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TransScript® All-in-One First-Strand cDNA Synthesis SuperMix for qPCR (One-Step gDNA Removal )&lt

TransScript® All-in-One First-Strand cDNA Synthesis SuperMix for qPCR (One-Step gDNA Removal )&lt

Item no.	TRG-AT341-03
Manufacturer	TransGen Biotech
Amount	500 rxns x 20 ul system
Quantity options	50 rxns x 20 ul system 100 rxns x 20 ul system 500 rxns x 20 ul system
Category	Nucleic Acids DNA cDNA
Type	Reagents
Specific against	other
Dry ice	Yes
Citations	1 Sun X, Zhang T, Tong B, et al. POGZ suppresses 2C transcriptional program and retrotransposable elements[J]. Cell Reports, 2023.(IF 8.80) 2 Yuan F, Cai J, Wu J, et al. Z-DNA binding protein 1 promotes heatstroke-induced cell death[J]. Science, 2022.(IF 47.72) 3 Yuan F, Cai J, Wu J, et al. Z-DNA binding protein 1 promotes heatstroke-induced cell death[J]. Science, 2022.(IF 63.71) 4 Yu Z, Deng P, Chen Y, et al. Inhibition of the PLK1‐coupled cell cycle machinery overcomes resistance to oxaliplatin in colorectal cancer[J]. Advanced Science, 2021.(IF 16.80) 5 Sun X, Peng X, Cao Y, et al. ADNP promotes neural differentiation by modulating Wnt/β-catenin signaling[J]. Nature communications, 2020.(IF 12.12) 6 Wu H, Qu X, Dong Z, et al. WUSCHEL triggers innate antiviral immunity in plant stem cells[J]. Science, 2020.(IF 41.84) 7 Ji S, Luo Y, Cai Q, et al. LC domain-mediated coalescence is essential for Otu enzymatic activity to extend Drosophila lifespan[J]. Molecular cell, 2019.(IF 14.20)
ECLASS 10.1	42051003
ECLASS 11.0	42051003
UNSPSC	12000000
Available
Manufacturer - Applications	Multiple copy and low copy gene detection
Manufacturer - Category	RT-PCR
Storage Conditions	at -20 °C for two years
Product Details	The kit provides all the necessary components for cDNA synthesis from total RNA or mRNA. It is provided at 5× concentration and used at 1× concentration by adding gDNA remover, RNA and H2O. Simultaneous genomic DNA removal and cDNA synthesis are performed. After cDNA synthesis, gDNA remover and reverse transcriptase are inactivated by heating at 85℃ for 5 seconds. The resulting cDNA is suitable for qPCR, not for regular PCR. • Simultaneous genomic DNA removal and cDNA synthesis. • The optimal ratio of oligo(dT)18 primer to random primer(N9) for qPCR ready cDNA. • qPCR ready cDNA in 15 minutes. • cDNA up to 250 bp. Applications Multiple copy and low copy gene detection Storage at -20 ℃ for two years Shipping Dry ice (-70 ℃)

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.