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
|
-
-
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) -
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) -
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 -
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 -
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: 50 Reactions -
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. Qunatity: 25 Reactions -
dNTP Set consists of 100mM aqueous solutions of dATP, dCTP, dGTP and dTTP each supplied in a separate vial Since the nucleotides are provided separately, the dNTP Set offers maximum flexibility in preparation of reaction mixes for different applications. Quantity: 250 µl, 10 mM each
