
Norgen Stool DNA Isolation Kit Dx
CE-IVDR 인증을 받은 진단용 대변 DNA 정제 키트로, 숙주 및 미생물 DNA를 동시에 빠르고 간편하게 추출합니다. PCR 저해물 제거로 고품질 DNA 확보, Norgen 보존 튜브와 완벽 호환, 다양한 분자진단 및 NGS 응용에 적합합니다.
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Norgen Stool DNA Isolation Kit Dx
SKU: Dx27600
For the rapid and simple purification of bacterial and host DNA from stool and fecal samples for in vitro diagnostic use.
Features and Benefits
- CE-IVDR marked in accordance with European Commission Regulation (EU) No. 2017/746
- Ideal for use in in vitro diagnostic workflows
- Simultaneous isolation of both host DNA and microbial DNA (universal protocol)
- Eliminates PCR inhibitors including humic acids
- Fully compatible with Norgen’s Stool Nucleic Acid Collection and Transport Tubes
- High-quality DNA for sensitive downstream applications including PCR, qPCR, sequencing, and microarray
This kit provides a convenient and rapid method to isolate total DNA from fresh, frozen, and preserved stool samples, including those preserved using Norgen’s Stool Nucleic Acid Collection and Preservation Devices Dx (Cat. Dx45660).
The universal protocol allows simultaneous isolation of total genomic DNA from microorganisms and host cells.
All traces of humic acids and other inhibitors are removed using Bead Tubes and a combination of chemical and physical homogenization and lysis, without phenol-chloroform extraction.
A simple spin column procedure yields high molecular weight DNA (up to 50 kb+), suitable for PCR, qPCR, NGS, and microarray applications.
NOTE: This product is not available for sale in the United States.
Kit Specifications
| Specification | Description |
|---|---|
| Maximum Stool Input | 200 mg (fresh/frozen) or 400 μL (preserved) |
| Type of Stool Processed | Frozen, fresh, or preserved stool |
| Format | Spin Column |
| Maximum Column Binding Capacity | 50 μg |
| Maximum Column Loading Volume | 650 μL |
| Elution Volume | 50 μL |
| Time to Complete 10 Purifications | 30 minutes |
| Applications | PCR, qPCR, Southern Blot, Sequencing, Microarray Analysis |
Storage Conditions and Product Stability
All solutions should be kept tightly sealed and stored at room temperature.
This kit is stable for 2 years after the date of shipment.
| Component | Cat. Dx27600 (50 preps) |
|---|---|
| Lysis Solution | 60 mL |
| Lysis Additive | 6 mL |
| Binding Solution | 7 mL |
| Wash Solution I | 30 mL |
| Wash Solution II | 22 mL |
| Elution Buffer | 3 mL × 2 |
| Bead Tube | 50 |
| Mini Spin Columns | 50 |
| Collection Tubes | 50 |
| Elution Tubes (1.7 mL) | 50 |
| Product Insert | 1 |
Supporting Data
Figure 1. Higher Yields of DNA than Competitor Z
Stool DNA was isolated from 200 mg of fresh stool samples using Norgen’s Stool DNA Isolation Kit Dx and Competitor Z’s Kit.
10 µL of DNA from the elution was run on 1X TAE 1.2% agarose gel.
Norgen’s kit isolated much higher yields of DNA.
Marker = Norgen’s HighRanger DNA Ladder.
| Norgen | Competitor Z |
|---|
Figure 2. Higher Quality DNA than Competitor Z
DNA quality measured by Nanodrop. Norgen’s Stool DNA Isolation Kit Dx isolated DNA of the highest quality.
| Sample | A260/280 (OD) | A260/230 (OD) |
|---|---|---|
| Norgen | ~2.0 | ~1.5 |
| Competitor Z | ~1.0 | ~0.3 |
Figure 3. High Quality DNA confirmed by Real-time PCR
Stool DNA was isolated from 200 mg of fresh stool samples using Norgen’s kit and Competitor Z’s kit.
DNA quality confirmed by real-time PCR detecting 16S rRNA.
Earlier Ct values with Norgen’s samples indicate higher quality DNA.
Amplification Graph Parameters
- Y-axis: RFU (Relative Fluorescence Units) [0–2000]
- X-axis: Cycles [0–40]
Figure 4. Taxonomic Classifications of 10 Fecal Microbiomes
A) Principal Coordinate Analysis (PCoA) showing taxonomic distribution up to class level.
B) Hierarchical clustering based on genus-level classifications.
| Axis | Label |
|---|---|
| X-axis | Principal Coordinate 2 |
| Y-axis | Principal Coordinate 1 |
Taxonomic Levels: Kingdom, Phylum, Class, Order, Family, Genus, Species
Documentation
Protocols
Application Notes
- Detection of Viral, Bacterial and Human Genomic DNA From Preserved Stool Samples
- Quantitative Adenovirus Detection Using Taqman Real-time PCR
- Comparative Study of DNA Isolated from Stool Using Norgen’s Kits
- Comparison of Stool DNA Isolation Methods
- Determination of DNA Molecular Weight
- Gut Microbiome Diversity: Comparison of Preservation Methods
Safety Data Sheets
Flyers
Citations
| Title | Journal | Authors |
|---|---|---|
| Changes on fecal microbiota in rats exposed to permethrin during postnatal development | Environmental Science and Pollution Research International (2016) | Nasuti C et al. |
| Independent Evaluation of CryoXtract Instruments’ CXT350 | Biopreservation and Biobanking (2016) | Mathieson W et al. |
| Cryptosporidiosis outbreak in a child day-care center | Enfermedades Infecciosas y Microbiología Clínica (2015) | Pilar Goñi et al. |
| Detection of Campylobacter in human faecal samples in Fiji | Western Pacific Surveillance and Response Journal (2014) | Aruna Devi et al. |
| DNA-based diagnostic tools in veterinary parasitology | Veterinary Parasitology (2011) | Hunt PW, Lello J |
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