Shop All RNA Preparation and Purification

PureLink™ RNA Mini Kit Invitrogen™

The PureLink RNA Mini Kit is a column-based kit used to isolate high-quality total RNA from a wide variety of sample types in 20 minutes using standard laboratory equipment. The kit includes RNase-free lysis and wash solutions that protect RNA from RNases while liberating the RNA from DNA, proteins, and other cellular debris. The fast spin-column workflow is ideal for processing low to mid-throughput batch sizes. The advanced PureLink RNA Mini spin column design allows for maximum sample input (200 mg of tissue) and RNA recovery (up to 1000 µg). This means that users can process both small and large sample sizes with the same RNA isolation kit.

• Process sample inputs from 5–200 mg of animal/plant tissue or from 0.5 x 106 to 108 tissue culture cells with one spin column in 20 minutes
• Isolate more RNA than competitor mini spin columns: up to 1000 µg of total RNA from one column
• Use isolated RNA in most applications without the need for further DNase treatment (very low minimal residual DNA carry over)
• Flexible–optional on-column or post-isolation DNase treatment is available with PureLink DNase Set for easy removal of residual DNA

Extra-large binding capacity enables rapid RNA purification using standard laboratory equipment
The PureLink RNA Mini Kit provides rapid purification of total RNA from a wide range of cells and tissue types to yield up to 1000 µg of purified RNA from a single extraction (see Figure 1). High-quality total RNA can be obtained from mini- to midi-prep amounts of starting material with just trace amounts of residual genomic DNA contamination. The extra-large binding capacity enables one kit to handle most RNA isolation needs in a quick 20 minute protocol without the need for special sample processing instruments.

Easy, optional, on-column DNase treatment for sensitive applications
The PureLink RNA Mini Kit columns are highly efficient for isolating high quality total RNA while removing the majority of genomic DNA. In general, most applications requiring RNA from animal tissue or mammalian cell lines do not require additional DNase treatment. However, some applications such as gene expression analysis by qRT-PCR without intron-spanning primers or working with samples from organisms with very small or no introns may require more complete removal of residual contaminating DNA. The PureLink DNase Set allows for convenient on-column digestion of DNA during the RNA isolation protocol. Treating with DNase while “on-column” is easier and allows higher RNA recovery than treating with DNase after the RNA has been isolated. The PureLink DNase Set can also be used to remove residual DNA from RNA that has been previously purified. Both the “on-column” and post-RNA purification workflows are options available with the PureLink DNase Set.

Simplified, non-toxic RNA purification
The PureLink RNA Mini Kit utilizes non-toxic guanidine-isothiocyanate lysis buffer to protect the RNA during the isolation steps. Special RNase-free reagents combined with certified RNase-free silica membranes in a unique column configuration allow for a safe and easy procedure that can typically be completed in less than 20 minutes without the need of hazardous phenol/chloroform extraction, CsCl centrifugation, or LiCl or alcohol precipitation.

The PureLink RNA Mini Kit is recommended for use with the Homogenizer (Cat. No. 12183026), designed to homogenize cell or tissue lysates via centrifugation, prior to nucleic acid purification. The Homogenizer is especially effective for clarifying particulates from plant tissues.

For plant tissues rich in polyphenolics or starch (e.g., pine needles, potato tubers), we recommend using PureLink Plant RNA Reagent (Cat. No. 12322012) together with the PureLink RNA Mini Kit.

RiboMinus™ Plant Kit for RNA-Seq Invitrogen™

RiboMinus™ Plant Kit for RNA-Seq is the complete solution for transcriptome isolation and enrichment of the true whole transcriptome through selective depletion of ribosomal RNA in plant species. This kit offers additional plastid depletion probes designed to target chloroplast rRNA not offered in the RiboMinus™ Eukaryote Kit for RNA-Seq critical for enhanced depletion of ribosomal RNA in plants. The RiboMinus™ Plant Kit for RNA-Seq contains all the components necessary to deplete ribosomal RNA from plant species. This improvement allows for up to 99.8% depletion of the major rRNA peaks in many plant species. The RiboMinus™ Plant Kit for RNA-Seq is recommended for wheat, maize, rice, barley, soybean, sugar cane, sorghum, potato, cassava, Arabidopsis, tomato, tobacco, poplar, legume, and moss. Additional plant species can be bioinformatically assessed by contacting Invitrogen.

Working with something other than human, mouse, or plant? Contact us with your species and sequence. Simply include your FASTA sequence in *.txt file format for the ribosomal sequences you would like to verify, with the subject line titled 'RiboMinus for (your organism here)', and we'll work with you to find the right probe for your RiboMinus® rRNA depletion.

Homogenizer Invitrogen™

The Homogenizer is for use with the Ambion™ PureLink™ RNA Mini Kit (Cat. Nos. 12183020, 12183018A, 12183025) to reduce the viscosity of difficult tissue samples between 5 and 30 mg during RNA isolation.

GeneJET RNA Cleanup and Concentration Micro Kit Thermo Scientific™

Thermo Scientific GeneJET RNA Cleanup and Concentration Micro Kit is designed for rapid and efficient concentration of prepurified RNA samples, as well as for RNA cleanup after DNase I treatment and other enzymatic reactions.

The kit combines the convenience of spin column technology with the selective binding properties of a silica membrane, eliminating the need for tedious resin manipulations or toxic phenol-chloroform extractions.


• Advanced column design—easy to open, load and handle.
• Elute in 6 to 10 µL volume.
• 85 to 100% recovery of a high integrity RNA.
• Fast and simple—procedure takes less than 5 minutes.

• The purified RNA can be used in common downstream applications
• RT-PCR, RT-qPCR, Northern blotting and other RNA-based analysis

Ion Total RNA-Seq Kit v2 Ion Torrent™

The Ion Total RNA-Seq Kit v2 includes the reagents needed to prepare representative cDNA libraries for strand-specific RNA sequencing on the Ion GeneStudio™ S5, Ion Proton™, or the Ion Personal Genome Machine™ (PGM™) systems. The Ion GeneStudio S5 and Ion Proton systems are ideally suited for sequencing the whole transcriptome (ribosomal RNA depleted or polyA), while the Ion GeneStudio S5 and Ion PGM systems are suitable for small RNA, as well as viral and bacterial transcriptomes. Either small RNA (such as microRNA) or whole transcriptome RNA samples can be prepared for next-generation sequencing using the Ion Total RNA-Seq Kit v2. Version 2 of the Ion Total RNA-Seq Kit is an improvement over the first generation kit. The gel size selection step in the small RNA workflow has been replaced with a magnetic bead-based method. Magnetic bead-based purification replaces all of the filter cleanup steps and the total reaction time has been reduced to 6 hours.

Additional Features of the New Ion Total RNA-Seq Kit v2:

• Greater accuracy—SuperScript® VILO™ and Platinum® PCR SuperMix High Fidelity added for highest template fidelity
• Barcode compatible—works with Ion Xpress™ RNA-Seq Barcode 01-16 Kit for multiplexing
• Automation friendly—magnetic bead-based purification simplifies automation of library construction

As with the previous kit, the Ion Total RNA-Seq Kit v2:

• Preserves strand information—all mapped reads are aligned in the direction of transcription relative to the chromosomal strand
• Allows you to choose your workflow—interrogate either small RNA or the whole transcriptome
• Allows you to analyze any type of RNA—supports small RNA, rRNA depleted total RNA, and poly(A) RNA

The Ion Total RNA-Seq Kit v2 is designed to make cDNA library preparation for the Ion Proton™ and PGM™ systems fast and flexible. It can be used to generate a representative cDNA library, flanked by specific sequences necessary for sequencing, from any type of RNA sample.

Designed as a complete solution with a common workflow, the Ion Total RNA-Seq Kit v2 combines optimized reagents and protocols for discovery of small RNAs and isoforms, coding RNA, noncoding RNA, and alternative splice variants.

Small RNA Analysis
During small RNA library construction, the 3' and 5' adaptors are attached directionally and simultaneously. As a by-product of this step, an adaptor:adaptor product may be formed without an RNA insert. This byproduct will amplify during first strand synthesis and PCR. If not removed, > 50% of the reads will be the adaptor dimer. Historically, the only way to separate the adaptor dimer from the wanted small RNA containing library fragments has been through gel size selection. The Ion Total RNA-Seq Kit v2 uses proprietary technology to inhibit cDNA synthesis of the adaptor byproduct, thus allowing cDNA separation with magnetic bead-based technologies. Total reaction time has been reduced from 1.5 days to approximately 6 hours. A separate Magnetic Bead Cleanup Module is included with the kit. Additional modules may be purchased separately.

Start with total RNA containing as little as 5–100 ng of miRNA, or RNA enriched for small RNA containing 1–100 ng of miRNA. The small RNA protocol provides guidance on whether to start with total RNA or RNA enriched for small RNA, based on the small RNA content of your sample. Small RNA enrichment protocols are also provided.

Whole Transcriptome Analysis
The whole transcriptome protocol enables construction of strand-specific libraries in approximately 5 hours. Starting with as little as 100 ng of total RNA, construct a library from 1 ng of poly(A) RNA or 25 ng of rRNA-depleted RNA following the RNA enrichment and library generation protocols provided in the manual. Because the libraries are not limited to cDNA derived only from poly(A) RNA, Ion Total RNA-Seq Kit libraries support a more thorough investigation of transcriptome complexity, capable of characterizing known and undocumented transcripts, including alternative splice variants, fusion transcripts, and SNPs.

Preserve Strand Information
Unlike methods that ligate adapters to double-stranded cDNA, the Ion Total RNA-Seq Kit v2 utilizes proprietary Ambion® technology to attach the adapters in a directional manner that preserves strand information in the resulting libraries. In addition, both the 3' and 5' adapters are attached simultaneously, reducing ligation and clean-up steps.

Preserving strand orientation during library construction helps enable more accurate determination of the structure and expression level of transcripts, and can aid in the discovery of novel transcription regions from both the positive and negative genomic strands.

The Ion Total RNA-Seq Kit v2 is designed to create RNA libraries from up to 48 samples for small RNA or whole transcriptome sequencing on the Ion Proton™ or PGM™ systems.

RNAlater™ Stabilization Solution with Manual Invitrogen™

RNAlater® RNA Stabilization Solution stabilizes and protects cellular RNA in intact, unfrozen tissue samples, eliminating the need to immediately process tissue samples or to freeze samples in liquid nitrogen for later processing. Tissue pieces can be harvested and submerged in RNAlater® RNA Stabilization Solution for storage without jeopardizing the quality or quantity of RNA obtained after subsequent RNA isolation. Advantages of using RNAlater® RNA Stabilization Solution:

Effectiveness—stabilize RNA for 1 day at 37°C, 1 week at 25°C, 1 month at 4°C, or indefinitely at -20°C
Simplicity—a single reagent that immediately inactivates RNases and stabilizes RNA within tissues or cells
Convenience—no need to freeze samples in liquid nitrogen or rush samples back to the lab freezer
Mobility—perfect for tissue collection 'in the field'
Versatility—compatible with many RNA isolation procedures, including most RNA isolation kits

RNAlater® RNA Stabilization Solution has been tested on a variety of mammalian tissues, plants, E. coli, Xenopus, fish, and Drosophila. It is ideal for:

• Protecting RNA integrity in tissues rich in RNases
• Collecting samples from different time points without having to process the samples from each time point immediately
• Archiving tissues for future microdissection
• Submerging animal cavities or organs to stabilize RNA during lengthy dissection procedures
• Collecting samples at locations (e.g., hospitals, field sites, the space shuttle) where immediate RNA isolation is not possible
• Shipping samples on wet ice or even at room temperature if shipped overnight

RNAlater® RNA Stabilization Solution procedure
The dissected tissue (less than 0.5 cm in any one dimension) is simply submerged in approximately 5 volumes of RNAlater® solution at room temperature. The solution permeates the cells, stabilizing the RNA. The sample can then be stored indefinitely at -20°C (the tissue does not freeze), at 4°C for up to a month, or at 25°C for up to a week. For RNA isolation, the tissue is simply removed from RNAlater® solution and treated as though it had just been harvested. Most tissues can be transferred directly to a lysis buffer and homogenized. Samples treated with RNAlater® solution and then frozen can be ground with mortar and pestle or thawed and processed like fresh tissue without concern for cell rupture and release of RNases since the RNases have already been inactivated. Cells can be spun out and then added to lysis buffer, or in some cases, RNAlater® solution can be added along with the cells directly to the lysis buffer.

Compatible with a variety of procedures
RNAlater® RNA Stabilization Solution is compatible with one-step RNA isolation methods, such as TRIzol® Reagent; with glass binding methods such as Qiagen's RNeasy™ or the Ambion® RNAqueous® kit; with acid phenol extraction methods such as the Ambion® ToTALLY RNA™ kit; and with methods that use oligo(dT) selection of mRNA, such as the Ambion® Poly(A)Purist™ kit. In-house research, as well recently published independent research, indicates that the use of RNAlater® RNA Stabilization Solution for tissue storage does not affect the outcome of subsequent RNA expression analysis experiments compared to other processing methods.

TRIzol™ Plus RNA Purification Kit Invitrogen™

The TRIzol® Plus RNA Purification Kit provides a simple, reliable, and rapid method for isolating high-quality total RNA from a wide variety of samples, including animal and plant cells, tissue, bacteria, and yeast. The kit combines the strong lysis capability of TRIzol® Reagent, followed by a convenient and time-saving silica-cartridge purification protocol from the PureLink® RNA Mini Kit, to provide ultrapure total RNA typically within an hour, even from difficult samples such as fibrous or fatty tissues.

Features of this kit include:

• Combined TRIzol®-based lysis and PureLink™ spin column-based RNA isolation technologies
• Superior lysis capability and convenient protocol

Two products in one
The TRIzol® Plus RNA Purification System couples the lysis capabilities of TRIzol® Reagent with the 1000 µg column-;binding capacity of the PureLink™ RNA Mini Kit, resulting in high RNA integrity and yield. The TRIzol® Plus RNA Purification System includes protocols for a variety of sample types, including fibrous or fatty tissues and plant material. The combination of TRIzol® Reagent followed by silica-cartridge purification of RNA is the recommended RNA purification method in the gene expression industry. The TRIzol® Plus RNA Purification Kit provides the reagents and an optimized protocol to purify total RNA for gene expression studies using an industry recommended method.

Simple lysis to column purification protocol
TRIzol® Reagent sample lysis maintains the integrity of the RNA, while disrupting cells and dissolving cell components. TRIzol® Reagent also provides an immediate and highly effective inhibition of RNase activity during sample homogenization. Following lysis, RNA in the lysed sample is bound to the clear silica-based membrane in the PureLink™ RNA Mini Kit Spin Cartridge, washed to remove contaminants, and then eluted in RNase-Free water (Tris Buffer, pH 7.5 may also be used).

RiboMinus™ Concentration Module Invitrogen™

The RiboMinus Concentration Module is used to concentrate RiboMinus RNA while retaining species of <200 nucleotides (nt) for further use in downstream applications.

Generally, RNA species of <200 nt are excluded from silica spin columns under standard binding conditions for RNA isolation. Studies have shown the importance of these small RNA species, which include regulatory RNA molecules such as microRNA (miRNA), short interfering RNA (siRNA), and snRNA. To retain RNA of <200 nt during the concentration step of RiboMinus RNA isolation, the RiboMinus Concentration Module is used with a modified silica spin column protocol (binding of RNA is performed with 60% ethanol).

The binding conditions of the spin column protocol are optimized for the RiboMinus RNA sample with ethanol and buffer. The sample is loaded onto a spin column. The RiboMinus RNA binds to the silica-based membrane in the column and impurities are removed by thorough washing with Wash Buffer. The RiboMinus RNA is then eluted in RNase-free water.

GeneJET RNA Purification Kit Thermo Scientific™

Thermo Scientific GeneJET RNA Purification Kit is a simple and efficient system for purification of total RNA from mammalian cultured cells, tissue, human blood cells, bacteria, and yeast.

The kit utilizes a silica-based membrane technology in the form of a convenient spin column, eliminating the need for tedious cesium chloride gradients, alcohol precipitation, or toxic phenol-chloroform extractions.

RNA molecules longer than 200 nucleotides can be isolated with the GeneJET RNA Purification Kit in 15 minutes after the lysis step. The high-quality purified RNA can be used in a wide range of downstream applications, including RT-PCR, RT-qPCR, Northern blotting, and other RNA-based analyses.


Universal – can be used for both cell and tissue samples from a wide range of sources: mammalian blood, mammalian cell cultures, mammalian tissues, insect, yeast, and bacteria
Efficient – high yields of total RNA.
Fast – 15 minutes after lysis step
Pure – an A260/280 ratio > 1.9
Convenient – spin columns are capped and assembled with collection tubes


• Fast extraction of high purity RNA suitable for all conventional molecular biology procedures, including:
• Northern blotting
• Nuclease protection assayIncludes Proteinase K Lysis Buffer Wash Buffer 1 (concentrated) Wash Buffer 2 (concentrated) Water, nuclease-free GeneJET RNA Purification Columns (pre-assembled with Collection Tubes) Collection Tubes (2 ml) Collection Tubes (1.5 ml) Detailed Protocol

Total RNA Lysis Solution, Nucleic Acid Purification Invitrogen™

Total RNA Lysis Solution is a 2X concentrate ideal for the chemical disruption of cells and tissue (cultured cells, primary cell isolates, and animal/plant tissues) prior to RNA or DNA extraction. Following downstream purification (e.g. using the 6100 PrepStation), intact RNA can be isolated that is free of contaminating protein and metal ions. Total RNA Lysis solution is the recommended reagent for the Total RNA Isolation Chemistry System for the ABI PRISM™ 6100 Nucleic Acid PrepStation.

For research use only. Not for use in diagnostic procedures.

PureLink™ Plant RNA Reagent Invitrogen™

Plant RNA Reagent is a single-component solution optimized for the isolation of high yields of high-quality total RNA from a variety of plant tissues, especially those rich in polyphenolics (e.g., conifer needles) or starch (e.g., potato tuber or seeds). Features of the Plant RNA Reagent:

• Isolate high-quality RNA from difficult plant materials
• Use for small-scale and large-scale RNA isolations

Improved quality and purity of plant RNA
Plant RNA Reagent is optimized to have less sample DNA contamination, to be twice as effective as TRIzol® Reagent, and have a simplified RNA extraction protocol for minimized time and labor. The end result is high-yield, high-purity RNA (determined by A260/A280 and gel analysis) from a variety of plant material sources.

Works for milligram to gram quantities of starting material
Plant RNA Reagent provides greater flexibility for sample size and processing formats, and can be used for both small-scale (up to 0.1 g plant tissue) and large-scale (0.1–5 g plant tissue) total RNA isolation. The amount supplied (100 mL) is sufficient for 200 reactions using 100 mg of tissue, or 4 reactions using 5 g of tissue.

Isolated RNA is ideal for a variety of applications and products:

cDNA library construction kits
Real-Time PCR (qPCR)
Northern blotting kits & reagents
Poly(A) selection kit
RNase control reagents & assays

Cells-to-cDNA™ II Kit Invitrogen™

The Ambion® Cells-to-cDNA™ II Kit (patent pending) produces cDNA from cultured mammalian cells in less than 2 hr. No RNA isolation is required. This kit contains sufficient reagents for 100 reactions and is ideal for those who want to perform reverse transcription reactions on small numbers of cells, numerous cell samples, or for scientists who are unfamiliar with RNA isolation.

• No RNA purification required
• From cells in culture to cDNA in less than 2 hr
• Detect rare messages in as few as 1 cell
• Ideal for labs not equipped for RNA isolation

Ideal for RT-PCR Applications
The Cells-to-cDNA™ II Kit (patent pending) integrates RNase inactivation and DNase I treatment into an RT-PCR compatible cell lysis buffer, eliminating RNA isolation altogether. Most cell lysis buffers contain strong denaturants that if carried over into enzymatic reactions would inhibit or inactivate most enzymes. If a lysis buffer without strong denaturants is used, endogenous RNase can quickly degrade cellular RNA. The Cells-to-cDNA™ II Kit contains a novel Cell Lysis Buffer that inactivates endogenous RNases without compromising downstream enzymatic reactions. After inactivation of RNases, the cell lysate can be directly added to a cDNA synthesis reaction. Cells-to-cDNA™ II is compatible with both one-step and two-step RT-PCR protocols.

Quantitative—Linear Results and No Detectable DNA Contamination
To illustrate the quantitative, linear response of Cells-to-cDNA™ II to variations in input cell number, a real-time quantitative RT-PCR experiment was performed using the ABI 7700 Sequence Detection System. Plotting cycle threshold (Ct) versus cell concentration for GAPDH yielded a standard curve with a correlation of 0.99. Thus, Cells-to-cDNA™ II yields linear results for 1 to 10,000 cells/ µL in a real-time RT-PCR two-step assay. It should also be noted that the minus-template PCR control for the GAPDH experiment was negative, indicating complete removal of genomic DNA.

Simple Procedure
The kit comes with everything you need to go from cultured cells to PCR-ready cDNA in less than 2 hr; no RNA isolation is required. Cells are first washed with PBS and then resuspended in the Cell Lysis Buffer. A brief heating simultaneously lyses the cells and inactivates RNases. An optional DNase digestion is then performed to degrade genomic DNA, followed by a heat inactivation step. A fraction of the cell lysate is then used in a reverse transcription reaction with the included reagents.

Accessory Products:
SuperTaq™ Thermostable Taq DNA Polymerase is recommended and available separately (SKU#s AM2050 and AM2052). For optimal amplification of fragments greater than 1 kb, use SuperTaq™ Plus Thermostable Taq DNA Polymerase (SKU#s AM2054 and AM2056).

Fast SYBR™ Green Cells-to-CT™ Kit Invitrogen™

Ambion® Fast SYBR® Green Cells-to-CT™ Kit is a fast, easy, and robust method to go directly from cultured cells to real-time PCR results. A breakthrough cell lysis and RNA stabilization technology eliminates the laborious and time-consuming RNA purification process completely. The kit includes sufficient reagents for 400 reactions. The Fast SYBR® Green Cells-to-CT™ Kit contains AmpliTaq® Fast DNA Polymerase, UP, which allows instant hot start, thus minimizing non-specific product formation with fast real-time PCR.

• Includes optimized reagents to work efficiently, right out of the box
• Simple, effective Cells-to-CT™ technology enables sample preparation at room temperature in only 7 minutes, including DNase treatment
• Validated accuracy, exceptional reproducibility, and maximal sensitivity from 10 to 100,000 cells per sample; results equivalent to those from purified RNA

Extraordinary Value
The kit includes reagents for sample preparation integrated into a complete, optimized gene expression workflow including reverse transcription reagents and a high-performance PCR master mix with SYBR® Green.

Extraordinary Ease
The protocol begins with a simple 7-minute sample preparation procedure. First, cells are washed in PBS, and then lysed for 5 minutes at room temperature; DNase treatment can be performed concurrently. The lysis reaction is stopped, and the sample is then ready for reverse transcription or storage at –20°C for up to 5 months. Because samples are processed directly in culture plates (96- or 384-well), sample handling and the potential for sample loss or transfer error are minimized, resulting in higher reproducibility. Following sample preparation, a portion of the cell lysate is added to an RT reaction followed by real-time PCR using the included master mix.

Extraordinary Performance
To demonstrate the performance of the kit, replicate experiments were run using either traditional RNA purification and real-time PCR analysis, or the FastSYBR® Green Cells-to-CT™ Kit. The kit shows equivalent performance to results obtained using purified RNA for analysis of 10 to 100,000 cells. In addition, the sensitivity, efficiency, and dynamic range were shown to be superior to competitor lysate kits. Samples prepared with the kit have been tested for compatibility on various real-time PCR platforms, including those from Applied Biosystems®, Roche, and Bio-Rad.

Accessory Product:
The SYBR® Green Cells-to-CT™ Control Kit (SKU# 4402959) contains a Xeno™ RNA control and primer set and is recommended to monitor the efficiency of cell lysis and amplification inhibition in Cells-to-CT™ reactions.

GeneJET NGS Cleanup Kit Thermo Scientific™

Thermo Scientific GeneJET NGS Cleanup Kit provides protocols optimized specially for fast DNA fragment cleanup or adapter removal procedures. The clean up protocol results in higher than 70% recovery of DNA fragments larger than 150 bp and more than 97% removal of adapters. Adapter removal protocol results in more than 70% recovery of DNA fragments larger than 200 bp and more than 99% removal of adapters. The entire procedure takes 5 minutes for DNA fragment library cleanup from enzymatic reaction mixtures and 7 minutes for adapter removal protocol. Spin columns technology in combination with unique binding buffer allows to get the reproducible yields of DNA fragments in the wide starting material range (5 ng - 1 µg of DNA fragments).

The GeneJET NGS Cleanup Kit is compatible with Illumina™, Life Technologies library preparation workflows.


Fast—high quality DNA fragments obtained within 5 min
Robust—reliable cleanup and size selection from different reaction mixtures and buffers, such as end-conversion, ligation, adapter addition, PCR mixtures, fragmentation buffers
Efficient—DNA recovery up to 90%
NGS-grade purity—free of primers, adapters, nucleotides, enzymes and other reaction components inhibiting NGS workflow.


• Purified DNA fragments are ideal for use in:
• PCR and qPCR
• Next Generation Sequencing workflow

• Binding Buffer (R2811)
• Prewash Buffer (conc.) (R2821)
• Wash Buffer (conc.)(R2831)
• Elution Buffer (10 mM Tris-HCl, pH 8.5)
• DNA Purification Micro Column & Collection Tube
• Collection Tube

Related Products
Binding Buffer for GeneJET NGS Cleanup Kit
Prewash Buffer for GeneJET NGS Cleanup Kit
Wash Buffer for GeneJET NGS Cleanup Kit
GeneJET Plasmid Miniprep Kit

Plant RNA Lysis Solution Thermo Scientific™

Thermo Scientific GeneJET Plant RNA Lysis Solution is a component of the GeneJET Plant RNA Purification Mini Kit (K0801/K0802) and may be purchased separately. Provided in 200 mL aliquots.
Results per page