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![R2100, Direct-zol-96 MagBead RNA (2x96 preps) [Includes E1009 DNase I Set (250 U) w/ 10X Reaction Buffer (1 ml) x 4 -packaged separately]](https://biozyme.ro/media/catalog/product/placeholder/stores/1/NO_IMAGE_BIOZYME_1.jpg)
R2100-1-5, Direct-zol Binding Buffer Concentrate (5 ml)
238,00 RON
High-throughput, magnetic bead-based purification of high-quality (DNA-free) total RNA directly from TRIzol®, TRI Reagent® and all other acid-guanidinium-phenol based reagents (RNAzol®, QIAzol®, TriPure™, TriSure™, etc.). Bypasses phase separation and precipitation procedures, for non-biased recovery of miRNA.
SKU
ZR_R2100-1-5
The Direct-zol-96 MagBead RNA provides a high-throughput, magnetic bead based purification of high-quality RNA directly from samples in TRI Reagent and similar. The extraction method inactivates viruses and other infectious agents. Total RNA including small and non-coding 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 procedure is easy: simply add Direct-zol Binding Buffer and MagBinding Beads to a sample in TRI Reagent, 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.
| Price | 200,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
The Direct-zol-96 MagBead RNA provides a high-throughput, magnetic bead based purification of high-quality RNA directly from samples in TRI Reagent and similar. The extraction method inactivates viruses and other infectious agents. Total RNA including small and non-coding 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 procedure is easy: simply add Direct-zol Binding Buffer and MagBinding Beads to a sample in TRI Reagent, 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. |
| Manufacturer | Zymo Research |
