Thus, these data show that the Cellartis iPSC CRISPR / Cas9 Gesicle and Single - Cell Cloning System effectively edits and expands single - cell
hiPS cell clones without introducing karyotypic abnormalities.
Pluripotency was maintained in edited
hiPS cell clones that were seeded as single cells.
hiPS cell clones that have been edited via gesicles maintain a stable karyotype after editing and clonal expansion.
Graphical representation of indels created at the CD81 target site in different CRISPR / Cas9 - edited
hiPS cell clones.
Not exact matches
This kit utilizes the DEF ‑ CS culture system, recognized for its suitability for genome engineering (Valton et al. 2014) and single -
cell cloning (Feng et al. 2014), to promote reliable growth of
hiPS cells in a feeder - free and defined environment.
Workflow for targeted knockout of CD81, an endogenous gene in
hiPS cells, using the Cellartis iPSC CRISPR / Cas9 Gesicle and Single -
Cell Cloning System.
These data demonstrate that the Cellartis iPSC CRISPR / Cas9 Gesicle and Single -
Cell Cloning System enables highly efficient survival of single
hiPS cells.
To generate your own edited clonal
hiPS cell lines, try one of our complete systems containing a Cas9 - sgRNA RNP complex delivery system (choose electroporation - based or gesicle - based delivery) and the Cellartis iPSC Single - Cell Cloning DEF - CS Culture Media
cell lines, try one of our complete systems containing a Cas9 - sgRNA RNP complex delivery system (choose electroporation - based or gesicle - based delivery) and the Cellartis iPSC Single -
Cell Cloning DEF - CS Culture Media
Cell Cloning DEF - CS Culture Media Kit:
Single -
cell seeding of edited
hiPS cells in this system results in high survival of pluripotent, edited
clones, yielding a diverse set of edited clonal lines.
The Cellartis iPSC CRISPR / Cas9 Gesicle and Single -
Cell Cloning System provides an efficient and effective method to generate clonal lines of edited
hiPS cells.
hiPS cells can be cultured, edited, and clonally expanded using the Cellartis iPSC CRISPR / Cas9 Gesicle and Single -
Cell Cloning System.
CRISPR / Cas9 - mediated editing and single -
cell cloning can be harsh on
hiPS cells.
After gesicle - based delivery of the editing machinery into
hiPS cells,
cells must survive the process of single -
cell cloning — a major bottleneck to obtaining
clones with the modification of interest.
The sequential processes of somatic
cell reprogramming to create patient - specific
hiPS cells, CRISPR / Cas9 gene editing, and single -
cell cloning uniquely enable researchers to study how a specific genetic modification can influence function.