TRIzol® LS Reagent

TRIzol® LS Reagent

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  • ¥2665
  • Ambion
  • 进口
  • 10296-010
  • 2025年07月16日
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    • 详细信息
    • 询价记录
    • 技术资料
    • 保存条件

      Room Temperature

    • 英文名

      Downstream Application: Reverse Transcriptase PCR (RT-PCR), Cloning, Real-Time Quantitative PCR (qPCR), Nuclease Protection Assays, cDNA Library Construction, Northern Blotting

    • 规格

      100 mL

    描述

    TRIzol® LS Reagent is a complete, ready-to-use reagent optimized for the isolation of high-quality total RNA, or the simultaneous isolation of RNA, DNA, and protein from a variety of liquid samples. This monophasic solution of phenol and guanidine isothiocyanate is designed to isolate separate fractions of RNA, DNA, and proteins from liquid samples of human, animal, plant, yeast, bacterial, and viral origin, typically within one hour.

    • Formulated for use with liquid samples such as serum and virus preparations
    • Facilitates recovery of RNA, DNA, and protein from a single liquid sample
    • Offers excellent lysis capability, even with difficult biological fluids

    Reliably Purify RNA from Multiple Sample Sources
    TRIzol® LS Reagent is designed for processing a variety of liquid samples of up to 0.25 ml in volume. TRIzol® LS Reagent differs from the standard TRIzol® Reagent in concentration, which permits larger samples to be processed. Just as with the standard TRIzol® Reagent, the integrity of resulting RNA preparations is maintained by the highly effective inhibition of RNase activity during sample homogenization. The simplicity of the TRIzol® LS Reagent method allows simultaneous processing of a large number of samples. The entire procedure can be completed in 1 hour. Total RNA isolated by TRIzol® LS Reagent is free of protein and DNA contamination.

    Formulated to Serve Multiple Isolations
    TRIzol® LS Reagent allows you to perform sequential precipitation of RNA, DNA, and proteins from a single sample. After homogenizing the sample with TRIzol® LS Reagent, chloroform is added, and the homogenate is allowed to separate into a clear upper aqueous layer (containing RNA), an interface, and a red lower organic layer (containing the DNA and proteins). RNA is precipitated from the aqueous layer with isopropanol. DNA is precipitated from the aqueous/organic interface with ethanol. Protein is precipitated from the phenol-ethanol layer by isopropanol precipitation. The precipitated RNA, DNA, or protein is washed to remove impurities, and then resuspended for use in downstream applications.

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