CRISPR cell service now available !
We are pleased to announce we have recently added CRISPR/Cas9 gene-editing in cells to the list of services we offer.
CRISPR technology enables the production of a number of mutations not previously possible using conventional gene targeting. We can generate knock-out, knock-in, point-mutated and tagged versions of your favourite gene in a wide variety of both human and mouse cell lines.
We offer a full service, from project design to delivery of modified clones and supported by NCRIS funding, this service is available to researchers at a heavily subsidised price.
Use one of our proven cell lines: hESC; HEK293; MDA-MB-231; A549; MCF7; KPC; C26; mESC; or suggest your own to use, we are happy to discuss the possibilities.
Supported by NCRIS funding, this service is available to researchers at a heavily subsidised price.