The discovery of CRISPR/Cas9 as a simple and effective tool for targeted modification of cells has opened up new possibilities for gene or cell therapies. Join us to hear about strategies for ...

The CRISPR-Cas9 system provides researchers a powerful tool for manipulation of cells to create disease models, reporter cell lines, cell therapy tools, and approaches for novel pathway discoveries.

Getting CRISPR-Cas9 into primary and stem cells can be tricky. To optimize delivery, says Lonza, try using different transfection methods, CRISPR substrates, plasmids, and means of enriching for ...

CRISPR-Cas9 is a versatile tool to discover more about your biological pathway or gene of interest. The simplicity of the CRISPR-Cas9 system has led to an explosion in applications, from single cell ...

Using CRISPR/Cas9 gene editing technology for the generation of knock-out cell lines and cell lysates ensures the development of useful tools to validate antibody specificity and elucidate gene ...

A new method relying on CRISPR/Cas9 allows the generation of stable cell lines with controlled and physiological levels of transgene expression. A major problem with stable cell lines generated by ...

FinGEEC provides cell line generation and consultation services to researchers from University of Helsinki, Biocenter Finland affiliated universities and other researchers. We provide transgene ...

The replication of potentially harmful adenoviruses can be significantly reduced in human cells in cell culture by using the so-called CRISPR-Cas9 system ("gene scissors"). This method, which is ...

We design and optimize CRISPR/Cas9 single or double guide RNAs for genome editing projects in mammalian cell lines. The service can be requested together with gRNA validation or analytical services ...

AMSBIO has established a comprehensive portfolio of knock-out cell lines and lysates generated with CRISPR/Cas9 technology. Using CRISPR/Cas9 gene editing technology for the generation of knock-out ...