R2104,   Direct-zol-96 MagBead RNA (8x96 preps)  [Includes E1009 DNase I Set (250 U) w/ 10X Reaction Buffer (1 ml) x 16 – packaged separately]

R2104, Direct-zol-96 MagBead RNA (8x96 preps) [Includes E1009 DNase I Set (250 U) w/ 10X Reaction Buffer (1 ml) x 16 – packaged separately]

R2105, Direct-zol-96 MagBead RNA (8x96 preps) w/ TRI Reagent [Includes E1009 DNase I Set (250 U) w/ 10X Reaction Buffer (1 ml) x 16 & R2050-1-200 x 4– packaged separately]

13.833,75 RON
  • Quick purification of high-quality (DNA-free) total RNA directly from TRIzol®, TRI Reagent® and 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_R2105

The Direct-zol™ RNA Kits provide a streamlined method for the purification of up to 100 µg (per prep) 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 (see below).

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.).

The entire procedure typically takes only 7 minutes.

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Price 11.625,00 RON (preturile sunt fara TVA)
Description

The Direct-zol™ RNA Kits provide a streamlined method for the purification of up to 100 µg (per prep) 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 (see below).

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.).

The entire procedure typically takes only 7 minutes.

Manufacturer Zymo Research