HiScript III All-in-one RT SuperMix Perfect for qPCR is an upgraded version of HiScript III RT SuperMix for qPCR(+gDNA wiper). Genomic DNA elimination and reverse transcription can be simultaneously completed, which is convenient. It can greatly reduce contamination and RNA degradation. This kit contains HiScript III Reverse Transcriptase, heat-labile DNase and an optimized buffer system. Among them, heat-labile DNase takes effect quickly. It has high efficiency, and can be easily inactivated. The obtained cDNA can be stored stably for a long time. It is compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.

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HiScript II Reverse Transcriptase, optimized from M-MLV (RNase H-) Reverse Transcriptase, is a new generation reverse transcriptase with highly improved thermo stability and cDNA synthesis efficiency. The HiScript II Q RT SuperMix for qPCR (+gDNA wiper) is specially designed for 2-step qRT-PCR. The residual genomic DNA in RNA template can be removed rapidly and completely with the 4 × gDNA Wiper Mix. The 5 × HiScript qRT SuperMix II contains all necessary components required for reverse transcription. With the addition of template RNA and ddH2O, the reaction can proceed quickly. Meanwhile, gDNA wiper is terminated to ensure the integrity of the cDNA. This product has been specially optimized for qPCR. With the optimized proportion of Random primers/Oligo (dT)23VN primer mix, cDNA synthesis can start from each region of RNA transcript and have the same reverse transcription efficiency, which ensures the authenticity and reproducibility of qPCR results to the greatest extent. The cDNA products are compatible with SYBR Green and probe qPCR, and can be used with the corresponding reagent according to the experimental purpose to perform high-performance gene expression analysis.

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The Vazyme HiScript II Reverse Transcriptase, optimized from M-MLV (RNase H-) Reverse Transcriptase, is a new generation reverse transcriptase with highly improved heat stability and cDNA synthesis efficiency. The HiScript II Q Select RT SuperMix for qPCR is designed for 2-step RT-qPCR. The 5× HiScript II Select qRT SuperMix contains Buffer, dNTPs, HiScript II Reverse Transcriptase, and RNase inhibitor. The Oligo (dT)23VN has a better affinity to Ploy A+ RNA than Oligo (dT)18. In addition, random hexamers and gene-specific primers (GSP) are also optional.. The HiScript II Q Select RT SuperMix for qPCR has been specially optimized for qPCR. The cDNA products are compatible for SYBR- or probe-basded qPCR, such as AceQ qPCR SYBR Green Master Mix (Vazyme, #Q111), ChamQ SYBR qPCR Master Mix (Vazyme, #Q311), ChamQ Color SYBR qPCR Master Mix (Vazyme, #Q411), and AceQ qPCR Probe Master Mix (Vazyme, #Q112).

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This product is based on the cost-effective HiScript ® II Reverse Transcriptase and uses uniquely designed Oligo(dT) 23 VN primers to improve the specificity and sensitivity of the reaction and obtain better quality cDNA. Different types of reverse transcription primers can be used flexibly for different experimental designs to meet diverse experimental needs. Oligo (dT) 23 VN primer/Random Hexamers or gene-specific primers (GSP) can be selected according to the needs of subsequent reverse transcription experiments. At the same time, the reaction system is greatly simplified. 5 × qRT SuperMix contains all the reagents required for reverse transcription reaction except the primers and will not freeze at -20°C, making it easy to use. The 4 × gDNA wiper Mix in the kit can completely remove residual genomic DNA contamination, ensuring that the subsequent quantitative results are more reliable. The product obtained by reverse transcription can be used in SYBR ® Green qPCR analysis method and probe analysis method for high-performance gene expression analysis.

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HiScript® II Reverse Transcriptase is a new reverse transcriptase obtained through in vitro molecular evolution technology based on M-MLV (RNase H-) Reverse Transcriptase, which greatly improves thermal stability and cDNA synthesis efficiency. HiScript® II Q RT SuperMix for qPCR is suitable for two-step qRT-PCR detection. 5 × HiScript II qRT SuperMix contains all the components required for reverse transcription reaction. The reaction can be performed quickly by adding template RNA and water. The volume of RNA template can be added up to the total volume It is very suitable for the reverse transcription reaction of low-concentration RNA template. 5 × HiScript® II qRT SuperMix will not freeze at -20°C and is easy to use.
This product is specially optimized for qPCR. Oligo (dT)23VN has stronger anchoring ability to Poly A+ mRNA than Oligo (dT)18, making reverse transcription more efficient. The optimized ratio of Random primers/Oligo (dT)23VN primer mix enables cDNA synthesis to start from each region of the RNA transcript and has the same reverse transcription efficiency, ensuring the authenticity and repeatability of qPCR results to the greatest extent. The reverse transcription product is compatible with SYBR® Green and probe method qPCR. According to the purpose of the experiment, the corresponding reagents can be selected for use in conjunction with high-performance gene expression analysis.

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The post HiScript II Q RT SuperMix for qPCR (R222-01) appeared first on SEQRS Kft..

HiScript III RT SuperMix for qPCR (+gDNA wiper) is an upgraded version of HiScript II Q RT SuperMix for qPCR (+gDNA wiper), including HiScript III Reverse Transcriptase, a new generation of reverse transcriptase with optimized Buffer. This kit further improves the efficiency of cDNA synthesis, and is suitable for two-step qRT-PCR detection. The 4 × gDNA wiper Mix in the kit can remove residual genomic DNA from the RNA template, ensuring more reliable quantitative results. It simplifies qPCR primer design without the need of spanning exon junction to design primers; 5 × HiScript III qRT SuperMix contains all components required for the reverse transcription reaction and it can be started rapidly after the addition of template RNA and RNase-free ddH2O, and the gDNA wiper is terminated to ensure the integrity of the cDNA. It is compatible with dye-based and probe-based qPCR, enabling high-performance gene expression analysis.

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