
Na jaře se zúčastníme 1. československého kongresu lékařské genetiky, který se bude konat 2.-4. dubna 2025 v Kulturním a kongresovém centru Elektra v lázeňském městě Luhačovice. Tento jedinečný kong...
VíceNavštivte nás na 19. ročníku konference RANK 2025, která se koná 19. a 20. března v hotelu Zlatá Štika v Pardubicích. Konferenci pořádá Česká společnost klinické biochemie při ČLSJEP ve spolupráci s ...
VíceRádi bychom Vás pozvali na 23. Kaprasův den na téma „Klinická genetika“, který se uskuteční ve středu 26. února 2025 v Kongresovém sále Hotelu Olšanka v Praze. Těšíme se na setkání s vámi a na den pln...
VíceDescription:
RT-PCR is widely used for measuring gene expression in tissue samples or cell culture systems. Traditionally, it is performed in two separate reaction steps. First-strand cDNA is reverse-transcribed from total RNA or poly (A)+ RNA using a reverse transcriptase. Next, the cDNA is amplified by PCR using a DNA polymerase in another reaction.
The MCLAB's HoTaq Taqman probe One-step Real-time RT-PCR Kit offers a unique system for performing probe based realtime RT-PCR in a single step within a single tube with an optimized reaction condition, which utilizes our own proprietary engineered QuantumScript HD reverse transcriptase and hot-start Taq DNA Polymerase with high purity . No additional reagents or steps are required once the reaction is initialized. This novel kit enables to quantitatively detect specific RNA targets with high sensitivity, unparalleled convenience, and a wide dynamic range.
The technique reduces the risk of cross-contamination and minimizes the use of reagents. This method is particularly useful for applications in which the expression of a small number of genes that must be analyzed in many different total RNA samples, and robustly amplifing high-abundance transcripts from crude total RNA preparations.
Application:
- Gene Expression Analysis
- Genotyping
- Real-Time PCR
Primer and probe design:
To achieve the best performance, appropriate software, such as ABI Primer ExpressTM, should be used.
Recommended Reaction Conditions:
One cycle at 50°C for 10 to 30 minutes *;
One cycle at 95°C for 10 minutes;
Followed by 40 cycles of: 95°C for 15 seconds, 60°C for 1 minute #;
4°C hold (optional)
* Reaction time could be adjusted according to RNA input.
# Cycle number and annealing temperature are experiment dependent.
Recommended Storage Condition: -20°C
Notes:
To achieve accurate quantification, it is highly recommended to (1) avoid any RNase contamination; (2) design probe on sense strand; (3) use primer concentration from 100nM to 300nM; (4) shorten time between setting up reaction and loading plate onto PCR machine.
Advantages:
One-step RT-PCR products are faster.