CRISPR as a Service
A game-changing method for molecular editing, enabling limitless research possibilities.
BACKGROUND
CRISPR/Cas9 technology is the most recent genome editing technique. CRISPR/Cas9 is a simple but potent technology taken from a natural defense mechanism of bacteria and archaea that may be used to target particular locations in the genome. Though only developed in 2013, CRISPR/Cas9 already become a popular genome editing tool, due to its simplicity, versatility, and specificity compared to prior techniques for genome modification.
WHAT WE DO?
At Ankh, we provide a variety of tailored services to fulfil the specific needs of your gene editing projects. Our CRISPR/Cas9 services enable you to speed your genome editing research thanks to their quick turnaround and low cost. For successful genome editing, a specific and potent guide RNA (gRNA) is required. Our custom gRNA cloning service is a low-cost, quick way to further your study. We offer two alternatives for cloning target sequences into any of our CRISPR/Cas9 vectors either you submit the target sequences and a vector, and we build the plasmid for you, or you give a 100-bp genome sequence, and we use our proprietary gRNA design technology to create target sequences for you
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