Набор Sanshibio One Step RT-qPCR (Зонд)

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Описание

Набор One Step RT-qPCR (Зонд)

предмет номерER101 Спецификация:50T/100T Storage: Store at -20°C

Внедрение продукции

This product is a specialized reagent for one-step reverse transcription-real-time fluorescence quantitative ПЦР (RT-qPCR) using the probe method. Performing One Step RT-qPCR reactions with this product allows for continuous processing within the same reaction tube, simplifying the procedure and avoiding cross-contamination between samples while enhancing detection sensitivity. This assay kit employs a novel reverse transcriptase (HI-MMLV Reverse Transcriptase), a newly designed antibody-modified hot-start Taq DNA polymerase, and RNase Inhibitor in the form of the One Step RT-qPCR Enzyme Mix. It features enhanced RNA affinity, термическая стабильность, higher amplification efficiency, and specificity. This enables the generation of robust standard curves within a wide quantitative range, facilitating accurate quantification of various target genes at different expression levels. It offers good repeatability and high reliability.

Содержание продукта:

КомпонентыER101-01(50T)ER101-02(100T)
One Step RT-qPCR Enzyme Mix50мкл100мкл
5× One Step RT-qPCR Master Mix250мкл500мкл
RNase-Free ddH2О1мл2× 1mL

Хранилище:

Store at -20°C, with a minimum shelf life of 12 месяцы.

Activity Definition:

Using activated mahi-mahi sperm DNA as template/primer, the activity is defined as 1 unit (ты) of acid-insoluble material incorporated, by taking up 10 nmol of nucleotides within 30 minutes at 74°C.

Product Uses:

This assay kit is suitable for probe-based one-step reverse transcription-real-time fluorescence quantitative PCR. It allows accurate and straightforward analysis of RNA expression, particularly well-suited for detecting small amounts of RNA. It is compatible with various types of fluorescence quantitative PCR instruments.

ПримечаниеFor certain companiesReal-Time PCR amplification instruments that exhibit inter-well fluorescence signal discrepancies, please either prepare or contact the manufacturer to acquire ROX Reference Dye to correct these errors. Detailed specifics should be chosen based on experimental design, instrument manuals, or the specific usage requirements of various fluorescent probes.

Кроме того, this assay kit does not include a gDNA (геномная ДНК) removal component. If your experiment requires freedom from gDNA interference, please conduct a gDNA removal step during or after экстракция РНК and then proceed with the experiment using this assay kit. This precaution will prevent any potential interference with your experimental results.

Operating steps:

  1. Prepare the following reaction mixture in RNase-Free centrifuge tubes:
ReagentsUsage AmountFinal Concentration
One Step RT-qPCR Enzyme Mix1мкл
5× One Step RT-qPCR Master Mix5мкл
Forward Primer (10µM)0.5-2.5мкл0.2-1.0мкМ
Reverse Primer (10µM)0.5-2.5мкл0.2-1.0мкМ
Зонд (10µM)0.25-1мкл
Total RNA1pg-1µg
RNase-Free ddH2ОUp to 25µL

Примечание:The amounts of each component can be adjusted according to actual needs.

  • Perform the One Step RT-qPCR reaction under the following conditions:
Method/StepsСtandard Procedureвопросuick ProcedureCycles
50℃15мин10мин1
95℃3мин1мин1
95℃15с45Cycles
60℃30с20с
  • После завершения реакции, verify the amplification curve of the Real Time PCR instrument and analyze the results.

Меры предосторожности:

  1. The One Step RT-qPCR Enzyme Mix contains a high concentration of glycerol. Перед использованием, please briefly centrifuge the mix to collect it at the bottom of the reaction tube. Gently pipette up and down to mix thoroughly. For reaction setup, use RNase-Free pipette tips, EP tubes, и т. д., and avoid contamination as much as possible.
  2. Обычно, a primer final concentration of 0.2 µM is sufficient for optimal amplification. When the reaction performance is suboptimal, adjust the primer concentration within the range of 0.1 к 1.0 µM. Probe concentration can be adjusted between 50 nM and 250 nM. qPCR is highly sensitive, and the accuracy of template amount during reaction setup greatly influences the final quantification results. It is recommended to dilute the template (например, dilute 2-5 µL of sample) before adding it to the reaction mix to enhance experimental reproducibility.
  3. Choose an amplification product length within the range of 80 б.п. до 200 б.п.. For templates with complex secondary structures and high GC regions, raising the reverse transcription temperature to 55°C can improve amplification efficiency and detection sensitivity.
  4. Verify whether the actual Real Time PCR instrument used supports fast amplification cycles. For initial attempts, conduct preliminary experiments to confirm. Adjust the extension time according to the shortest data collection time limit required by the specific Real Time PCR instrument used. For instruments like ABI 7700 and ABI 7900, use at least 30 секунды. For ABI 7000 and ABI 7300, use at least 31 секунды. For ABI 7500, use at least 34 секунды. If using the ABI series of Real Time PCR instruments, include ROX Reference dye in the solution preparation.

Подробности

размер

50Т, 100Т

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