FastStart TaqMan® Probe Master
ROCHE/FSTMPMMRO - sufficient for 100 reactions, sufficient for 500 reactions, sufficient for 2000 reactions, suitable for qPCR, suitable for RT-qPCR
Product Type: Chemical
Figure 1: Sensitive detection of an RNA template with the Transcriptor First Strand cDNA Synthesis Kit and the FastStart TaqMan® Probe Master. One hundred nanograms of total RNA (control RNA from a control kit of Supplier A) was reverse transcribed with the Transcriptor First Strand cDNA Synthesis Kit (+55 °C, 30 minutes, 20 μL final volume). The cDNA primers were specific for the GAPDH gene. A portion (2 μL) of the cDNA product was used as template in a qPCR. The PCR primers and a hydrolysis probe were also specific for the GAPDH gene. This reaction was performed twice, once with the FastStart TaqMan® Probe Master and once with a kit from another supplier. Both qPCRs were run on an Applied Biosystems 7500 Real-Time PCR System. All reactions were performed in duplicate; the ROX reference dye was included in every reaction. Result: The reactions with the Transcriptor First Strand cDNA Synthesis Kit and the FastStart TaqMan® Probe Master produced the best sensitivity.
| detection method | probe-based |
| feature | dNTPs included: no |
| hotstart | |
| input | purified DNA |
| manufacturer/tradename | Roche |
| packaging | pkg of 100 x 50 μL reactions (04673409001) |
| pkg of 2000 x 50 μL reactions (04673433001) | |
| pkg of 500 x 50 μL reactions (04673417001) | |
| Quality Level | 100  |
| technique(s) | qPCR: suitable |
| RT-qPCR: suitable | |
| usage | sufficient for 100 reactions |
| sufficient for 2000 reactions | |
| sufficient for 500 reactions |
| Application: | The FastStart TaqMan® Probe Master has been used in: • quantitative, real-time DNA-detection assays • qPCR and two-step reverse transcription (RT)-qPCR • in the hydrolysis probe detection format |
| Components: | FastStart TaqMan® Probe Master, 2x concentrated master mix that contains FastStart Taq DNA Polymerase, Reaction Buffer, and Nucleotides (dATP, dCTP, dGTP, dUTP). |
| Features and Benefits: | • Increase qPCR sensitivity and specificity: Produce lower cycle threshold (Ct) values with the hot start enzyme FastStart Taq DNA Polymerase and highest purity nucleotides included in the master mix. • Use it with any probe-based assay: Achieve sensitive, specific results in assays with the Universal ProbeLibrary Probes or any other hydrolysis probe. • Amplify and detect a broad range of DNA or cDNA targets: Amplify fragments up to 500 bp long, including those that are GC- or AT-rich. • Use with any real-time qPCR instrument other than the LightCycler® Instruments: Choose from two formulations - one that contains the ROX reference dye and one without ROX. • Visualize amplification products on agarose gels. • Use robotic pipetting stations to set up qPCR reactions: Benefit from a master mix that is stable at room temperature during extended reaction setup times. • Prevent carryover contamination: The mix contains dUTP, so that it may be used with Uracil-DNA Glycosylase to prevent false positives arising from carryover contamination (i.e., contamination with amplified DNA). |
| General description: | FastStart TaqMan® Probe Master is a ready-to-use hot start reaction mix without ROX for quantitative polymerase chain reaction (qPCR) and reverse transcription (RT)-qPCR on real-time PCR systems other than the LightCycle® instruments. It is a 2x concentrated master mix that contains all the reagents (except primers, probe, and template). This master mix simplifies the preparation of reactions for DNA detection and analysis. It allows very sensitive detection and quantification of defined DNA sequences. Hot start protocols have been also been shown to significantly improve the specificity and yield of PCR. Heat-labile blocking groups on some of the amino acid residues of FastStart Taq DNA Polymerase make the modified enzyme inactive at room temperature. Therefore, there is no elongation during the period when primers can non-specifically bind. The FastStart Taq DNA Polymerase is activated by removing the blocking groups at a high temperature (i.e., a pre-incubation step at +95°C). This FastStart TaqMan® Probe Master can be used for the amplification and detection of any DNA or cDNA target, including those that are GC- or AT-rich. However, you would need to adapt your detection protocol to the reaction conditions of the particular real-time PCR instrument used and design a specific hydrolysis probe and PCR primers for each target. Combination of this master mix with our Transcriptor First Strand cDNA Synthesis Kit achieves excellent results in two-step qRT-PCR. |
| General description: | Hot start protocols have been shown to significantly improve the specificity, sensitivity, and yield of PCR. Heat-labile blocking groups on some of the amino acid residues of FastStart Taq DNA Polymerase make the modified enzyme inactive at room temperature. Therefore, there is no elongation during the period when primers can nonspecifically bind. The FastStart Taq DNA Polymerase is activated by removing the blocking groups at a high temperature (i.e., a pre-incubation step at +95°C). |
| Legal Information: | LightCycler is a registered trademark of Roche |
| Legal Information: | TaqMan is a registered trademark of Roche Molecular Systems, Inc. |
| Other Notes: | qPCR targets In principle, the FastStart TaqMan® Probe Master can be used for the amplification and detection of any DNA or cDNA target, including those that are GC- or AT-rich. However, for each target, you would need: • to adapt your detection protocol to the reaction conditions of your real-time PCR instrument, and • design specific PCR primers and hydrolysis probes for the target. See the Operator′s Manual of your real-time PCR instrument for general recommendations. Two forms available The master mix is available in two forms – one that contains the ROX reference dye and one without ROX. Preventing carryover contamination This master contains dUTP, which will be incorporated into PCR products to help prevent false positives resulting from carryover contamination. In subsequent PCRs, you can add Uracil-DNA Glycosylase to degrade any uracil-containing carryover contaminants (amplification products from previous PCRs). qRT-PCR Combine this master mix with our Transcriptor First Strand cDNA Synthesis Kit for two-step qRT-PCR. This kit gives excellent results and works efficiently with all real-time PCR instruments. |
| Other Notes: | For life science research only. Not for use in diagnostic procedures. |
| Quality: | Function test: Each lot is tested for performance in qPCR using three templates: a GC-rich template, an AT-rich template, and a long template (approximately 440 bp). |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 1 |
| Flash Point(F) | does not flash |
| Flash Point(C) | does not flash |
| UNSPSC | 41106300 |