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Intact Genomics Cas12a Nuclease is the purified recombinant Francisella tularensis Cas12a enzyme for in vitro gene editing. -
Intact Genomics Cas9 Nuclease is the purified recombinant Streptococcus pyogenes Cas9 enzyme containing a nuclear localization signal (NLS). -
FastAmp® Plant Direct PCR Kit is suitable for amplification of DNA directly from plant samples without purifying DNA -
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Intact Genomics FastAmp® Plant Direct RPA kit offers a fast, robust method for amplifying DNA fragments from plant tissues at a single and constant temperature (37°C) using RPA technology. The key highlights of FastAmp® Plant Direct RPA Solution include its simplicity, speed, and reliability. By eliminating the need for DNA extraction, researchers can streamline their workflows, with tissue lysis and genomic DNA ready for RPA in just 3 minutes. -
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FastAmp® qRPA SYBR Kit is a powerful tool to screen primer conditions for the lowest possible Non-template control (NTC) background. Applications and Benefits:- Primer validation and screening.
- Highly selective and sensitive isothermal amplification technique.
- Alternative to PCR. No thermocycler needed.
- Speed and sensitivity.
- No DNA pretreatment required.
- Flexible endpoint detection compatibility (e.g. lateral flow, real-time fluorescence).
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The IG® PE pegRNA synthesis kit is simple to use, and is scalable to help you reach necessary yields of pegRNA -
IG® Recombinase Polymerase Amplification (RPA) Kit provides a mixture of the necessary enzymes to simplify and quicken the setup for your RPA reaction. -
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New improved IG® Recombinase Polymerase Amplification (RPA) Kit v2 provides a mixture of the necessary enzymes to simplify and quicken the setup for your RPA reaction. -
The IG® RNA Cleanup Kit purifies and concentrates up to 50 µg of RNA from enzymatic reactions. -
With high and scalable yield, the IG® sgRNA Synthesis Kit for Cas12a nuclease is the perfect choice for a variety of sgRNA synthesis needs. -
With high and scalable yield, the IG® sgRNA Synthesis Kit for Cas9 nuclease is the perfect choice for a variety of sgRNA synthesis needs. -
(ig®) ccdB Resist™ cells are capable of propagation of plasmids containing the ccdB gene. -
High Efficiency ig® ER2738 Phage Display chemically competent cells are suitable for preparation of antibody or peptide phage display libraries. -
High Efficiency ig® Stable 2 cells are capable of cloning methylated genomic sequences, retroviral sequences and direct repeat sequences. -
High Efficiency ig® XL1 Blue Max chemically competent E. coli cells are suitable for the preparation of high quality plasmid DNA and single strand rescue of phagemid DNA. -
igScript™ Glycerol-free Reverse Transcriptase is a recombinant Moloney Murine Leukemia Virus (MMLV) reverse transcriptase with reduced RNase H activity. It is highly efficient at producing full-length cDNA from long RNA templates. -
JM109 is a K strain that is recA– and endA– to minimize recombination and improve the quality of plasmid DNA. Suitable for high efficiency transformation in a wide variety of applications. -
JM109(DE3) contains a chromosomal copy of the gene for T7 RNA polymerase. -
IG® PEmax enzyme is the purified recombinant Streptococcus pyogenes Cas9 nickase mutant (H840A)-MMLV-Reverse Transcriptase fusion protein containing a NLS. -
Quick10™ Cloning Kit enables assembly to plate in 10 Minutes! -
Staphylococcus aureus RN4220 strain is commonly used in studies involving virulence, resistance, metabolism and more. -
T7 RNA Polymerase is useful for sgRNA and mRNA synthesis, RNA synthesis from DNA templates and applications in mRNA therapeutics. -
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Simplify your large DNA transformation workflow by eliminating time-consuming heat shock, lengthy incubations, and outgrowth procedures. Simply mix and directly plate! -
BL21(DE3)pLysS chemically competent cells allow for tighter control of expression and are suitable for the expression of toxic genes. -
IG® Autoinduction DE3 Chemically Competent Cells are suitable for transformation and routine recombinant protein expressed from a vector under an IPTG-inducible T7 promoter. With simple and less hands-on autoinduction, you can either enjoy more free-time or get more work done. Moreover, the yields of both expressed cells and protein are likely 5-10 fold or more for a broad range of protein targets at either small or large scale of protein production. -
Intact Genomics (IG®) Autoinduction DE3 ElectroCompetent cells are suitable for transformation and routine recombinant protein expressed from a vector under an IPTG-inducible T7 promoter. With simple and less hands-on autoinduction, you can either enjoy more free-time or get more work done. Moreover, the yields of both expressed cells and protein are likely 5-10 fold or more for a broad range of protein targets at either small or large scale of protein production. -
Intact Genomics (IG®) Autoinduction Medium promotes high-yield growth of E. coli and high-level expression of T7 promoter-regulated recombinant proteins without time-consuming steps such as monitoring optical density (OD) or adding induction components like IPTG. Unlike traditional LB-IPTG induction systems, IG® Autoinduction Medium allows regulated protein expression in any expression system that is solely inducible by IPTG from E. coli strains containing a fully functional lac operon. -
(ig®) ccdB Resist™ ElectroCompetent Cells are capable of propagation of plasmids containing the ccdB gene. -
ER2738 Phage Display ElectroCompetent Cells are suitable preparation of antibody or peptide phage display libraries
