RNA Preparation and Purification
Molecular Research Center TRI REAGENT LS 200 ML
For single-step isolation of total RNA or simultaneous isolation of RNA, DNA and proteins from liquid samples. 0.75 ml of TRI Reagent LS processes 0.25 ml of liquid samples.
Apexbio Technology LLC SP6 H.Y RNA SYNTHESIS KIT 25R
SP6 H.Y RNA SYNTHESIS KIT 25R APEXBIO TECHNOLOGIES
Zyagen Labs Mouse C57 spinal cord RNA is a high pure intact total RNA isolated from freshly harvested normal healthy C57BL/6 Mouse SPINAL CORD tissues, treated with DNase and dissolved in water. RNA is ready for immediate use in any downstream application.
Zyagen Total RNA is routinely extracted from freshly harvested normal healthy tissues of single donor using classical guanidine isothiocyanate–phenol:chloroform extraction method which allows the rapid isolation of total RNA including microRNAs. RNA is treated with RNase-free DNase to remove residual DNA, precisely quantified, and stored at -80oC. The integrity of each RNA sample as indicated by intact ribosomal RNA is verified by denatured agarose gel electrophoresis. The purity of RNA is assessed by NanoDrop (A260/A280: 1.9-2.1). Residual DNA contamination is tested by PCR. RNA is ideal for Northern blotting, ribonuclease protection assay, SI nuclease assay, RT-PCR/Q-PCR/RACE analysis, cDNA synthesis, RNA differential display, microRNA studies, and purification of mRNA for library construction. Total RNA sample is provided in RNase-free water at a concentration of 1 mg/ml and shipped on dry ice.
Revvity Health Sciences Inc AlphaLISA SureFire Ultra Human Total ATM Detection Kit, 500 Assay Points
AlphaLISA SureFire Ultra Human Total ATM Detection Kit, 500 Assay Points
Zyagen Labs Mouse C57 thymus total RNA is a high pure intact total RNA isolated from freshly harvested normal healthy C57BL/6 Mouse THYMUS tissues, treated with DNase and dissolved in water. RNA is ready for immediate use in any downstream application.
Zyagen Total RNA is routinely extracted from freshly harvested normal healthy tissues of single donor using classical guanidine isothiocyanate–phenol:chloroform extraction method which allows the rapid isolation of total RNA including microRNAs. RNA is treated with RNase-free DNase to remove residual DNA, precisely quantified, and stored at -80oC. The integrity of each RNA sample as indicated by intact ribosomal RNA is verified by denatured agarose gel electrophoresis. The purity of RNA is assessed by NanoDrop (A260/A280: 1.9-2.1). Residual DNA contamination is tested by PCR. RNA is ideal for Northern blotting, ribonuclease protection assay, SI nuclease assay, RT-PCR/Q-PCR/RACE analysis, cDNA synthesis, RNA differential display, microRNA studies, and purification of mRNA for library construction. Total RNA sample is provided in RNase-free water at a concentration of 1 mg/ml and shipped on dry ice.
Macherey-Nagel NucleoSpin RNA Columns, 250 columns
NucleoSpin RNA Columns (250) binding columns for the isolation of RNA pack of 250
Macherey-Nagel NucleoSpin RNA Columns, 50 columns
NucleoSpin RNA Columns (50) binding columns for the isolation of RNA pack of 50
American Research Products Inc PLANT FLAVONOIDS COLORIMETRIC
5000265545 PLANT FLAVONOIDS COLORIMETRIC
Macherey-Nagel NucleoSpin RNA Clean-up XS, 10 preps
NucleoSpin RNA Clean-up XS (10) 10 preps for the clean-up of total RNA - NucleoSpin RNA XS Columns, Collection Tubes, buffers
New England Biolabs, Inc. NEBNext Ultra™ II RNA Library Prep with Sample Purification Beads – 24 reactions
The Ultra II RNA Library Prep Kit for Illumina is designed for non-directional (non-strand-specific) RNA library construction, and delivers significantly increased sensitivity and specificity from your RNA-seq experiments, from ever-decreasing amounts of input RNA. In conjunction with ribosomal RNA (rRNA) depletion or poly(A) mRNA enrichment, the kit enables the production of high quality libraries from 5 ng or 10 ng of Total RNA, respectively, up to 1µg. For convenience, this kit includes SPRISelect beads.
New England Biolabs, Inc. NEBNext® Ultra™ II RNA Library Prep Kit for Illumina® – 24 reactions
The Ultra II RNA Library Prep Kit for Illumina is designed for non-directional (non-strand-specific) RNA library construction, and delivers significantly increased sensitivity and specificity from your RNA-seq experiments, from ever-decreasing amounts of input RNA. In conjunction with ribosomal RNA (rRNA) depletion or poly(A) mRNA enrichment, the kit enables the production of high quality libraries from 5 ng or 10 ng of Total RNA, respectively, up to 1µg.
- Generate the highest yields of high quality libraries, with a broad range of input amounts
- Increase the complexity and transcript coverage of your libraries
- Optimize your time with streamlined workflows, reduced hands-on time, and automation compatibility
- Rely on robust performance, even with low quality RNA, including FFPE
Norgen Biotek Corp Plant/Fungi Rna Purif. Kit
Norgen’s Plant/Fungi Total RNA Purification Kit provides a rapid method for the isolation and purification of total RNA, including virus and viroid RNA, from a wide range of plants. Total RNA can be purified from fresh or frozen plant tissues, plant cells or filamentous fungi samples using this kit. All sizes of RNA are purified, including microRNA (miRNA) . The procedure is rapid and convenient. The RNA is purified without the use of phenol or chloroform. The purified RNA is of the highest quality, and can be used in a number of downstream applications including real time PCR, reverse transcription PCR, Northern blotting, RNase protection and primer extension, and expression array assays. Norgen's Plant/Fungi Total RNA Purification Kit is also available in a 96-well format for high throughput applications. Purification with the 96-well plates can be performed using either a vacuum manifold or centrifugation.
Biochain Institute Inc Total RNA - Human Adult Normal Tissue: Tongue, 50 ug/PK
BioChain's Total RNAs are isolated from a wide variety of documented human normal, diseased, and tumor tissues, mouse, rat, monkey, and plant tissues. Total RNA isolation is performed using proprietary techniques. Contamination by RNase, genomic DNA polysaccharides, and proteoglycans has been effectively eliminated. The integrity of the total RNAs is assured by checking for a ratio of greater than 1:1 between 28s and 18s ribosomal RNA. High efficiency reverse transcription using the Total RNA is demonstrated.