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HiScript II Q RT SuperMix for qPCR
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 RT SuperMix for qPCR is specially designed for 2-step RT-qPCR. The 5× Mix contains all necessary components needed for reverse transcription, including Buffer, dNTPs, HiScript II Reverse Transcriptase, RNase inhibitor, and Random primers/Oligo-dT primer mix.
HiScript II 1st Strand cDNA Synthesis Kit
M-MLV(H-) Reverse Transcriptase
ChamQ Geno-SNP Probe Master Mix
ChamQ Geno-SNP Probe Master Mix is specially designed for single-nucleotide polymorphism (SNP) typing by probe method
ChamQ Universal SYBR® qPCR Master Mix
Vazyme ChamQ Universal SYBR ® qPCR Master Mix, protected by Champagne Taq DNA Polymerase (Vazyme, #P122) via an antibody-modified hot-start activation technique, is specially designed for SYBR Green I based quantitative PCR (qPCR)
AceQ U+ Universal Probe Master Mix V2
AceQ Universal SYBR® qPCR Master Mix
AceQ ® Universal SYBR Green qPCR Master Mix utilizes a special performance-enhanced Taq DNA polymerase protected via a hot-start activation technique, and optimized qPCR buffer system to perform SYBR Green I based quantitative PCR (qPCR)
HiScript II U+ One Step qRT-PCR Probe Kit
HiScript II One Step qRT-PCR Probe Kit
HiScript II One Step qRT-PCR SYBR® Green Kit
The Vazyme HiScript II One Step qRT-PCR SYBR Green Kits are designed for SYBR Green I-based qPCRs that directly use RNA as templates. The reverse transcription and PCR can be finished in one tube, significantly reducing pipetting procedures and the risk of contamination. The HiScript II Reverse Trancriptase and Champagne Taq DNA Polymerase contained in this kit and an optimized buffer system enables high-sensitive total RNA detection (as little as 1 pg).
AceQ U+ Probe Master Mix
AceQ qPCR Probe Master Mix
AceQ qPCR SYBR® Green Master Mix
AceQ qPCR SYBR Green Master Mix utilizes a special performance-enhanced Taq DNA polymerase protected via a hot-start activation technique, and optimized qPCR buffer system to perform SYBR Green I based quantitative PCR (qPCR).