For research use only and NOT intended for in vitro diagnostics.
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These kits are suitable for the isolation of total RNA from a range of samples including cells, bacteria, yeast, virus and bodily fluids including plasma/serum, blood, saliva, CSF and more. Extract high quality and purity RNA with excellent RIN values and A260/A280 suitable for downstream applications including qRT-PCR, RT-PCR, microarrays, NGS and more. These kits purify all sizes of RNA from large mRNA, lncRNA down to microRNA (miRNA) in the same fraction without the requirement of phenol. Isolate all RNA sequences at an equal rate irrespective of size. Moreover, when the RNA sequences are small (e.g. miRNA), the column binds small RNAs regardless of their GC content.
Total RNA Purification 96-Well Kit (High Throughput and High Throughput Deep Well)
This 96-well kit provides a rapid method for the high-throughput isolation and purification of total RNA in 30 minutes using vacuum manifold, plate centrifuge, or liquid handlers with vacuum capabilities. Total RNA can be isolated from a broad range of sample sources including cultured cells, tissues, blood, serum, plasma, bacteria, yeast, fungi, and viruses.
Isolate RNA after Purifying EVs and Exosomes
Ultracentrifugation, Exoquick, Filtration
| Cat. # | Name | Elution Volume | Plasma/Serum | Urine | Cell-Culture Media |
|---|---|---|---|---|---|
| 55000 | Plasma/Serum RNA Purification Mini Kit | 10 - 25 µL | 50 µL - 1 mL | 250 µL - 1 mL | 5 - 10 mL |
| 35300 | Total RNA Purification Micro Kit | 20 - 50 µL | 1 - 4 mL | 2 - 10 mL | 10 - 20 mL |
| 17200 | Total RNA Purification Kit | 50 - 100 µL | 4 - 10 mL | 11 - 30 mL | 20 - 35 mL |
Figure 1. High Quality of Isolated RNA with Complete Size Range. Unlike most competitors' kits, Norgen's Total RNA Purification Kit allows for the isolation of all sizes of RNA, from the very large RNA down to the microRNA, without the use of phenol. Total RNA was isolated from 1 x 109 E. coli cells using Norgen’s Total RNA Purification Kit and a competitor’s kit. Five microliters and 1 µL of the 50 µL isolated RNA was analyzed on an agarose gel (Panel A) and the Agilent® 2100 BioAnalyzer RNA Nano 6000 chip (Panel B), respectively. Note the presence of small RNA species (red square) in the samples isolated via Norgen's kit and the absence of these RNA species in the competitor RNA preparation.
Figure 2. Amplification of Both Large and Small RNAs in the Same Extraction. Norgen's Total RNA Purification Kit isolates the complete size range of RNA, including small RNAs without the use of phenol. Total RNA was isolated from 0.75 million HeLa cells using Norgen's Total RNA Purification Kit, various silica-based competitors and phenol-based TRI Reagent. RT-PCR was performed according to Shi and Chiang (2005). Fifteen microliters of the 50 µL isolated RNA were polyadenylated in a 50 µL Poly-(A)-Polymerase reaction. Four microliters of the polyadenylated RNA were used in a 20 µL reverse transcription reaction with a poly T adaptor primer. One microliter of the reverse transcription was used in a 20 µL qPCR reaction with primers against the human microRNAs (miR-19 and miR-21) and large mRNA (S15). Only the use of Norgen's Total RNA Purification Kit resulted in detection of both microRNAs and mRNA amplification products similar to Competitor 2's kit but without the use of phenol.
Figure 3. High Quality of RNA from a Diverse Range of Inputs. Norgen's Total RNA Purification Kit allows RNA isolation from a wide range of species or tissue types. Total RNA was isolated from 5 x 108 E. coli cells, 1 x 106 HeLa cells, 100 µL rat blood and 10 mg hamster kidney using Norgen's Total RNA Purification Kit. One microliter of the 50 µL isolated RNA was analyzed on the Agilent® 2100 BioAnalyzer using an RNA Nano 6000 chip. Note the integrity of RNA from all inputs with the presence of small RNA species. Norgen's Total RNA Purification Kit consistently isolates high quality RNA from various inputs that score a RIN value between 8 and 10.
Figure 4. Great Isolation Sensitivity. Norgen's Total RNA Purification Kit allows sensitive RNA extraction from as little as a single cell. Total RNA was extracted from a decreasing number of 293 HEK cells from 1 million cells down to a single cell. Five microliters of the 50 µL isolated RNA was then subjected to a 20 µL reverse transcription using oligo dT primer. Three microliters of the reverse transcription was used in a 20 µL PCR reaction with primers to detect the human beta-actin transcripts. PCR products of beta-actin were detected from as little as a single cell. M is the marker lane.
Figure 5. Linear and Sensitive Isolation of Both Large and Small RNA. Norgen’s Total RNA Purification Kit allows consistent isolation of both large and small RNA from different input amounts. Total RNA was isolated from 10 to 100,000 HeLa cells using Norgen's Total RNA Purification Kit (blue), a competitor’s silica-based kit (green) and a phenol-based RNA extraction method (red). Relative expression of miR-21 (Panel A), and S15 (Panel B) was determined by RT-qPCR of total RNA samples. In brief, one microliter of the 50 µL isolated RNA was then subjected to a 20 µL reverse transcription using miR-21 stem-loop reverse primer or oligo dT primer. Two microliters of the reverse transcription was used in a 20 µL real-time PCR reaction with primers to detect the human miR-21 (Panel A) and the S15transcripts (Panel B). The resulting threshold cycle (Ct) values were plotted against input cell number. RNA isolated using Norgen's Total RNA Purification had the best linearity (higher R2) and sensitivity (lower Ct) for both large RNA (S15) and small RNA (miR-21).
Figure 6. Effective and Consistent Detection of miRNA from Plasma. Norgen's Total RNA Purification Kit can effectively isolate miRNA from plasma. Total RNA was isolated from 50, 100 or 200 µL of rat plasma in triplicates using Norgen's Total RNA Purification Kit (blue), a competitor’s silica-based kit (green) and a phenol-based RNA extraction method (red). Stem loop RT-qPCR using primers specific to miR-21 was performed. In brief, two microliters of the 50 µL isolated RNA was then subjected to a 20 µL reverse transcription using miR-21 stem-loop reverse primer or oligo dT primer. Three microliters of the reverse transcription was used in a 20 µL real-time PCR reaction with primers to detect the human miR-21. Norgen's Total RNA Purification Kit is the only product that showed (1) consistent detection of miR-21 transcripts across all input volumes, and (2) Ct values correlated to input volume (decrease Ct with increase input).
Figure 7. Recovering Diverse miRNA Species from Plasma with Better Consistency. Norgen's Total RNA Purification Kit isolates plasma RNA that performs more consistently in downstream applications such as microarrays. Total RNA including miRNA was isolated from 100 µL of mouse plasma in duplicate using Norgen's Total RNA Purification Kit, Competitor 1's leading miRNA Kit or a phenol-based RNA extraction method. One hundred nanograms of extracted RNA from each kit was applied to an Illumina microRNA expression profiling kit. Scatter plots display better consistency (better clustering) of replicate signals from Norgen's samples. Genes with Pval < 0.01 for both replicates were in blue. The associated table suggested that Norgen's protocol recovered the same diversity of miRNA with better consistency (higher r2 value).
Figure 8. Better Diversity of miRNA Detected from Plasma. Norgen's Total RNA Purification Kit isolates miRNA from plasma with better diversity than a leading competitor. Total RNA including miRNA was isolated from 100 µL of plasma using Norgen's Total RNA Purification Kit or 625 µL of plasma using Competitor A's leading miRNA Kit, and was applied to an NCode expression profiling kit. Microarray images suggested that Norgen's Total RNA Purification Kit (left) isolates a better diversity of miRNA from smaller input amount of plasma than the competitor’s miRNA kit (right). Image courtesy of LC Sciences, Houston.
Figure 9. Better Diversity of miRNA Detected from HeLa Cells using Illumina Small RNA Next Gen Sequencing. Norgen's Total RNA Purification Kit isolates miRNA from HeLa cells with better diversity than a leading competitor. Total RNA including miRNA was isolated from 1 million HeLa cells using Norgen's Total RNA Purification Kit and Competitor Q's leading miRNA Kit, and was applied to Illumina Small RNA Next Gen Sequencing on a MiSeq sequencer. Panel A showed that Norgen’s Total RNA Purification Kit recovers a higher number of miRNAs than the competitor. In particular, the higher diversity is achieved with a faster and simpler procedure in as little as 20 minutes of RNA sample preparation time without the use of phenol. Panel B is a scatter plot of the average RPM (reads per million) of the miRNAs detected used to compare Norgen and the competitor's kit recovery of miRNA. Norgen's Total RNA Purification Kit recovered a significantly higher number of miRNAs that have higher RPM, as summarized in the graph insert as well as in Panel C.
Figure 10. Consistent Yield of High Quality RNA with Complete Size Range without the Use of Phenol. Norgen's Total RNA Purification 96-Well Kit allows for the consistent isolation of high quality RNA, with complete sizes ranging from very large RNA down to small RNA without the use of phenol. Total RNA was isolated from 0.5 mL aliquots of an overnight culture of E. coli (~5 x 108 cells/mL) using Norgen's Total RNA Purification 96-Well Kit in 16 replicates. Five microliters of the 75 µL isolated RNA were resolved on a 1.2% formaldehyde agarose gel. All 16 replicates showed both high yield and high quality. In addition, all replicates showed effective recovery of all sizes of RNA including the small RNA (arrow).
Figure 11. High Quality of RNA from a Diverse Range of Inputs. Norgen's Total RNA Purification 96-Well Kit allows for RNA isolation from a wide range of species and tissue types. Total RNA was isolated from 8 mg of brain (Lanes A), kidney (Lanes B), liver (Lanes C), lung (Lanes D) and spleen tissue (Lanes E), 7.5 x 105 HeLa (Lanes F) and CHO cells (Lanes G), and 5 x 108 bacteria (Lanes H) using Norgen's Total RNA Purification 96-Well Kit. Five microliters of the 75 µL isolated RNA were resolved on a 1.2% formaldehyde agarose gel. From observing the formaldehyde-agarose gel, it can be seen that Norgen's kit can be used to successfully isolate total RNA, including small RNA species, from a broad range of sample types.
Figure 12. Isolation of Both Large and Small RNA. Norgen's Total RNA Purification 96-Well Kit allows for consistent isolation of both large and small RNA. Total RNA was isolated from samples of 5 x 105 HeLa cells using Norgen's Total RNA Purification 96-Well Kit. Aliquots of each total RNA sample were then used in 2 different RT-qPCR reactions. Ten microliters of the 75 µL isolated RNA were subjected to a 20 µL reverse transcription using miR-21 stem-loop reverse primer or oligo dT. Three microliters of the reverse transcription were used in a 20 µL real-time PCR reaction with primers to detect the human miR-21 (Panel A) and the S15 transcripts (Panel B), respectively. Both the mRNA and microRNA were amplified in a consistent manner from all the samples, with low variability of the Ct values. Thus both types of RNA are being consistently isolated using this kit.
Figure 13. Great Isolation Sensitivity. Norgen's Total RNA Purification Kit allows for sensitive RNA extraction from even less than 10 cells. RT-qPCR was used to detect mRNA isolated from various input amounts of HeLa cells, from 100,000 down to a single cell, using Norgen's Total RNA Purification 96-Well Kit. Ten microliters of the 75 µL isolated RNA were then subjected to a 20 µL reverse transcription using oligo dT primers. Three microliters of the reverse transcription were used in a 20 µL real-time PCR reaction with primers to detect the human S15 transcripts. The resulting Ct values were plotted against the input cell number. Total RNA was isolated and detected linearly from as little as a single HeLa cell.
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Kit Specifications
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Maximum Binding Capacity
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Up to 50 μg RNA
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Maximum Loading Volume
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650 μL
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Size of RNA Purified
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All sizes, including small RNA (< 200 nt)
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Maximum Amount of Starting Material
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| Animal Cells | 3 x 106 cells |
| Animal Tissues | 10 mg (for most tissues*) |
| Blood | 100 μL |
| Plasma/Serum | 200 μL |
| Bacteria | 1 x 109 cells |
| Yeast |
1 x 108 cells
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| Fungi |
50 mg
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| Plant Tissues |
50 mg
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| Time to Complete 10 Purifications |
20 minutes
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| Average Yield | |
| HeLa Cells (1 x 106 cells) | 15 μg |
| E. coli (1 x 109 cells) | 50 μg |
* for isolating total RNA from larger amounts of tissue, please use Norgen's Animal Tissue RNA Purification Kit (Cat# 25700)
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature. These kits are stable for 2 years after the date of shipment.
| Component | Cat. 17200 (50 preps) | Cat. 37500 (100 preps) | Cat. 17250 (250 preps) | Cat. 17270 (500 preps) | Cat. 24300 (192 preps) | Cat. 24370 (576 preps) | Cat. 24350 (192 preps) | Cat. 24380 (576 preps) |
|---|---|---|---|---|---|---|---|---|
| Buffer RL | 40 mL | 2 x 40 mL | 175 mL | 350 mL | 2 x 40 mL | 350 mL | 2 x 40 mL | 350 mL |
| Wash Solution A | 38 mL | 2 x 38 mL | 148 mL | 1 x 148 mL 1 x 74 mL |
2 x 38 mL | 1 x 74 mL 1 x 148 mL |
2 x 38 mL | 1 x 74 mL 1 x 148 mL |
| Elution Solution A | 6 mL | 2 x 6 mL | 30 mL | 60 mL | 2 x 20 mL | 60 mL | 2 x 20 mL | 60 mL |
| Mini Spin Columns | 50 | 100 | 250 | 500 | - | - | - | - |
| 96-Well Isolation Plate | - | - | - | - | 2 | 6 | - | - |
| 96-Well Isolation Plate (Deep Well) | - | - | - | - | - | - | 2 | 6 |
| Adhesive Tape | - | - | - | - | 4 | 12 | 4 | 12 |
| Collection Tubes | 50 | 100 | 250 | 500 | - | - | ||
| 96-Well Collection Plate | - | - | - | - | 2 | 6 | - | - |
| 96-Well Collection Plate (Deep Well) | - | - | - | - | - | - | 2 | 6 |
| Elution Tubes (1.7 mL) | 50 | 100 | 250 | 500 | - | - | ||
| 96-Well Elution Plate | - | - | - | - | 2 | 6 | - | - |
| 96-Well Elution Plate (Deep Well) | - | - | - | - | - | - | 2 | 6 |
| Product Insert | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
Poor RNA recovery could be due to one or more of the following:
Column/well clogging can result from one or combination of the following factors:
RNA can be degraded due to the following factors:
If the RNA does not perform well in downstream applications, it may be due to one or more of the following:
The contamination with genomic DNA may be due to large amount of starting material used. Perform RNase-free DNase I digestion on the RNA sample after elution to remove genomic DNA contamination. It is recommended that Norgen’s RNase-Free DNase I Kit (Product # 25710) be used for this step.
Yes, the Total RNA purification kits can be used to purify RNA from samples like buffy coats and isolated PBMCs. For blood leukocyte samples, you can use a specialized product - Leukocyte RNA purification kit.
Yes, Total RNA purification kits can be used with samples stored in RNA protective agents like RNAlater. Norgen Biotek also provides a similar RNA preserve solution (Cat. 17260).
Yes, you can use Total RNA purification kits to purify RNA from insect samples. Please contact our Tech support team at support@norgenbiotek.com and ask for reference publications.
Yes, lysates prepared in buffer RL can be frozen at -80°C, and the remaining protocol can be performed at a later date.
Yes, you can use Norgen's Total RNA purification kits with the aqueous phase from samples prepared in TRIzol. Please contact our Tech Support team at support@norgenbiotek.com if you have any questions regarding the protocol.
Yes, Norgen Total RNA purification kits are compatible with tissue samples stored in OCT compound. Please contact our Tech Support team at support@norgenbiotek.com and ask for reference publications.
| Title | Deep sequencing of the total RNA expression in CD24- and CD24+ mammary carcinoma Mvt1 cell line. |
| Citation | Genomics Data 2015. |
| Authors | R Rostoker, AD Jayaprakash, S Abelson, R Sachidanandam, D LeRoith |
| Title | Galnt1 Is Required for Normal Heart Valve Development and Cardiac Function |
| Citation | PLoS One 2015. |
| Authors | E Tian, SR Stevens, Y Guan, DA Springer, SA Anderson, MF Starost, V Patel, KG Ten Hagen, L Tabak |
| Title | LIN28A modulates splicing and gene expression programs in breast cancer cells |
| Citation | Molecular and Cellular Biology 2015. |
| Authors | J Yang, BD Bennett, S Luo, K Inoue, SA Grimm, GP Schroth, PR Bushel, HK Kinyamu, TK Archer |
| Title | Laser Capture Microdissection for Gene Expression Analysis |
| Citation | Methods in Molecular Biology 2015. |
| Authors | M Bidarimath, AK Edwards, C Tayade |
| Title | Metabolic and molecular responses in Nile tilapia, Oreochromis niloticus during short and prolonged hypoxia |
| Citation | Marine and Freshwater Behaviour and Physiology 2015. |
| Authors | Magdy E. Mahfouza*, Mona M. Hegazib, Mohammed A. El-Magdc& Enas A. Kasema |
| Title | Genes involced in sex pheromone biosynthesis of Ephestia cautella, an important food storage pest, are determined by transcriptome sequencing |
| Citation | BMC Genomics 2015. |
| Authors | B Antony, A Soffan, J Jakse, S Alfaifl, KD Sutanto, SA Aldosari, AS Aldawood, A Pain |
| Title | Early handling and repeated cross-fostering have opposite effect on mouse emotionality. |
| Citation | Frontieres in Behavioural Neuroscience 2015. |
| Authors | A Luchetti, D Oddi, V Lampis, E Centofante, A Felsani, M Battaglia, FR D'Amato |
| Title | Impact of s-Tocotrienol on Inflammatory Biomarkers and Oxidative Stress in Hypercholestrolemic Subjects |
| Citation | Clinical & Experimental Cardiology 2015. |
| Authors | AA Qureshi, DA Khan, W Mahjabeen, AM Trias, N Silswal, N Qureshi |
| Title | Associations between gastrointestinal toxicity, microRNA and cytokine production in pateients undergoing myeloablative allogeneic stem cell transplantation |
| Citation | International Immunopharmacology 2014. |
| Authors | PL Pontoppidan, K Jordan, AL Carlsen, HH Uhving, K Kielsen, M Christensen, M Ifversen, CH Nielsen, P Sangild, NH Heegaard, C Heilmann, H Sengelov, K Muller |
| Title | Identificationand sequence analysis of five allexiviruses species infecting garlic crops in Brazil |
| Citation | Tropical Plant Pathology 2014. |
| Authors | ML Oliveira, BR De Marchi, T Mituti, MA Pavan, R Krause-Sakate |
