サンシビオ ワンステップRT-qPCRキット (プローブ)

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説明

ワンステップ RT-qPCR キット (プローブ)

商品番号ER101 仕様:50T/100T Storage: -20℃で保存

製品導入

This product is a specialized reagent for one-step reverse transcription-real-time fluorescence quantitative PCR (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, thermal stability, higher amplification efficiency, そして特異性. 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.

商品内容:

コンポーネント ER101-01(50T) ER101-02(100T)
One Step RT-qPCR Enzyme Mix 50μL 100μL
5× One Step RT-qPCR Master Mix 250μL 500μL
RNase-Free ddH2 1mL 2×1ml

ストレージ:

-20℃で保存, 最低保存期間は 12 月.

アクティビティの定義:

活性化されたマヒマヒ精子 DNA をテンプレート/プライマーとして使用する, アクティビティは次のように定義されます 1 ユニット (U) 酸不溶性物質が組み込まれている, 取り上げることで 10 ヌクレオチドの nmol 30 74℃で5分.

製品の用途:

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.

注記For 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.

さらに, this assay kit does not include a gDNA (ゲノムDNA) removal component. If your experiment requires freedom from gDNA interference, please conduct a gDNA removal step during or after RNA抽出 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:
試薬 Usage Amount 最終濃度
One Step RT-qPCR Enzyme Mix 1μL
5× One Step RT-qPCR Master Mix 5μL
Forward Primer (10μM) 0.5-2.5μL 0.2-1.0μM
Reverse Primer (10μM) 0.5-2.5μL 0.2-1.0μM
プローブ (10μM) 0.25-1μL
Total RNA 1pg-1µg
RNase-Free ddH2 Up to 25µL

注記:各成分の量は実際のニーズに応じて調整できます.

  • Perform the One Step RT-qPCR reaction under the following conditions:
方法・手順 Standard procedure Quick procedure サイクル
50℃ 15分 10分 1
95℃ 3分 1分 1
95℃ 15s 5s 45サイクル
60℃ 30s 20s
  • After the reaction is completed, verify the amplification curve of the Real Time PCR instrument and analyze the results.

予防:

  1. The One Step RT-qPCR Enzyme Mix contains a high concentration of glycerol. ご使用の前に, 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, 等, and avoid contamination as much as possible.
  2. 通常, 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 に 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 (例えば, 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 bp to 200 血圧. 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 秒. For ABI 7000 and ABI 7300, use at least 31 秒. For ABI 7500, use at least 34 秒. If using the ABI series of Real Time PCR instruments, include ROX Reference dye in the solution preparation.

追加情報

サイズ

50T, 100T

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