Invitrogen TrueDesign Genome Editor: Inserting, Replacing or Deleting DNA bases in a gene transcript
5:18
The TrueDesign Genome Editor is a free online tool that enables scientists to easily design, select, and order reagents for precise gene editing.
Related Videos
In Genome Editing Videos
-
Play video Webinar: Expanding the frontiers of gene editing - the role of genotypic confirmation
Webinar: Expanding the frontiers of gene editing - the role of genotypic confirmation
View webinar to learn how genomic confirmation of CRISPR knock-ins, knock-outs and single base changes is critical to successful interpretation of results
1:29:00
-
Play video A step-by-step workflow for a knock-out experiment in an adherent cell line
A step-by-step workflow for a knock-out experiment in an adherent cell line
In this tutorial video, we demonstrate the process of conducting a HPRT gene knock-out experiment in a HEK293 adherent cell line.
11:03
-
Play video SeqScreener Gene Editing Software - Exporting results how-to video
SeqScreener Gene Editing Software - Exporting results how-to video
Check out this video to see how easy it is to export your gene editing data analysis, including figures useful for publications, using the free, user-friendly SeqScreener Gene Edit Confirmation App.
2:29
-
Play video A step-by-step workflow for a knock-out experiment in T cells
A step-by-step workflow for a knock-out experiment in T cells
In this tutorial video, we demonstrate the process of conducting a PDCD1 gene knock-out in T cells.
10:21
-
Play video A step-by-step workflow for a knock-in experiment in an adherent cell line
A step-by-step workflow for a knock-in experiment in an adherent cell line
In this tutorial video, we demonstrate the process of conducting a beta actin gene knock-in in a HEK293 adherent cell line.
9:30
-
Play video CRISPR-Cas9: A transformative tool for treating debilitating genetic disease
CRISPR-Cas9: A transformative tool for treating debilitating genetic disease
Learn how patient-specific iPSC-derived systems are being used to understand the impact of rare genetic mutations on the function of human neuronal subtypes.
4:28
