Erythroid Progenitor Isolation

Erythroid progenitor isolation is the process of separating immature red blood cell precursors from bone marrow, peripheral blood, or differentiated stem cell cultures for controlled study. It typically combines tissue dissociation with centrifugation, antibody-based magnetic or fluorescence-activated cell sorting, and selection according to lineage-associated surface markers or cell density. In developmental biology, isolated progenitors allow researchers to examine the progression from hematopoietic stem and progenitor cells through erythroblast maturation, including changes in proliferation, gene expression, and hemoglobin production. This approach supports studies of blood development, anemia, inherited disorders, and the optimization of red blood cell production from stem cells.

Erythroid Progenitor Isolation - Related Videos

Research

JoVE Journal - Developmental Biology

Detection of Residual Donor Erythroid Progenitor Cells after Hematopoietic Stem Cell Transplantation for Patients with Hemoglobinopathies

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Cited by 2 •

2017

Quantification of donor-derived cells is required to monitor engraftment after stem cell transplantation in patients with hemoglobinopathies. A combination of flow cytometry-based cell sorting, colony formation assay, and subsequent analysis of short tandem repeats may be used to assess the proliferation and differentiation of progenitors in the erythroid compartment.

Identification and Analysis of Mouse Erythroid Progenitors using the CD71/TER119 Flow-cytometric Assay

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Cited by 147 •

2011

A flow-cytometric method for identification and molecular analysis of differentiation-stage-specific murine erythroid progenitors and precursors, directly in freshly –harvested mouse bone marrow, spleen or fetal liver. The assay relies on cell-surface markers CD71, Ter119, and cell size.

Direct Lineage Reprogramming of Adult Mouse Fibroblast to Erythroid Progenitors

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Cited by 1 •

2018

Here we present our protocol for producing induced erythroid progenitors (iEPs) from mouse adult fibroblasts using transcription factor-driven direct lineage reprogramming (DLR).

Identification and Isolation of Burst-Forming Unit and Colony-Forming Unit Erythroid Progenitors from Mouse Tissue by Flow Cytometry

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Cited by 13 •

2022

Here, we describe a novel flow cytometric method for prospective isolation of early burst-forming unit erythroid (BFU-e) and colony-forming unit erythroid (CFU-e) progenitors directly from fresh mouse bone marrow and spleen. This protocol, developed based on single-cell transcriptomic data, is the first to isolate all the tissue's erythroid progenitors with high purity.

Isolation of Endothelial Progenitor Cells from Human Umbilical Cord Blood

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Cited by 16 •

2017

The goal of this protocol is to isolate endothelial progenitor cells from umbilical cord blood. Some of the applications include using these cells as a biomarker for identifying patients with cardiovascular risk, treating ischemic diseases, and creating tissue-engineered vascular and heart valve constructs.

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