RNA/DNA Purification Kits
For research use only and NOT intended for in vitro diagnostics.
RNA/DNA Purification Kits
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Supporting Data
Figure 1. Recovery of True Total RNA including microRNA from Hamster Heart. Panel A is a 1X MOPS 1% agarose gel showing the RNA that was isolated from 2 different samples of 10 mg hamster heart using Norgen's RNA/DNA Purification Kit. Norgen's RNA/DNA Purification Kit isolated large RNA (represented by 28S and 18S rRNA) with high integrity. Moreover, it provided the added benefit of recovering small RNA without any additional protocol. Panel B is a result from a bioanalyzer resolution of the eluted RNA. Similar to the agarose gel, Norgen's RNA/DNA Purification Kit showed the added benefit of recovering small RNA. The effectiveness of small RNA recovery was also demonstrated by gene-specific RT-qPCR. One microgram of RNA was used in RT-qPCR reactions for human S15 (for Large RNA) and miR-21 (for microRNA) genes. The RNA isolated by Norgen’s RNA/DNA Purification Kit showed detection of both small RNA (Panel C) and the large RNA (Panel D).
Figure 2. Recovery of Intact, High Quality Genomic DNA from Hamster Heart. Panel A is a 1% agarose gel showing the gDNA isolated from the same hamster heart samples above using Norgen's RNA/DNA Purification Kit. Lane M is Norgen's HighRanger 1 kb DNA Ladder and the sample lanes contain 10 µL of each of the 100 µL elutions. The gel showed high quality, and intact genomic DNA. Panel B is the result of qPCR amplification of 25 ng of eluted genomic DNA using 5S rRNA-specific primers. Genomic DNA isolated using Norgen's RNA/DNA Purification Kit is of high quality with effective qPCR amplification.
Figure 3. Recovery of True Total RNA including microRNA from Hamster Liver. Panel A is a 1X MOPS 1% agarose gel showing 3 µL of 20 µL eluted RNA that was isolated from 2 different samples of 5 mg hamster liver using Norgen's RNA/DNA Purification Micro Kit. Norgen’s RNA/DNA Purification Micro Kit isolated large RNA (represented by 28S and 18S rRNA) with high integrity. Moreover, it provided the added benefit of recovering small RNA without any additional protocol. Panel B is a result from a bioanalyzer resolution of the eluted RNA. Similar to the agarose gel, Norgen's RNA/DNA Purification Micro Kit showed the added benefit of recovering small RNA while isolating very high quality RNA. The effectiveness in small RNA recovery was also demonstrated by gene-specific RT-qPCR. One microgram of RNA was used in RT-qPCR reactions for beta-Actin (for Large RNA) and miR-21 (for microRNA) genes. The RNA isolated by Norgen’s RNA/DNA Purification Micro Kit showed detection of both small RNA (Panel C) and the large RNA (Panel D).
Figure 4. Recovery of Intact, High Quality Genomic DNA from Hamster Liver. Panel A is a 1% agarose gel showing the gDNA isolated from the same hamster liver samples using Norgen’s RNA/DNA Purification Micro Kit. Lane M is Norgen's HighRanger 1 kb DNA Ladder and the sample lanes contain 3 µL of each of the 20 µL elutions. The gel showed high quality, and intact genomic DNA. Panel B is the result of qPCR amplification of 25 ng of eluted genomic DNA using 5S rRNA-specific primers. Genomic DNA isolated using Norgen’s RNA/DNA Purification Micro Kit is of high quality with effective qPCR amplification.
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Kit Specifications
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Maximum Column Binding Capacity
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50 μg for RNA
20 μg for DNA |
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Maximum Column 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) |
| Maximum Amount of Starting Material: Animal Cells Animal Tissues Blood Bacteria Yeast Fungi Plant Tissues |
5 x 106 cells 25 mg (for most tissues)** 200 μL 1 x 109 cells 1 x 108 cells 50 mg 50 mg |
| Time to Complete 10 Purifications |
30 minutes
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Average Yield*:
HEK 293 Cells (1 x 106 cells) HEK 293 Cells (1 x 106 cells) Liver (15 mg) Liver (15 mg) |
10-15 μg RNA 2-4 μg DNA 30-35 μg RNA 4-6 μg DNA |
*Average Yield will vary depending upon a number of factors including species, growth conditions used, and development stage.
**Tissue inputs of up to 40 mg may be used, however for inputs greater than the recommended 25 mg, cross-contamination of the RNA and DNA fractions is possible.
Storage Conditions and Product Stability
Store Proteinase K at -20°C upon arrival. All other solutions should be kept tightly sealed and stored at room temperature. This kit is stable for 1 year after the date of shipment.
| Component | Cat. 48700 (50 preps) | Cat. 50300 (50 preps) |
|---|---|---|
| Buffer SKP | 40 mL | 40 mL |
| Wash Solution A | 2 x 38 mL 1 x 18 mL |
2 x 38 mL 1 x 18 mL |
| Elution Solution A | 6 mL | 6 mL |
| Elution Buffer F | 15 mL | 6 mL |
| RNase-Free Water | 40 mL | 40 mL |
| Proteinase K | 2 x 12 mg | 2 x 12 mg |
| gDNA Purification Columns | 50 | - |
| gDNA Purification Micro Columns | - | 50 |
| RNA Purification Columns | 50 | - |
| RNA Purification Micro Columns | - | 50 |
| Collection Tubes | 100 | 100 |
| Elution Tubes (1.7 mL) | 100 | 100 |
| Product Insert | 1 | 1 |
Documentation
FAQs
Spin Column, Micro
Poor DNA recovery may be caused by one or more of the following:
- Incomplete lysis of cells or tissue. Ensure that the appropriate amount of Buffer SKP was used for the amount of cells or tissue.
- Column has become clogged. Do not exceed the recommended amounts of starting materials. The amount of starting material may need to be decreased if the column shows clogging below the recommended levels. See FAQ related to “Clogged Column” below.
- An alternative elution solution was used. It is recommended that the RNA Elution Buffer supplied with this kit be used for maximum RNA recovery.
- Ethanol was not added to the lysate. Ensure that the appropriate amount of ethanol is added to the lysate before binding to the column.
- Ethanol was not added to the Wash Solution A. Ensure that 96 – 100 % ethanol is added to the supplied Wash Solution prior to use.
- Low RNA content in cells or tissues used. Different tissues and cells have different RNA contents, and thus the expected yield of RNA will vary greatly from these different sources. Please check literature to determine the expected RNA content of your starting material.
- Cell Culture: Cell monolayer was not washed with PBS. Ensure that the cell monolayer is washed with the appropriate amount of PBS in order to remove residual media from cells.
- Yeast: Lyticase was not added to the Resuspension Buffer. Ensure that the appropriate amount of lyticase is added when making the Resuspension Buffer.
- Bacteria and Yeast: All traces of media not removed. Ensure that all media is removed prior to the addition of the Buffer SKP through aspiration.
Column clogging may occur due to:
- Maximum number of cells or amount of tissue exceeds kit specifications. Refer to specifications to determine if the amount of starting material falls within kit specifications.
- Centrifuge temperature is too low. Ensure that the centrifuge remains at room temperature throughout the procedure. Temperatures below 20°C may cause precipitates to form that can cause the columns to clog.
Eluted RNA can be degraded due to the following factors:
- RNase contamination. RNases may be introduced during the use of the kit. Ensure proper procedures are followed when working with RNA. Please refer to “Working with RNA” at the beginning of this user guide.
- Procedure not performed quickly enough. To maintain the integrity of the RNA, it is important that the procedure be performed quickly. This is especially important for the Cell Lysate Preparation Step in the Animal Tissue protocol, as RNA in animal tissues is not protected after harvesting until it is disrupted and homogenized. Also, after the DNA binding step, the flowthrough should be kept on ice or –20°C if the RNA purification step is not carried out immediately.
- Improper storage of the purified RNA. For short-term storage, RNA samples may be stored at –20°C for a few days. It is recommended that samples be stored at –70°C for longer-term storage.
- Frozen tissues or cell pellets were allowed to thaw prior to RNA isolation. Do not allow frozen tissues to thaw prior to grinding with the mortar and pestle to ensure that the integrity of the RNA is not compromised.
- Lysozyme or lyticase used may not be RNase-free. Ensure that the lysozyme and lyticase being used with this kit are RNase-free to prevent possible problems with RNA degradation.
- Tissue samples were frozen improperly. Samples should be flash-frozen in liquid nitrogen and transferred immediately to a –70°C freezer for long-term storage.
If the RNA does not perform well in downstream applications, it may be due to one or more of the following:
- RNA was not washed twice with the provided Wash Solution A. Traces of salt from the binding step may remain in the sample if the column is not washed twice with Wash Solution A. Salt may interfere with downstream applications, and thus must be washed from the column.
- Ethanol carryover. Ensure that the dry spin under the RNA Wash procedure is performed to remove traces of ethanol prior to elution. Ethanol is known to interfere with many downstream applications.
