Cat #: 11-330MB
Zymo Research R2062 Direct-zol RNA MicroPrep (10µg), No TRI-Reagent, 200 Preps/Unit
Cat #: 11-330MB
Zymo Research R2062 Direct-zol RNA MicroPrep (10µg), No TRI-Reagent, 200 Preps/Unit
No TRI-Reagent
200 Preps/Unit
Brand: Zymo Research- Quick, spin column purification of high-quality total RNA (17 nt or greater) directly from TRI-Reagent®, TRIzol®, or similar.
- Bypasses messy phase separation and precipitation procedures.
- Ideal for cells, tissues, biological liquids, in vitro transcripts, etc.
- Efficient and consistent broad range purification of small and large RNAs.
- High quality RNA (A260/A280 <1.8, A260/A230 <1.8) is recovered.
- Processing Time: 10 min
- TRI Reagent® inhibits RNase activity and inactivates viruses and other infectious agents.
$785.40
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No TRI-Reagent
200 Preps/Unit
Brand: Zymo Research- Quick, spin column purification of high-quality total RNA (17 nt or greater) directly from TRI-Reagent®, TRIzol®, or similar.
- Bypasses messy phase separation and precipitation procedures.
- Ideal for cells, tissues, biological liquids, in vitro transcripts, etc.
- Efficient and consistent broad range purification of small and large RNAs.
- High quality RNA (A260/A280 <1.8, A260/A230 <1.8) is recovered.
- Processing Time: 10 min
- TRI Reagent® inhibits RNase activity and inactivates viruses and other infectious agents.
The Direct-zol RNA Kits provide a streamlined method for the purification of up to 100 µg per prep (depending on kit selected) of high-quality RNA directly from samples in TRI Reagent® or similar. Total RNA, including small RNAs (17-200 nt), is effectively isolated from a variety of sample sources (cells, tissues, serum, plasma, blood, biological liquids, etc.)
Isolation of RNA by conventional phase separation was shown to selectively enrich for some species of miRNA, leading to bias in downstream analysis. The Direct-zol method assures unbiased recovery of small RNAs including miRNA. The procedure is easy. Simply apply a prepared sample in TRI Reagent® directly to the Zymo-Spin Column and then bind, wash, and elute the RNA. No phase separation, precipitation, or post-purification steps are necessary. The eluted RNA is high quality and suitable for subsequent molecular manipulation and analysis (including RT-PCR, transcription profiling, hybridization, sequencing etc.).
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