Real-time fluorescence-enabled RPA (exo probes)
2× lyophilized master mix supports real‑time detection via exo probes at 37–42 °C with minimal hands‑on time. Ideal for rapid DNA target quantification and workflow integration with standard instruments.
| Product Number | MM32RPAEXO |
| Function | RPA with exonuclease and fluorescent probes |
| For Use In | Real-Time DNA target quantification |
| Source | Recombinant E. coli |
| Shipping Conditions | Ambient |
| Storage Temperature | Ambient |
| Stability | ≥12 months |
| Delivery Format | Tubes |
| Intended Use | This product is for research use only |
Synthego’s Reverse Transcriptase is a genetically engineered M-MuLV Reverse Transcriptase designed for exceptional performance in cDNA synthesis and RT-PCR applications. With increased thermostability and reduced RNase H activity, our engineered M-MuLV delivers high yields of full-length cDNA, even for longer templates, making it a reliable choice for demanding workflows.
This ultrapure enzyme is free of RNases and nucleases, ensuring optimal reaction conditions and preventing degradation of RNA templates. It is active at temperatures up to 55°C, enabling first-strand cDNA synthesis at higher temperatures, which improves specificity and reduces secondary structure interference. It is ideal for both two-step and one-step RT-PCR and qRT-PCR, offering superb sensitivity and specificity, even with low template inputs.
Exonuclease assay
Linearized lambda/HindIII fragments are incubated with the Reverse Transcriptase in a 50 µl reaction mixture for 4 hours at 37 °C. No degradation of DNA was observed.
Endonuclease/Nick Activity
Supercoiled plasmid DNA is incubated with the enzyme in a 50 µl reaction mixture for 4 hours at 37 °C. No conversion of covalently closed circular DNA to nicked DNA detected.
Contamination with E. coli DNA
Absence of E. coli genomic DNA is confirmed by qPCR using a sample of the enzyme and specific primers targeting the E. coli 16S rRNA gene. No contamination detected.
RNase Assay
An RNA template is incubated with the enzyme in a 20 µl reaction mixture for 1 hour at 42 °C. No RNA degradation observed.
Functional Assay
cDNA synthesis with oligo(dT) and/or hexamer primers, followed by PCR.
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