We obtained primary cells from two recently diagnosed AML patients (referred to as PT1 and PT2) who had high leukocyte counts via leukapheresis. To enrich mononuclear cells, we used Ficoll and then lysed them with a red blood cell lysis buffer from Biosharp, China. We subsequently cultured the primary AML cells in RPMI 1640 containing 10% FBS to use in different experiments.
Isolation and Culture of Primary AML Cells
We obtained primary cells from two recently diagnosed AML patients (referred to as PT1 and PT2) who had high leukocyte counts via leukapheresis. To enrich mononuclear cells, we used Ficoll and then lysed them with a red blood cell lysis buffer from Biosharp, China. We subsequently cultured the primary AML cells in RPMI 1640 containing 10% FBS to use in different experiments.
Variable analysis
- Newly diagnosed AML patients
- Healthy controls
- Mononuclear cells isolated from bone marrow samples
- Primary AML cells obtained via leukapheresis
- Bone marrow samples collected between 4 March 2016 and 30 January 2022 at Zhongda Hospital (affiliated with the Southeast University)
- Written informed consent from all enrolled patients collected according to the tenets of the Helsinki Declaration
- Study approved by the Ethics Committee (Zhongda Hospital, Southeast University)
- Primary AML cells from two recently diagnosed AML patients (PT1 and PT2) with high leukocyte counts
- Healthy controls
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