Unleash the full power of a well-designed library. With Twist Bioscience, you are assured that the library you design contains the specific modifications, exactly where you want them, saving you valuable resources for the downstream screening process.
500 x 20 µl reactions, 5 ml (5 x 1 ml) 2x one-step reaction mix containing iTaq DNA polymerase, buffers, and ROX normalization dyes; iScript™ reverse transcriptase; and nuclease-free water
100/120 V, handheld biolistic system, includes gene gun, 5 O-rings, 5 barrel liners, 5 white cartridge holders, cartridge extractor tool, 9 V battery Â
100/120 V, handheld biolistic system, includes helium hose assembly with low-pressure regulator, tubing prep station (#165-2418), syringe kit, tubing cutter, optimization kit (#165-2424) Â
BioReagent, for molecular biology, ≥99%5
Genetic engineering is the process of manipulating the genetic material of an organism — often to include the DNA from a foreign organism. Using the classic pGLO Bacterial Transformation Kit, students transform bacteria by introducing a gene from the bioluminescent jellyfish Aequorea victoria. The same procedure has been used to create "designer proteins" which have led to the explosion of new health treatments, agricultural a…
mMESSAGE mMACHINE® kits are designed for the in vitro synthesis of large amounts of capped RNA. Capped RNA mimics most eukaryotic mRNAs found in vivo, because it has a 7-methyl guanosine cap structure at the 5' end. mMESSAGE mMACHINE® kit reactions include cap analog [m7G(5')ppp(5')G] in an ultra high-yield transcription reaction. The cap analog is incorporated only as the first or 5' terminal G of the transcript because its s…
Ideal for identifying potential therapeutic targets involved in the development and progression of disease
Ideal for whole genome surveys to identify novel targets in biological pathways and disease development
SHERLOCK is an evolution of CRISPR technology, which others use to make precise edits in genetic code. SHERLOCK can detect the unique genetic fingerprints of virtually any DNA or RNA sequence in any organism or pathogen. Developed by our founders and licensed exclusively from the Broad Institute, SHERLOCK is a method for single molecule detection of nucleic acid targets and stands for Specific High Sensitivity Enzymatic Report…
Recombinantly produced in E. coli, CUTANA™ pAG-MNase for ChIC/CUT&RUN Workflows is a fusion of Proteins A and G to Micrococcal Nuclease. This construct is useful in performing Chromatin Immunocleavage (ChIC) and Cleavage Under Targets and Release Using Nuclease (CUT&RUN). CUTANA™ pAG-MNase contains a C-terminal 6xHis epitope tag. CUTANA™ pAG-MNase for ChIC/CUT&RUN Workflows Formulation: CUTANA™ pAG-MNase is provided as a 20…
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
The BioXp™ system is the world’s first and only synthetic biology workstation for building libraries, gene fragments, clones, and more.
Gibson Assembly ® RapidAMPâ„¢ Ultra kit provides a single day, seamless, assembly-to-transfection-ready DNA workflow.Â
Gibson Assembly Ultra kit builds on Codex DNA’s original Gibson Assembly ® technology to expand the ranges of fragment size, fragment number, and project complexity that are compatible with scarless and high-fidelity cloning.Â
The Gibson Assembly ®  HiFi kit uses the original Gibson Assembly ®  cloning* method, which has been optimized for the seamless joining of up to five inserts into a plasmid vector, resulting in DNA constructs with reliably low error rates.
Synthetic single guide RNAs for efficient gene knockout & unparalleled specificity
Synthetic guide RNAs for efficient gene knockout & unparalleled specificity
Single guide RNA expressing vectors for effective and accurate gene knockout
Combine sgRNA and Cas9 nuclease expression into a single vector for simplified delivery
Our CRISPR Design Tool enables an intuitive one-stop location for guide RNA design and ordering. Utilize the design tool to order guide RNAs for targeted gene knockout or location-specific HDR-mediated genome editing.
Optimize your CRISPR-Cas9 experiments with our specific controls and primers
A direct and efficient set of tools to study a gene’s function by overexpression in its native context
For seamless DNA cloning in a lyophilized format
