d. Aspirate the supernatant into another new 1.5mL centrifuge tube;
[0079] e. Add an equal volume of isopropanol to d and let stand at room temperature for 30 minutes;
[0080] f.12000rpm, centrifuge at 4°C for 15 minutes; discard the supernatant;
[0081] g. Wash the precipitate with 500 μL of 75% ethanol, and wash twice;
[0082] h. with 20μLddH 2 O (no RNase) dissolves the precipitate;
[0083] i. Electrophoresis to detect the integrity of the extracted RNA, and use Qubit or Nanodrop to measure the concentration of RNA.
[0084] 2) Rev...
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