Method for establishing PDX model of chronic myeloid leukemia
A chronic granulocyte and establishment method technology, applied in the field of PDX model establishment, can solve the problems of lack of effective treatment methods and achieve good application prospects
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[0052] 1. Sample processing of CML patients:
[0053] 1. Collect 10-25 mL of bone marrow from the patient, centrifuge with Ficoll separation medium, and separate mononuclear cells from the patient. After washing the mononuclear cells twice with normal saline, resuspend in 0.5 mL of normal saline, and count the cells.
[0054] 2. For patients with blast phase, CD34 + Sorting: (2) Add rabbit anti-human CD34 antibody to the cells in step (1), incubate on ice for 20 minutes, wash excess antibody with PBS, resuspend in 0.5mL PBS, and sort out CD34 by flow cytometry + Hematopoietic stem / progenitor cells; the sorted cells were counted, resuspended in 0.2-1mL PBS, and injected into mice through the tail vein, and the number of inoculated cells was 1×10 6 / Only.
[0055] 2. Feeding and inoculation of NSG mice:
[0056] 1. Raising conditions for mice: 8-week-old female NSG mice were raised under SPF grade conditions. The room temperature is 18-25°C, the relative humidity is 40%-60%,...
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