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$185.00–$700.00Price range: $185.00 through $700.00
igScript™ One Step RT-PCR kit combines two powerful mixtures: i) igScript™ Reverse Transcriptase and ii) Hot start Taq 2x master mix providing improved PCR efficiency, wider dynamic range, superior sensitivity and specificity. The two mixtures require minimal handling during reaction setup and offer consistent and robust RT-PCR reactions.
igScript™ Reverse Transcriptase is a recombinant MMLV reverse transcriptase with reduced RNase H activity and increased thermostability. The kit is highly efficient at producing full-length cDNA from long RNA templates at temperatures between 42-55ºC.
Hot start Taq 2x master mix is a ready-to-use cocktail containing all components except primers and template, for the amplification and detection of DNA in PCR. The hot start Taq 2x master mix contains standard buffer, chemically modified hot start Taq polymerase, MgCl2, dNTPs and stabilizers. The amplification step features a high-quality hot start Taq DNA Polymerase which offers higher fidelity and better amplification.
Applications
Gene expression data validation.
Multiplexing
Mutation detection
Pathogen and viral detection
Genetically modified organisms (GMO) characterization and Genetic profiling
Benefits
Enhanced efficiency, specificity, and sensitivity
Compatible with all real-time PCR instruments
Superior gene expression results under various cycling conditions
Robust and active for cDNA synthesis at temperatures up to 55°C.
igScript™ One Step RT-PCR Kit Includes
ig Script™ Reverse Transcriptase
Hot start Taq 2x Master Mix
Storage Temperature –20 °C
Technical Support & Customer Services
Intact Genomics (IG®) is dedicated to customer satisfaction regarding the use of our products for your research
needs. Each new lot of our products is thoroughly tested to ensure it meets high quality standards and provides
excellent results. We appreciate your business and your feedback regarding the performance of our products in
your applications.
Mix and then centrifuge briefly to collect contents at the bottom of the tube.
Prepare a master mix for each reaction and control requiring Reverse Transcriptase enzyme plus 10% extra to allow for pipetting error according to the following table:
Prepare a master mix for each control requiring NO Reverse Transcriptase enzyme plus 10% extra to allow for pipetting error according to the following table:
Mix the reaction mixture thoroughly.
Program the thermal cycler according to the manufacturer’s instructions.
A typical PCR cycling program is outlined in the following table.
Place the PCR tubes in the thermal cycler and start the cycling program.
Analyze 5-10 μl of PCR products by agarose gel electrophoresis.
