Products
The QIAGEN OneStep RT-PCR Kit is intended for molecular biology applications. This product is not intended for the diagnosis, prevention, or treatment of a disease.
QIAGEN OneStep RT-PCR Kit (100)
Cat. No. / ID: 210212
For 100 x 50 µl reactions: QIAGEN OneStep RT-PCR Enzyme Mix (1 x 200 µl), 5x QIAGEN OneStep RT-PCR Buffer (1 x 1 ml), dNTP Mix (1 x 200 µl, 10 mM each), 5x Q-Solution (1 x 2 ml), RNase-Free Water (2 x 1.9 ml)
This product contains substances regulated under REACH (EC 1907/2006 Annex XIV). The use of this product in the EU is permitted subject to an exemption (Article 56(3)). Please refer to the REACH notification and the SDS of this product, both of which can be found in the “Resources” section of this page, for more information.
QIAGEN OneStep RT-PCR Kit (1000)
Cat. No. / ID: 210215
For 1000 x 50 µl reactions (available in a single tube): QIAGEN OneStep RT-PCR Enzyme Mix (2 x 1 ml), 5x QIAGEN OneStep RT-PCR Buffer (1 x 10 ml), dNTP Mix (2 x 1 ml, 10 mM each), 5x Q-Solution (1 x 10 ml), RNase-Free Water (1 x 40 ml)
This product contains substances regulated under REACH (EC 1907/2006 Annex XIV). The use of this product in the EU is permitted subject to an exemption (Article 56(3)). Please refer to the REACH notification and the SDS of this product, both of which can be found in the “Resources” section of this page, for more information.
QIAGEN OneStep RT-PCR Kit (25)
Cat. No. / ID: 210210
For 25 x 50 µl reactions: QIAGEN OneStep RT-PCR Enzyme Mix (1 x 50 µl), 5x QIAGEN OneStep RT-PCR Buffer (1 x 250 µl), dNTP Mix (1 x 50 µl, 10 mM each), 5x Q-Solution (1 x 400 µl), RNase-Free Water (1 x 1.9 ml)
This product contains substances regulated under REACH (EC 1907/2006 Annex XIV). The use of this product in the EU is permitted subject to an exemption (Article 56(3)). Please refer to the REACH notification and the SDS of this product, both of which can be found in the “Resources” section of this page, for more information.
Features
- Fast and easy one-tube setup
- Efficient one-step RT-PCR of any RNA template without optimization
- Unique enzyme mix for high specificity and sensitivity
- Balanced mixture of enzymes with optimized reverse-transcription buffer
Product Details
The QIAGEN One-Step RT-PCR Kit provides a blend of Sensiscript and Omniscript Reverse Transcriptases, HotStarTaq DNA Polymerase, QIAGEN OneStep RT-PCR Buffer, a dNTP mix, and Q-Solution, a novel additive that enables efficient amplification of "difficult" (e.g., GC-rich) templates. The easy one-tube setup and optimized components result in highly sensitive and successful results.
Performance
The QIAGEN OneStep RT-PCR Kit provides a convenient format for highly sensitive and specific RT-PCR using any RNA template. The kit includes optimized components that allow both reverse transcription and PCR amplification to take place in the same reaction mix in a "one-step" reaction. A unique enzyme combination and specially developed reaction buffer ensure efficient, highly specific reverse transcription and PCR in one tube, without the need for optimization (see figures " Highly specific RT-PCR using low amounts of template" and " Efficient detection of viral RNA"). The innovative, dual-cation PCR buffer provided with the kit ensures high yields of specific PCR product over a wide range of annealing temperatures (see figure " Influence of annealing temperature on specificity"). Suboptimal RT-PCR is improved using Q-Solution, a unique additive that facilitates reverse transcription and amplification of templates with a high GC content or a high degree of secondary structure (see figure " RT-PCR of GC-rich template").
See figures
Principle
The QIAGEN OneStep RT-PCR Kit is designed for easy and sensitive one-step RT-PCR using any RNA template.
The QIAGEN OneStep RT-PCR Enzyme Mix contains a specially formulated enzyme blend for both reverse transcription and PCR. The unique combination of Omniscript and Sensiscript Reverse Transcriptases, with their high affinity for RNA templates, ensures highly efficient and sensitive transcription of RNA amounts from as little as 1 pg up to 2 µg. After reverse transcription, reactions are heated to 95°C for 15 minutes to activate HotStarTaq DNA Polymerase and simultaneously inactivate the reverse transcriptases. This hot-start step eliminates nonspecific amplification products such as primer dimers and reduces background smear, ensuring highly sensitive and reproducible RT-PCR (see figures " Highly specific RT-PCR using low amounts of template" and " Efficient detection of viral RNA").
Wide range of annealing temperatures
The optimal primer annealing temperature is dependent on the base composition (i.e., the proportion of A, T, G, and C nucleotides), primer concentration, and ionic reaction environment. QIAGEN PCR Buffers contain both K+ and NH4+ and deliver high yields of specific PCR product over a wide range of annealing temperatures (see figure " Increased specific primer annealing"). This specificity is achieved by destabilizing non-specifically bound primers, providing a more robust reaction environment and eliminating the need for tedious annealing temperature optimization. In contrast, the range of optimal PCR annealing temperatures is smaller and less predictable using a PCR or one-step RT-PCR buffer that only contains K+, as illustrated in figure " Influence of annealing temperature on specificity".
QIAGEN OneStep RT-PCR Buffer has been specially developed to allow both efficient reverse transcription and PCR amplification. The buffer contains novel additives that prevent inhibition of PCR amplification by reverse transcriptases, a problem often encountered in one-step RT-PCR. The buffer ensures specific primer annealing over a wide range of temperatures and Mg2+ concentrations; providing robust and highly efficient RT-PCR from any RNA template. The QIAGEN OneStep RT-PCR Kit includes Q-Solution, an innovative additive that modifies the melting behavior of nucleic acids. Q-Solution facilitates reverse transcription and amplification of templates with a high GC content or a high degree of secondary structure (see figure " RT-PCR of GC-rich template"). Using Q-Solution simplifies optimization of RT-PCR for difficult templates. The QIAGEN OneStep RT-PCR Kit includes everything required for faster and easier RT-PCR for even the most sensitive applications (see table).
| QIAGEN OneStep RT-PCR Kit contents | Features |
|---|---|
| HotStarTaq DNA Polymerase | Highly specific products |
| Sensiscript and Omniscript Reverse Transcriptases | Wide range of RNA amounts (1 pg – 2 µg) High sensitivity |
| OneStep RT-PCR Buffer | Minimal optimization needed No inhibition of PCR by reverse transcriptases Inhibition of RNases |
| Q-Solution | Facilitates amplification of GC-rich templates |
See figures
Procedure
The QIAGEN OneStep RT-PCR Kit allows fast and easy RT-PCR setup. Whatever the application — virus detection, molecular diagnostics research, or gene expression analysis — just mix all components together in one tube and start the thermal-cycler program (see flowchart " OneStep RT-PCR procedure"). The reaction mixture contains all of the reagents required for both reverse transcription and PCR; nothing needs to be added once the reaction has been started (see table).
See figures
Applications
The QIAGEN OneStep RT-PCR Kit is suitable for RT-PCR applications such as:
- Virus detection
- Single-cell RT-PCR
- Gene-expression analysis
Supporting data and figures
OneStep RT-PCR procedure.
The QIAGEN OneStep RT-PCR Kit allows fast and easy RT-PCR setup. Whatever the application — virus detection, molecular diagnostics research, or gene expression analysis— just mix all components together in one tube and start the thermal-cycler program. The reaction mixture contains all of the reagents required for both reverse transcription and PCR; nothing needs to be added once the reaction has been started.
Specifications
| Features | Specifications |
|---|---|
| Applications | Gene-expression analysis, virus detection |
| Mastermix | No |
| Enzyme activity | Reverse transcription, 5' -> 3' exonuclease activity |
| Reaction type | One-step RT-PCR |
| Real-time or endpoint | Endpoint |
| Sample/target type | RNA template |
| Single or multiplex | Single |
| With/without hotstart | With hotstart |
Resources
Supplementary Protocols (6)
Brochures & Guides (3)
Kit Handbooks (1)
Quick-Start Protocols (1)
Safety Data Sheets (4)
Technical Information (1)
Certificates of Analysis (1)
Publications
Up-regulation of cyclooxygenase-2 expression is involved in R(+)-methanandamide-induced apoptotic death of human neuroglioma cells.
Mol Pharmacol; 2004; 66 (6):1643-51 2004 Sep 10 PMID:15361550
Drosophila crinkled, mutations of which disrupt morphogenesis and cause lethality, encodes fly myosin VIIA.
Genetics; 2004; 168 (3):1337-52 2004 Nov PMID:15579689
Instability of the restriction fragment length polymorphism pattern of open reading frame 5 of porcine reproductive and respiratory syndrome virus during sequential pig-to-pig passages.
J Clin Microbiol; 2004; 42 (10):4462-7 2004 Oct PMID:15472294
Expression of growth differentiation factor 9 messenger RNA in porcine growing and preovulatory ovarian follicles.
Biol Reprod; 2004; 71 (4):1290-5 2004 Jun 9 PMID:15189836
Effect of vaccine use in the evolution of Mexican lineage H5N2 avian influenza virus.
J Virol; 2004; 78 (15):8372-81 2004 Aug PMID:15254209
FAQ
Are there specific recommendations for performing RT-PCR on RNA isolated from paraffin-embedded samples?
Do I need to use an RNase inhibitor in my RT reaction?
Is mRNA isolation necessary for sensitive RT-PCR?
Does QIAGEN sell Q-Solution separately?
Do you have a protocol for polyacrylamide gel analysis of oligonucleotides?
Does the 5x OneStep RT-PCR Buffer contain BSA?
Can I shorten the activation time for the HotStarTaq DNA Polymerase?