| Catalog Number | Product | Size | Price |
|---|---|---|---|
| PB30.11-02 | UltraScript® cDNA Synthesis Kit | 25 x 20 μL Reactions | Contact us |
| PB30.11-10 | UltraScript® cDNA Synthesis Kit | 100 x 20 μL Reactions | Contact us |
| PB30.12-01 | UltraScript® Reverse Transcriptase | 10 000 Units | Contact us |
| PB30.12-04 | UltraScript® Reverse Transcriptase | 40 000 Units | Contact us |
| PB30.13-01 | UltraScript® Reverse Transcriptase (8000 U/μL) | 80 000 Units | Contact us |
| PB30.15-02 | UltraScript® cDNA Synthesis Kit Separate Oligos | 25 x 20 μL Reactions | Contact us |
| PB30.15-10 | UltraScript® cDNA Synthesis Kit Separate Oligos | 100 x 20 μL Reactions | Contact us |
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Additional Information
UltraScript® Reverse Transcriptase
UltraScript® Reverse Transcriptase is a modified reverse transcriptase (RTase) enzyme derived from MMLV, thermally stable, and highly active for cDNA synthesis. The reaction temperature can be increased up to 55 °C, providing higher specificity and efficient transcription of GC-rich RNA regions with high secondary structures. RTase is blended with an advanced RNase inhibitor to prevent RNA degradation by contaminant RNases. UltraScript® Reverse Transcriptase is not inhibited by ribosomal and transfer RNA, making synthesized RNA an ideal substrate. This enzyme is supplied with a 5x buffer containing Mg, dNTPs, stabilizers, and enhancers, optimized to produce high yield cDNA from as little as 4 pg of RNA. As oligos are not included, UltraScript® Reverse Transcriptase offers users convenience and flexibility in determining their own priming strategy depending on the analysis required. UltraScript® Reverse Transcriptase delivers exceptional performance with gene-specific primers, oligo(dT), and random hexamers to produce high-quality cDNA, ideal for numerous downstream applications. Our robust RTase is also available in a high concentration format and as a ready UltraScript® cDNA synthesis kit (formerly qPCRBIO cDNA synthesis kit), where the relative concentration of random hexamers and oligo(dT) have been optimized for cDNA production for use in real-time PCR experiments. This eliminates the need for user optimization of critical reverse transcription parameters, such as priming strategy, reverse transcriptase, buffer, and enhancers, and delivers unbiased, efficient, and sensitive cDNA synthesis every time. Read these Tips and Tricks to maximize your cDNA synthesis experiments. Learn about the best priming strategy to use depending on the starting RNA type you are using and the final application of your cDNA. For a quick summary of when each cDNA synthesis product is appropriate, use the reference table below:
| Priming Type | RNA Source | Intended Use | Suggested Product |
|---|---|---|---|
| Oligo(dT) & Random Hexamer | Any | qPCR, cloning, NGS | PB30.11/PB30.15 |
| Random Hexamer | Prokaryotic, Archaeal | qPCR, cloning, NGS | PB30.15, (PB30.12 user needs to provide primer) |
| Oligo(dT) | Eukaryotic | qPCR, cloning, NGS | PB30.15, (PB30.12 user needs to provide primer) |
| Gene-Specific Primer | Any | Targeted cloning, qPCR, NGS | PB30.12 (user needs to provide primer) |
Applications
- Random hexamers, oligo(dT), and gene-specific primers
- cDNA synthesis for real-time PCR analysis
- cDNA synthesis for PCR analysis, cloning, library preparation, and Next Generation Sequencing
- Low copy number transcripts
- Viral RNA targets
- miRNA targets
- Efficient synthesis from total RNA or poly(A)+ RNA



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