Cat #: 11-330H
Zymo Research R2054 Direct-zol-96 RNA (10µg/well), 96-Well, No TRI-Reagent, 2 x 96 Preps/Unit
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Cat #: 11-330H
Zymo Research R2054 Direct-zol-96 RNA (10µg/well), 96-Well, No TRI-Reagent, 2 x 96 Preps/Unit
96-Well, No TRI-Reagent
2 x 96 Preps/Unit
Brand: Zymo Research- Quick, 96-well purification of high-quality total RNA directly from TRIzol®, TRI Reagent®, or similar
- Bypasses phase separation and precipitation procedures
- RNA is eluted into as little as 10 µl DNase/RNase-free water. DNase I included for DNA-free RNA
- The RNA binding capacity of the Zymo-Spin I-96 Plate is 10 µg/well
- A260/A280 > 1.8, A260/A230 > 1.8. Complete removal of DNA can be performed with DNase I digestion
- TRI Reagent® provided only with cat# 11-330HT and 11-331HT
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$584.55
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96-Well, No TRI-Reagent
2 x 96 Preps/Unit
Brand: Zymo Research- Quick, 96-well purification of high-quality total RNA directly from TRIzol®, TRI Reagent®, or similar
- Bypasses phase separation and precipitation procedures
- RNA is eluted into as little as 10 µl DNase/RNase-free water. DNase I included for DNA-free RNA
- The RNA binding capacity of the Zymo-Spin I-96 Plate is 10 µg/well
- A260/A280 > 1.8, A260/A230 > 1.8. Complete removal of DNA can be performed with DNase I digestion
- TRI Reagent® provided only with cat# 11-330HT and 11-331HT
The Direct-zol-96 RNA provides a streamlined method for the purification of up to 10 µg (per well) of high-quality RNA directly from samples in TRI Reagent®. 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.) using this product. The extraction method inactivates viruses and other infectious agents. The procedure is easy: simply apply a sample in TRI Reagent® to the Zymo-Spin I96 Plate, then spin, wash, and elute the RNA. No phase separation, precipitation, or post-purification steps are necessary. The result is broad range purification of small and large RNAs suitable for subsequent RNA-based methods including RT-PCR, transcription profiling, hybridization, etc.
Sample sources: Cells from culture, solid tissue, plasma, serum, whole blood, and in vitro processed RNA (e.g., transcription products, DNase-treated or labeled RNA) or samples stored and preserved in TRI Reagent®, TRIzol®, RNAzol®, QIAzol®, TriPure, TriSure and all other acid-guanidinium-phenol reagents.
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