To order chemicals, medical devices, or other restricted products please provide ID that includes your business name & shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of ID are:
- • State issued document with your organization's Federal Tax ID Number
- • State issued document with your organization's Resale Tax ID Number
- • City or County issued Business License
- • State Department of Health Services License
- • Any other ID issued by the State that includes the business name & address
* ATTN: California Customers may require additional documentation as part of the CA Health & Safety Code. Products that fall under this regulation will be placed on a mandatory 21-day hold after documentation is received. VWR will not lift restrictions for residential shipping addresses.
Specifications
- Method / Format:Column (silica-based)
- Prep size:Micro
- Refine target molecule:Total RNA
- Sample type:BloodBiofluids (serum, plasma, saliva)Cultured cellsHuman/animal cells and tissues
- Target molecule:RNA
- Description:Direct-zol™ RNA Microprep Kit
- Size:50 Preps
- Sample size:≤1×106 Cells
- Description:Direct-zol™ RNA Microprep Kit
- Sample capacity:10 µg
- Cat. no.:76020-456
Specifications
About this item
RNA from TRIzol® in seven minutes.
- Extract RNA from any sample (cells, tissues, blood, biological liquids, etc.)
- Easy Handling: No phase separation or precipitation steps
- NGS-ready: Ultra-pure RNA without phenol carryover, no DNA contamination (DNase I included)
- Total RNA Recovery: All RNA >17 nt is recovered
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 to 200 nt), is effectively isolated from a variety of sample sources (cells, tissues, serum, plasma, blood, biological liquids, etc.).
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 and more).