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Picture of Transcriptor High Fidelity cDNA Synthesis Kit

Transcriptor High Fidelity cDNA Synthesis Kit

Transcriptor High Fidelity Reverse Transcriptase enzyme blend for high fidelity two-step RT-PCR of RNA up to 14 kb.

For life science research only. Not for use in diagnostic procedures.

Product No. Pack Size List Price Your Price Quantity
05081955001
50 reactions $ 360.00

Product No. Pack Size List Price Your Price Quantity
05091284001
100 reactions $ 652.00

Product No. Pack Size List Price Your Price Quantity
05081963001
200 reactions $ 1,171.00

The core component of the kit is the Transcriptor High Fidelity Reverse Transcriptase, a blend of a recombinant reverse transcriptase and a proofreading mediating enzyme. The synergy between both enzymes is the key to the ability of the enzyme blend to reverse transcribe RNA templates with 7-fold higher fidelity compared to other commonly used reverse transcriptases.
The Transcriptor High Fidelity Reverse Transcriptase enzyme blend efficiently reverse transcribes templates up to 14 kb. Due to the high thermostability of both enzyme components and the specially optimized buffer system, reverse transcription is possible at temperatures up to +55°C. This allows the reverse transcription of GC-rich templates with high secondary structure, without the need to include additives that may negatively influence the accuracy of the reverse transcription reaction.
The recombinant reverse transcriptase included in the enzyme blend is expressed in E. coli. The enzyme has RNA-directed DNA polymerase activity, DNA-dependent DNA polymerase activity, unwinding activity and RNase H activity that degrades RNA in RNA:DNA hybrids. The latter circumvents the need to perform an additional time-consuming RNase H incubation step after reverse transcription, reducing reaction time and costs.
The kit provides all reagents required for first-strand cDNA synthesis reactions. For priming, three different primer systems can be used. Two cDNA synthesis primers are provided with the kit: random hexamer primers and an anchored-oligo(dT)18 primer. The latter is designed to bind at the beginning of the poly(A) tail to generate full-length cDNAs and to prevent priming from internal sites of the poly(A) tail. The 5' ends of long mRNAs are often underrepresented, therefore this priming method is preferred for most applications. The use of random hexamer primers enables priming throughout the length of RNA for uniform representation of all RNA sequences and allows reverse transcription of RNAs that do not carry a poly(A) tail. The thermostable Protector RNase Inhibitor (included in the kit) protects RNA from degradation at high reaction temperatures.


Increase accuracy during reverse transcription reactions.

  • Benefit from an optimized enzyme blend with 7-fold higher fidelity compared to other commonly used reverse transcriptases (Figure 1).
  • Rely on true-fidelity data, as determined by the sequencing of several million bases with the Genome Sequencer 20 System.

Combine accuracy with high sensitivity, high yield, and full-length transcripts.

  • Generate full-length transcripts up to 14 kb with the anchored-oligo (dT)18 primers included in the kit (Figure 2).
  • Obtain excellent yields.
  • Detect low-copy number templates; reverse transcribe from as little as 10 pg template RNA (Figure 3).
  • Transcribe a variety of templates, even the most difficult ones (e.g., GC-rich RNAs with high secondary structure) at temperatures up to +55°C.

Get results faster.

  • Reduce reverse transcription reaction time to as little as 10 minutes (Figure 4).
  • Be first to finish (Figure 5). 

Contents

  1. Transcriptor High Fidelity Reverse Transcriptase (blend of a recombinant reverse transcriptase and a proofreading mediating enzyme)
  2. Transcriptor High Fidelity Reaction Buffer, 5x concentrated
  3. Protector RNase Inhibitor
  4. dNTP mix, PCR Grade
  5. Anchored-oligo (dT)18Primer
  6. Random Hexamer Primer
  7. DTT
  8. Water, PCR Grade
  9. Control RNA – total RNA fraction purified from the immortalized cell line K-562*
  10. Control PBGD primer mix (forward and reverse primer)*

* Included only in the 50-reaction pack size.

The Transcriptor High Fidelity cDNA Synthesis Kit is designed to reverse transcribe RNA with increased fidelity compared to other reverse transcriptases. The kit features Transcriptor High Fidelity Reverse Transcriptase, a blend of a recombinant reverse transcriptase and a proofreading mediating enzyme optimized for two-step RT-PCR, making this the product of choice for:

  • Cloning genes of interest
  • Sequencing transcriptomes
  • Generating cDNA libraries with large and full-length inserts
  • Generating gene expression analysis, like RNA splicing analysis.

As the kit is also tested with the LightCycler® Instruments and other real-time PCR instruments, the product is also ideal for quantitative RT-PCR applications that require high fidelity.
The kit contains all components required for synthesizing cDNA suitable for direct use in qualitative RT-PCR with conventional thermal cyclers or quantitative RT-PCR on real-time PCR instruments. The 50-reaction pack size also includes 10 control reactions (control RNA and control primer mix).

 

Accuracy of the Transcriptor High Fidelity Reverse Transcriptase and a commonly used M-MuLV Reverse Transcriptase.

Figure 1: Accuracy of the Transcriptor High Fidelity Reverse Transcriptase and a commonly used M-MuLV Reverse Transcriptase.
Error rate was determined by sequencing using the Genome Sequencer 20 System. RNA was reverse transcribed with the Transcriptor High Fidelity Reverse Transcriptase and a commonly used M-MuLV reverse transcriptase. After purification of the cDNA and amplification with a proofreading polymerase, the error rate of the reverse transcriptases was calculated by subtracting the error rate of the PCR control performed with plasmid DNA carrying the same sequence. The error rate of the Transcriptor High Fidelity ReverseTranscriptase is a mean value of four independent experiments in which at least 3.1 x 106 bases were sequenced. For the M-MuLV reverse transcriptase, 4.5 x 106 bases were sequenced.
Accuracy is represented as error rate -1, the average number of bases that are successfully reverse transcribed before a single transcription error is made. Transcriptor High Fidelity Reverse Transcriptase shows higher accuracy than a standard M-MuLV reverse transcriptase, resulting in lower error rate during cDNA synthesis.


Comparison of different reverse transcriptases for the reverse transcription of total RNA for different fragment sizes

Figure 2: Comparison of different reverse transcriptases for the reverse transcription of total RNA for different fragment sizes.
Total RNA (1 μg from human muscle total RNA for the 2.3 kb fragment; 1 μg from HeLa total RNA for the 5.4 kb and 9.4 kb fragments; 2 μg of rat brain total RNA for the 12.4 kb fragment) was reverse transcribed with different reverse transcriptases, according to the manufacturers' recommendations. A 5 μl aliquot of each cDNA reaction was subsequently amplified with Roche's Expand Long Range dNTPack. Results show that the Transcriptor High Fidelity cDNA Synthesis Kit efficiently transcribes a broad range of fragment sizes with greater yield and specificity compared to the reverse transcriptases from other suppliers.


Comparison of different incubation times for cDNA reactions, using the Transcriptor High Fidelity cDNA Synthesis Kit.

Figure 3: Comparison of different incubation times for cDNA reactions, using the Transcriptor High Fidelity cDNA Synthesis Kit.
One microgram of HeLa total RNA was reverse transcribed at +50°C for the times indicated. Five-microliter aliquots of the cDNA reactions were amplified with primers for an 8.5 kb fragment, using Roche’s Expand Long Range dNTPack. All reactions were performed in duplicate. Results show that the Transcriptor High Fidelity cDNA Synthesis Kit efficiently transcribes RNA with high speed and accuracy.
Comparison of different incubation times for cDNA reactions, using the Transcriptor High Fidelity cDNA Synthesis Kit

Figure 4: Comparison of different incubation times for cDNA reactions, using the Transcriptor High Fidelity cDNA Synthesis Kit.
1 µg of HeLa total RNA was reverse transcribed at +50°C for the times indicated. 5 µl aliquots of the cDNA reactions were amplified with primers for an 8.5 kb fragment, using Roche's Expand Long Range dNTPack. All reactions were performed in duplicate.

First to finish with Transcriptor High Fidelity cDNA Synthesis Kit.
Figure 5: First to finish with Transcriptor High Fidelity cDNA Synthesis Kit.
Reduce the total reaction time by around 1 hour with Transcriptor High Fidelity cDNA Synthesis Kit compared to Supplier I's cDNA Synthesis Kit including RNase H- M-MuLV.



Store the cDNA after synthesis up to 1 hour at room temperature without loosing performance

Figure 6:  Store the cDNA after synthesis up to 1 hour at room temperature without loosing performance.

Amplification of difficult templates over the whole temperature range

Figure 7: Amplification of difficult templates over the whole temperature range.
GC-rich RNA with a GC-content of 74% were reverse transcribed at different temperatures with Transcriptor High Fidelity cDNA Synthesis Kit. A 5 µl aliquot of each cDNA reaction was subsequently amplified with Roche Applied Science's Expand Long Template PCR System.

Retroviral reverse transcriptases commonly used for cDNA synthesis exhibit a higher error rate than other DNA polymerases used in nucleic acid analysis techniques. This lack in accuracy leads to a significant number of base exchanges or frameshifts, which are further propagated in subsequent PCR reactions. High fidelity (proofreading) PCR enzymes have been available for many years; Roche’s new high accuracy reverse transcriptase is further able to synthesize high yields of full-length cDNA.
High mutation rate is a hallmark of retrovirus replication. This originates in the mechanism of genome replication by the viral-encoded reverse transcriptase, which converts the genomic RNA of the virus to a dsDNA. During this process, reverse transcription produces frequent replication errors. One accepted explanation of this inaccuracy is the lack of RT 3’-5’ exonuclease activity. The naturally high error rate of reverse transcriptases is not optimal for many different applications.
 

Quality

Each lot of the kit is function tested in an assay to quantify proofreading activity and in a two-step qRT-PCR assay to quantify the presence of PBGD mRNA in total RNA from K-562 cells.

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