CRISPR-Cas9 Editing of Hematopoietic Stem and Progenitor Cells
In this webinar, Dr. Mark DeWitt, Postdoctoral Fellow at University of California, discuss the use of gene editing techniques for hematopoietic stem and progenitor cells (HSPCs).
Related Multimedia
-
New Tools for the Ex Vivo Expansion of Human Hematopoietic Stem and Progenitor Cells
Publish Date: March 09, 2015 Views: 634 -
Targeting Self-Renewal Function in Normal Hematopoietic and Leukemic Stem Cells
Publish Date: February 03, 2017 Views: 287 -
Using CRISPR/Cas9 to Model Stem Cell Organization and Dynamics
Publish Date: August 25, 2017 Views: 488
Explore Our Products
-
Cas9 nuclease for the generation of double-strand breaks in CRISPR-Cas9 genome editing
-
Enhanced green fluorescent protein (eGFP)-tagged Cas9 nuclease for the generation of double-strand breaks in CRISPR-Cas9 genome editing
-
Custom-designed CRISPR RNA for guide RNA generation in CRISPR-Cas9 genome editing
-
ArciTect™ Human HPRT Positive Control Kit
Positive control for CRISPR-Cas9 genome editing