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Unlock new insights in blood cell research with iCell® Hematopoietic Progenitor Cells 2.0, derived from human induced pluripotent stem cells (iPSCs).
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iCell Hematopoietic Progenitor Cells 2.0 Kit, 01279
iCell® Hematopoietic Progenitor Cells 2.0 are highly pure multipotent progenitor cells with the ability to differentiate into blood cell lineages. These cells can be consistently generated from human induced pluripotent stem cells in large-scale quantities, thereby overcoming the high variability and limited quantities associated with primary CD34+ cord blood or peripheral blood cells.
Our specialists are here to help you find the best product for your application.
Our regular business hours are 9:00am to 5:00pm Central Time (USA)
Our specialists are here to help you find the best product for your application.
Our regular business hours are 9:00am to 5:00pm Central Time (USA)
iCell Hematopoietic Progenitor Cells 2.0 display typical morphology as freely floating round cells.
Figure 1: Morphology of iCell Hematopoietic Progenitor Cells 2.0
Figure 2: iCell Hematopoietic Progenitor Cells 2.0 Reproducibly Express Hematopoietic Progenitor Cell Markers
(A, B) Cells analyzed by flow cytometry at thaw are >90%+ for hematopoietic cell surface markers. (C) Percentage of cells expressing hematopoietic cell surface markers after thaw. Data shown as mean ±SEM; n=13.
iCell Hematopoietic Progenitor Cells 2.0 were plated in colony-forming unit (CFU) assays using a methylcellulose-based medium. (A) Representative images of colonies are shown. (B) CFU frequencies are shown, including erythroid (BFU-E), granulocyte/macrophage (CFU-M, CFU-G, CFU-GM) and mixed colonies (CFU-GEMM). Data shown as mean ±SEM; n=13.
Figure 3: iCell Hematopoietic Progenitor Cells 2.0 Reproducibly Generate Colonies of Multiple Lineages
iPSC-Derived Human Microglia-like Cells to Study Neurological Diseases Abud EM, Ramirez RN, Martinez ES, Healy LM, Nguyen CHH, Newman SA, Yeromin AV, Scarfone VM, Marsh SE, Fimbres C, Caraway CA, Fote GM, Madany AM, Agrawal A, Kayed R, Gylys KH, Cahalan MD, Cummings BJ, Antel JP, Mortazavi A, Carson MJ, Poon WW, Blurton-Jones M (2017) Neuron. 94(2):278-293 (2017)