CSR 2X Hot Start Taq Master Mix is a convenient, ready-to-use PCR solution featuring compatibility with a wide range of DNA templates, including mouse, human, plasmid, and bisulfite-converted DNA. It leaves a 3′ adenine overhang, making it ideal for TA cloning. The CSR Hot Start Taq Master Mix offers exceptional value per unit in terms of cost. Hot Start Technology Hot Start Taq DNA Polymerase contains an aptamer based Hot Start technology that prevents amplification during PCR setup and minimizes the amplification of primer-dimer and nonspecific products. Initial incubation at 94 - 95 °C is NOT required. The aptamer contains a 3’ cap that prevents its amplification and ensures no interference with cloning or any downstream analysis.   🍁 Researched, Developed and Manufactured in London, ON, Canada.    Catalogue Number Number of Reactions Volume (mL) M0602-005 50 1.25 M0602-020 200 5.0   Included in the Kit CSR 2X Hot Start Taq Master Mix GC Extender (For GC-rich or difficult to amplify templates) Protocol Specification Robust and reliable reactions Tolerates a wide range of templates Amplification confirmed up to 5 kb in PCR reactions The error rate in PCR is 2.2 x 10^-5 errors per nucleotide per cycle Hot-Start technology prevents the formation of non-specific products in PCR Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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CSR 2X Taq Master Mix is a convenient, ready-to-use PCR solution featuring compatibility with a wide range of DNA templates, including mouse, human, plasmid, and bisulfite-converted DNA. It leaves a 5′ adenine overhang, making it ideal for TA cloning. The CSR Taq Master Mix offers exceptional value per unit in terms of cost.  🍁 Researched, Developed and Manufactured in London, ON, Canada.   Included in the Kit CSR 2X Taq Master Mix GC Extender (For GC-rich or difficult to amplify templates) Protocol  Catalogue Number Number of Reactions Volume (mL) M0501-005 50 1.25 M0501-020 200 5.0   Specification Robust and reliable reactions Tolerates a wide range of templates Amplification confirmed up to 5 kb in PCR reactions Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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CSR High Fidelity DNA Polymerase is a recombinant polymerase that contains a 5’ -> 3’ DNA polymerase and a 3 ‘ -> 5’ exonuclease domains along with a Sso7D tethering domain. The High-Fidelity DNA polymerase achieves 55-fold higher fidelity than Taq DNA polymerase and generates blunt end PCR products. The High-Fidelity DNA polymerase can generate DNA fragments up to 10 Kbp in length with higher accuracy and two-to-three-fold greater processivity than Taq DNA polymerase. Source High Fidelity DNA Polymerase is a recombinant polymerase derived from the archaeon Pyrococcus furiosus. 🍁 Researched, Developed and Manufactured in London, ON, Canada.    Catalogue Number Units Number of Reactions M0401-002 200 U 80 M0401-010 1000 U 400 M0401-050 5000 U 2000   Included in the Kit CSR High Fidelity DNA Polymerase GC Extender (For GC-rich or difficult to amplify templates) 5X High Fidelity PCR Buffer Protocol Specification High fidelity amplification (> 55X Higher than Taq) Robust and reliable amplification Tolerates a wide range of templates 2-3 X faster speeds in PCR reactions (15 - 30 sec/ kb) Resistant to contaminated templates, such as plant DNA Amplification confirmed up to 10 kb in PCR reactions Superior performance for a broad range of templates (High AT to high GC rich) Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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CSR Hot Start Taq DNA Polymerase reliably amplifies a wide variety of DNA templates—including mouse, human, plasmid, and bisulfite-converted DNA—producing consistent PCR products. This polymerase leaves a 3′ adenine overhang, making the products well-suited for TA cloning. Verified extension capabilities reach up to 5,000 base pairs, with speeds of up to 1 kb per minute. Hot Start Technology Hot Start Taq DNA Polymerase contains an aptamer based Hot Start technology that prevents amplification during PCR setup and minimizes the amplification of primer-dimer and nonspecific products. Initial incubation at 94 - 95 °C is NOT required. The aptamer contains a 3’ cap that prevents its amplification and ensures no interference with cloning or any downstream analysis. 🍁 Researched, Developed and Manufactured in London, ON, Canada.  Catalogue Number Units Number of Reactions M0202-010 1000 U 400 M0202-050 5000 U 2000 M0202-500 50,000 U 20,000   Kit Components 10X PCR Buffer 50 mM Magnesium Sulfate GC Extender (For GC-rich templates and difficult templates) Protocol Specifications Generates PCR product with 3'-dA overhangs The error rate in PCR is 2.2 x 10^-5 errors per nucleotide per cycle Generates PCR product of up to 5 kb Aptamer based Hot Start provides a reversible inhibition of non-specific PCR products Stable at room temperature for up to 2 weeks.  Applications Effective in routine and high throughput PCR Incorporates modified nucleotides in PCR. Effective in DNA labeling. Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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CSR Taq DNA Polymerase reliably amplifies a wide variety of DNA templates—including mouse, human, plasmid, and bisulfite-converted DNA—producing consistent PCR products. This Taq polymerase leaves a 5′ adenine overhang, making the products well-suited for TA cloning. Verified extension capabilities reach up to 5,000 base pairs, with speeds of up to 1 kb per minute. 🍁 Researched, Developed and Manufactured in London, ON, Canada.    Catalogue Number Units Number of Reactions M0101-010 1000 U 400 M0101-050 5000 U 2000 M0101-500 50,000 U 20,000   Specifications Generates PCR product with 3'-dA overhangs The error rate in PCR is 2.2 x 10^-5 errors per nucleotide per cycle Generates PCR product of up to 5 kb Stable at room temperature for up to 2 weeks.  Applications Effective in routine and high throughput PCR Incorporates modified nucleotides in PCR.  Effective in DNA labeling.  Kit Components 10X PCR Buffer 50 mM Magnesium Sulfate GC Extender (For GC-rich templates and difficult templates) Protocol Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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CSR dNTP Mix (10 mM ea) is a ready-to-use aqueous solution of dATP, dTTP, dCTP and dGTP at a concentration of 10 mM. The individual bases are at a stock concentration of 100 mM, and then are mixed in RNase/DNase/Protease free water to achieve indicated concentrations. The purity of these bases is > 99 %, as verified by HPLC.   Storage conditions  All components are to be stored at -20 C. These components can be thawed at 4 C prior to use.  Documents SDS Sheet    For Research Use Only. Not for use in diagnostic procedures.

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CSR NaCl (5M) is a Sodium Chloride Solution, prepared using high-purity sodium chloride and ultra-pure water to ensure reliable performance in molecular biology workflows. The solution is sterile-filtered and free of DNase, RNase, and protease contamination, making it ideal for use in sensitive enzymatic and nucleic acid–based applications. 🍁 Researched, Developed and Manufactured in London, ON, Canada. Key Features 5 M NaCl solution (290.33 g/L) Sterile-filtered, enzyme-free (DNase/RNase/Protease-free) Molecular Biology grade Lot-specific Certificate of Analysis (CoA) provided Manufactured in Canada under strict QC standards Applications Preparation of buffers and media Salt gradient preparation in protein and nucleic acid purification Hybridization buffers and nucleic acid precipitation General molecular biology and biochemistry applications Documents Certificate of Assurance (COA) IR000245    For Research Use Only. Not for use in diagnostic procedures.

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CSR TE Buffer (Tris–EDTA) is formulated with 10 mM Tris-HCl (pH 8.0) and 1 mM EDTA to provide a stable environment for nucleic acid storage and handling. The Tris component maintains a constant pH, while EDTA chelates divalent metal ions such as Mg²⁺ and Ca²⁺, protecting DNA and RNA from enzymatic degradation. 🍁 Researched, Developed and Manufactured in London, ON, Canada. Key Features 10 mM Tris-HCl, 1 mM EDTA, pH 8.0 (±0.1) Sterile, DNase-, RNase-, and protease-free Manufactured with high-purity reagents and Type I water Lot-specific Certificate of Analysis (CoA) provided Made in Canada under strict QC standards Applications Long-term storage of DNA and RNA Resuspension of nucleic acid pellets after extraction Preparation of plasmid DNA for cloning, sequencing, or PCR Protection of nucleic acids from nuclease degradation Documents SDS Sheet Certificate of Assurance (COA) IR000244   For Research Use Only. Not for use in diagnostic procedures.

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CSR Ultra-Pure Sterile Water is specially prepared for molecular biology and life science applications requiring the highest purity. It is rigorously purified, autoclaved, and tested to ensure it is completely free of DNases, RNases, and proteases, making it ideal for sensitive workflows where nucleic acid or protein integrity must be preserved. 🍁 Researched, Developed and Manufactured in London, ON, Canada.   Catalogue Number Number of Bottles  Volume MBWTR-500 1 500 mL  MBWTR-P500 10 10 x 500 mL    Key Features Sterile, enzyme-free (DNase/RNase/Protease-free) Endotoxin-tested and prepared with Type I water Certified Molecular Biology grade Lot-specific Certificate of Analysis (CoA) provided Produced in Canada under strict QC standards Applications Preparation of PCR/qPCR master mixes and buffers Dilution or resuspension of nucleic acids and proteins Preparation of enzyme reactions requiring nuclease-free conditions General molecular biology workflows requiring ultra-pure water Documents SDS Sheet Certificate of Assurance (COA) IR000241   For Research Use Only. Not for use in diagnostic procedures.

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CSR Tris Buffer, (pH 10.0 or pH 8.0 available), is manufactured to the highest molecular biology standards, ensuring consistency and reliability in sensitive applications. This 1 M solution, adjusted to pH 8.0 or 10.0, is sterile-filtered and certified free of DNase, RNase, and protease contamination. Designed for use in a wide range of molecular biology workflows, it provides a stable buffering environment that supports nucleic acid integrity and enzymatic activity. 🍁 Researched, Developed and Manufactured in London, ON, Canada. Catalogue Number Number of Bottles  pH Volume MBTRIS-P8 1 8.0 500 mL  MBTRIS-P10 1 10.0 500 mL    Key Features 1 M Tris-HCl buffer Sterile, endotoxin-free, and enzyme-free (DNase, RNase, protease) Prepared with ultra-pure reagents and Type I water Lot-specific Certificate of Analysis (CoA) provided Manufactured in Canada under strict QC standards Applications PCR/qPCR and RT-PCR reactions Preparation of electrophoresis buffers (TAE, TBE) RNA and DNA resuspension or dilution Enzyme reactions requiring nuclease/protease-free conditions General molecular biology and biochemistry workflows Key Documents SDS Sheet Certificate of Assurance (COA) IR000243   For Research Use Only. Not for use in diagnostic procedures.

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CSR MycoZap is a Mycoplasma prevention spray that provides a fast, reliable, and convenient solution for maintaining contamination-free cell culture environments. Unlike traditional cleaning methods—such as wiping with sponges or paper towels, which risk spreading microbes from one surface to another—MycoZap acts directly at the source. Its powerful formulation targets and eliminates a broad spectrum of laboratory contaminants, including mycoplasma, bacteria, and viruses, helping to safeguard your valuable experiments. 🍁 Researched, Developed and Manufactured in London, ON, Canada. Features Eradicates mycoplasma Non-corrosive an non-carcinogenic Convenient and stable Ready-to-use Instructions for Use Spray the Mycoplasma prevention solution directly onto the desired surface, ensuring even coverage Allow the solution to sit for 10 minutes to maximize its effectiveness Wipe the surface dry using a clean paper towel or disposable cloth. What are mycoplasma? Mycoplasma are especially troublesome because they lack a cell wall and evade many antibiotic treatments. Once inside cell culture samples, they can silently compromise experimental data. The best strategy is prevention—and that’s where MycoZap excels. Designed for routine use in incubators, hoods, benchtops, storage containers, and instruments, MycoZap offers comprehensive protection against unwanted microbial invaders. Using MycoZap is simple: spray directly onto surfaces and equipment, allow 10 minutes for action, and the treated area is effectively decontaminated. This ready-to-use solution is non-corrosive, non-carcinogenic, and formulated for everyday laboratory workflows. Regular use of MycoZap significantly reduces the risk of contamination events, protecting both your cells and your research. With MycoZap, labs can achieve peace of mind knowing their culture areas remain free of hidden threats—quickly, easily, and cost-effectively. Documents SDS Sheet    For Research Use Only. Not for use in diagnostic procedures.

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CSR ROBUST DNA Polymerase is a highly efficient next-generation DNA polymerase offering enhanced processivity and yield compared to Taq DNA polymerase. This enzyme enables shorter extension times and fewer cycles to achieve equivalent levels of amplification. It also features significantly improved resistance to various PCR inhibitors, chemical denaturants, and increased thermal stability, maintaining activity even after 1 hour at 95 °C. Its enhanced robustness allows for the use of lower-quality template DNA and simplifies DNA purification protocols. The ROBUST DNA Polymerase utilizes aptamer-based hot start technology, providing reversible inhibition that prevents primer-dimer formation and non-specific amplification, enabling reaction setup at room temperature. Hot-Start Technology The CSR ROBUST DNA Polymerase contains an aptamer based Hot Start technology that prevents amplification during PCR setup and minimizes the amplification of primer-dimer and nonspecific products. Initial incubation at 94 - 95 °C is NOT required. The aptamer contains a 3’ cap that prevents its amplification and ensures no interference with cloning or any downstream analysis. 🍁 Researched, Developed and Manufactured in London, ON, Canada. Included in the Kit CSR ROBUST DNA Polymerase 50 mM Magnesium Sulfate GC Extender (For GC-rich or difficult to amplify templates) Protocol  Catalogue Number Units Number of Reactions M0301-002 200 U 80 M0301-010 1000 U 400 M0301-050 5000 U 2000   Specification Robust and reliable reactions Compatible with contaminated templates, such as plant DNA. Compatible with direct colony PCR.  2-3 X faster speeds in PCR reactions (15 - 30 sec/ kb) Tolerates a wide range of templates Amplification confirmed up to 5 kb in PCR reactions The error rate in PCR is 2.2 x 10^-5 errors per nucleotide per cycle Hot Start technology prevents the formation of non-specific products in PCR Stable at room temperature for up to 2 weeks.  Documents Product Information Sheet Quick Guide Sheet SDS Sheet For Research Use Only. Not for use in diagnostic procedures.

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