
EnGen Mutation Detection Kit – 25 rxns
RM1,130.00Brand:
New England Biolabs
- Simple protocol for detecting targeting efficiency in genome editing experiments
- Optimized reagents for performing robust T7 Endonuclease-based detection of genome editing events
- Q5® Hot Start High Fidelity 2X Master Mix included for robust amplification, high fidelity and convenience
- Rapid protocol requires no cleanup between PCR and digestion

Gibson Assembly Master Mix
RM880.00 – RM3,305.00Brand:
New England Biolabs
Gibson Assembly allows for successful assembly of multiple DNA fragments, regardless of fragment length or end compatibility.
- Assembly and transformation in just under two hours
- Flexible sequence design (scar-less cloning)
- No PCR clean-up step required
- High transformation efficiencies for inserts up to 20 kb
- Easily adapted for multiple DNA manipulations, including site-directed mutagenesis

NEB PCR Cloning Kit (Without Competent Cells) – 20 rxns
RM920.00Brand:
New England Biolabs
Easy cloning of all PCR products, including blunt and TA ends
- In vitro transcription with both SP6 and T7 promoters
- BsaI-site removed from the ampicillin-resistant gene (allows for the cloning of Golden Gate Assembly modules)
- Fast cloning experiments with 5-minute ligation step
- Simplified screening with low/no colony background and no blue/white selection required

NEBuilder HiFi DNA Assembly Master Mix
RM855.00 – RM3,210.00Brand:
New England Biolabs
NEBuilder® HiFi DNA Assembly Master Mix allows for seamless assembly of multiple DNA fragments, regardless of fragment length or end compatibility. It has utility for the synthetic biology community, as well as those interested in one-step cloning of multiple fragments due to its ease of use, flexibility and simple master-mix format. Visit NEBuilderHifi.com for more information.

Q5 Site-Directed Mutagenesis Kit (Without Competent Cells) – 10 rxns
RM770.00Brand:
New England Biolabs
The Q5® Site-Directed Mutagenesis Kit (Without Competent Cells) enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours.
- Non-overlapping primer design ensures robust, exponential amplification, generating a high percentage of desired mutations from a wide range of templates
- Intramolecular ligation and transformation into NEB high-efficiency competent cells results in high colony yield
- Extremely low error rate of Q5 Hot Start High-Fidelity DNA Polymerase reduces screening time