• crb's Kodaq DNA Polymerase is the solution for a robust PCR system with high fidelity and yield. crb’s Kodaq DNA Polymerase is a novel DNA polymerase with strategically engineered mutations resulting in a robust, high fidelity polymerase. Kodaq DNA polymerase has exceptional 3’ to 5’ exonuclease activity that endows it with superior accuracy over competitor polymerases. This novel enzyme has intrinsically high processivity and is engineered to have an improved binding affinity for DNA resulting in highly successful PCR. The Kodaq DNA Polymerase advanced and sophisticated buffer system not only tolerates high AT and GC content, but also many PCR inhibitors commonly found in a typical DNA sample. Benefits of crb's Kodaq DNA Polymerase
    • High fidelity PCR
    • Robust PCR performance, resistant to most PCR inhibitors commonly found in samples (including plant samples)
    • PCR success with A/T and G/C rich templates
    • Highly processive, for high yield amplification
      Quantity: 250 U (50 μl)
         
  • Streamline your PCR with crb’s, crb 2X PCR MasterMix crb’s, crb 2X PCR MasterMix provides all ingredients necessary for PCR in a premixed and optimized format that simplifies the PCR workflow. This strategically-engineered polymerase has exceptional sensitivity and can amplify even the most difficult templates (compared to the leading competitors). In addition, crb 2X PCR MasterMix has high fidelity and ultra-low error rates (over 1,000X less than Taq polymerase, representing the lowest error rate on the market), making it incredibly useful for a variety of PCR applications demanding high fidelity, including Next Generation Sequencing, molecular cloning, or diagnostics.   Unit Quantity: 400 rxn (4 x 1.25 ml)
     
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    crb DNA Polymerase offers incredible sensitivity and speed, even with challenging templates, including GC-/AT-rich and long amplicons crb DNA polymerase sets new standards for sensitive, robust, and high-fidelity PCR performance.  This strategically-engineered polymerase has exceptional sensitivity and can amplify even the most difficult templates (compared to the leading competitors). In addition, crb DNA Polymerase has high fidelity and ultra-low error rates (over 1,000X less than Taq polymerase, representing the lowest error rate on the market), making it incredibly useful for a variety of PCR applications, including Next Generation Sequencing, molecular cloning, or for diagnostics.   Unit Quantity: 400 rxn (200 µl)
       
  • Accuracy. Versatility. Convenience.

    The crb®Cycler 96 System is a high-performance, medium- to high-throughput PCR platform (96-well plates) that provides various methods for gene detection, gene expression analysis, genetic variation analysis, and array data validation. The system features the crb®Cycler 96 Instrument, a versatile, plate-based real-time PCR device that supports mono- or multicolor applications as well as multiplex protocols. The benchtop instrument is easily customizable to meet changing user requirements, and can be integrated into everyday use as a robotically controlled, automated high-throughput solution.
     
     
       
  • Innovative. Intuitive. Accurate. Dependable.

    For today's labs, the new crb®Cycler 48 System is the optimal mid-size, mid-throughput real-time PCR solution that conveniently delivers the highest standards expected from a crb®Cycler System: An ideal combination of accuracy, temperature homogeneity, and reproducibility, matched with powerful software so intuitive that it is accessible to any user. The crb®Cycler Instrument is a real-time PCR instrument for rapid cycling up to 48 samples. Applications include absolute and relative quantification, melting curve analysis, and endpoint genotyping. Precise crb®Cycler 48 Instrument thermal homogeneity and cycling speed produce accurate and reproducible results in a very short time. The crb®Cycler 48 Instrument’s optical detection system flexibly detects sequence-dependent probes (i.e., hydrolysis probes) and sequence-independent dyes (i.e., SYBR Green I). Multiplex and multicolor capabilities permit the use of up to four different fluorescent dyes*. The innovative crb®Cycler 48 Application and Instrument Software creates a simple analysis workflow with easy import and export functions, email notifications after each run, online monitoring flexibility, and server-based network interfacing.
     
         
  • Streamline your NGS Library Preparation with crb’s DNA Library Prep kit for Illumina. Our kit contains all reagents needed to convert 2ng – 500ng of DNA fragments into fully compatible Illumina libraries. It allows researchers to get from fragmented DNA to Illumina compatible libraries in as little as two hours. Unit: 48 Reactions
  • Streamline your NGS Library Preparation with crb’s DNA Library Prep kit for Illumina Our kit contains all reagents needed to convert 2ng – 500ng of DNA fragments into fully compatible Illumina libraries. It allows researchers to get from fragmented DNA to Illumina compatible libraries in as little as two hours.   Unit: 12 Reactions
       
  • Cloning Optimizer consists of a proprietary enzyme that can completely eliminate background colonies when cloning Treatment of PCR amplified DNA with this innovative optimizer will remove the trace amounts of plasmid template DNA that remain after PCR. Cloning Optimizer eliminates non-linearized template plasmids that cause false-positive colonies.   Quantity: 200 μl
     
  • The Ligation-Free Cloning kit is a versatile system to meet the demands of routine cloning projects The progressive design has eliminated the requirement for compatible ends and unique restriction sites within the vector and inserts to be cloned. At the foundation of Ligation-Free Cloning technology is crb’s proprietary Ligation-Free Enzyme Mix which reliably facilitates the assembly of up to 3 DNA inserts (PCR-generated sequences) and a linearized vector by recognizing a 15 bp overlap region at both ends. This 15 bp overlap can be engineered by designing primers for amplification of your desired sequences to create inserts free from any redundant or unwanted base pairs. To eliminate the possibility of mutations associated with PCR amplification, scientists at crb have developed a DNA Polymerase with the highest proof-reading capability thus making this system the most reliable on the market.   Quantity: 100 Reactions
       
  • The In vitro DNA Amplification Kit now provides end users with a faster and more efficient technique for high yield DNA amplification from minimal starting template With a simple set up and short handling time, this has now become the method of choice for any application requiring high throughput DNA amplification. The hassle-free protocol eliminates the requirement for mini prep DNA isolation, thus significantly reducing the cost and time required to obtain your amplified product from the reaction. Applications of this technology include (but are not limited to) whole genome amplification, DNA library construction, SNP genotyping and in vitro cloning of lethal DNA.   Quantity: 100 Reactions
       
  • OneScribe T7 Transcription kit is a complete reagent kit designed for in vitro transcription of RNA utilizing T7 RNA Polymerase This kit can synthesize RNA transcripts in high yield including unlabelled, labelled, specific activity RNA, or capped RNA suitable for variety of application such as in vitro translation, antisense studies, and RNA-binding protein studies.   Quantity: 50 Reactions
     
  • The Pro Ligation-Free Cloning Kit allows for the robust assembly of multiple DNA fragments in one step Using a ligation-independent cloning method, as many as six DNA fragments are assembled seamlessly without concern for restriction enzyme site availability. crb’s Pro Ligation-Free cloning is a simple yet highly versatile method to rapidly clone highly complex, multiple component constructs.   Quantity: 20 Reactions