Customize Consent Preferences

We use cookies to help you navigate efficiently and perform certain functions. You will find detailed information about all cookies under each consent category below.

The cookies that are categorized as "Necessary" are stored on your browser as they are essential for enabling the basic functionalities of the site. ... 

Always Active

Necessary cookies are required to enable the basic features of this site, such as providing secure log-in or adjusting your consent preferences. These cookies do not store any personally identifiable data.

No cookies to display.

Functional cookies help perform certain functionalities like sharing the content of the website on social media platforms, collecting feedback, and other third-party features.

No cookies to display.

Analytical cookies are used to understand how visitors interact with the website. These cookies help provide information on metrics such as the number of visitors, bounce rate, traffic source, etc.

No cookies to display.

Performance cookies are used to understand and analyze the key performance indexes of the website which helps in delivering a better user experience for the visitors.

No cookies to display.

Advertisement cookies are used to provide visitors with customized advertisements based on the pages you visited previously and to analyze the effectiveness of the ad campaigns.

No cookies to display.

D6364 MagPure Stool DNA Kit

Facebook
X
Pinterest
Email

MagPure Stool DNA Kit is specially designed for high throughput DNA extraction from stool samples. It can get high purity microbial DNA from stool samples (≤200mg). This kit is based on magnetic beads purification and unique inhibiting factors adsorption technology, no phenol-chloroform extraction or alcohol precipitation. It can adsorb humic acid and other inhibiting factors in the solution efficiently. DNA can be directly used for downstream applications such as PCR, Viral DNA testing, bacterial DNA testing, etc.

Detail

Introduction

MagPure Stool DNA Kit is specially designed for high throughput DNA extraction from stool samples. It can get high purity microbial DNA from stool samples (≤200mg). This kit is based on magnetic beads purification and unique inhibiting factors adsorption technology, no phenol-chloroform extraction or alcohol precipitation. It can adsorb humic acid and other inhibiting factors in the solution efficiently. DNA can be directly used for downstream applications such as PCR, Viral DNA testing, bacterial DNA testing, etc.

Details

Specifications

FeaturesSpecifications
Main FunctionsIsolation total DNA from 100-150mg stool samples
ApplicationsPCR, southern blot and enzyme digestion, etc.
Purification technologyMagnetic beads technology
Process methodManual or automatic
Sample typeStool
Sample amount100-150 mg
Elution volume
Time per run

Principle

This product is based on the purification method of high binding magnetic particles. The sample is lysed and digested under the action of lysate and Lysozyme. DNA is released into the lysate. After adding magnetic particles and binding solution, DNA will be adsorbed on the surface of magnetic particles, and impurities such as proteins will be removed without adsorption. The adsorbed particles were washed with washing solution to remove proteins and impurities, washed with ethanol to remove salts, and finally DNA was eluted by Elution Buffer.

Advantages

  • Fast – several samples can be extracted in 60 minutes (after digestion)
  • High purity – unique adsorbent can completely remove inhibitory factors
  • High recovery – DNA can be recovered at the level of PG

Kit Contents

ContentsD6364
Purification Times400 Preps
MagPure Particles N14 ml
2ml Bead Tubes400
PVP-106 g
RNase A75 mg
Proteinase K180 mg
Protease Dissolve Buffer20 ml
Buffer ATL300 ml
Buffer PCI300 ml
Buffer MLE180 ml
Buffer GW1*132 ml
Elution Buffer60 ml

Storage and Stability

MagPure Particles, RNase A and Proteinase K should be stored at 2-8°C upon arrival. However, short-term storage (up to 24 weeks) at room temperature (15-25°C) does not affect their performance. The remaining kit components can be stored dry at room temperature (15-25°C) and are stable for at least 18 months under these conditions.

Other Products

6x1000ml Angle Rotor 

EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Kits

Overview

  • Ensure optimal results for sensitive applications like NGS
  • Up to a tenfold increase in microRNA mapping during sequencing runs to reduce costs
  • Purification and enrichment of intact cell culture media exosomes for functional studies
  • No phenol extractions, Proteinase K treatment, nor carrier RNA required
  • No time-consuming ultracentrifugation, filtration nor special syringes required
  • No precipitation reagents nor overnight incubation required
  • Pure exosomes are purified and are free-from any other RNA-binding proteins
  • Purification is based on EXTRAClean spin column chromatography that uses Norgen’s proprietary resin separation matrix

Norgen’s EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Kits constitute all-in-one systems for the purification of exosomes and the subsequent isolation of RNA from different cell culture media sample volumes. The purification is based on spin column chromatography that employs Norgen’s proprietary resin. The EXTRAClean columns undergo stringent processing and rigorous quality control measures to minimize contamination traces, ensuring optimal results for sensitive applications such as NGS. The kit is designed to isolate all sizes of RNA, including microRNA. The kit provides a clear advantage over other available kits in that it does not require any special instrumentation, protein precipitation reagents, extension tubes, phenol/chloroform or protease treatments. Moreover, the kits allows the user to elute into flexible elution volumes ranging from 50 μL to 100 μL. The purified RNA is free from any protein-bound circulating RNA and is of the highest integrity. The purified RNA can be used in a number of downstream applications including real time PCR, Sequencing based applications, reverse transcription PCR, Northern blotting, RNase protection and primer extension, and expression array assays.

Details

Supporting Data

Figure 1 / 9

Previous

Average read quality distribution relative to raw reads of small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Mini Kit. Calculations were relative to raw reads.
Average read quality distribution relative to raw reads of small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Mini Kit. Calculations were relative to raw reads.
Genome mapping distribution relative to input reads obtained from small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Mini Kit.
Average small RNA biotype distribution relative to the input reads obtained from sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Mini Kit.
Average read quality distribution relative to raw reads of small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Midi Kit. Calculations were relative to raw reads.
Genome mapping distribution relative to input reads obtained from small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Midi Kit.
Average small RNA biotype distribution relative to the input reads obtained from sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Midi Kit.
Average read quality distribution relative to raw reads of small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Maxi Kit. Calculations were relative to raw reads.
Genome mapping distribution relative to input reads obtained from small RNA sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Maxi Kit.
Average small RNA biotype distribution relative to the input reads obtained from sequencing of exosomal RNA extracted from various cell culture media volumes using EXTRAClean Cell Culture Media Exosome Purification and RNA Isolation Maxi Kit.

Next

Click for expanded view

Sample TypeCell-Free Cell Culture Media
Sample Volume Range5 ml to 10 mL
Size of RNA PurifiedAll sizes, including miRNA and small RNA (< 200 nt)
Elution Volume50-100 μL
Time to Complete 10 Purifications35-40 minutes
Average YieldsVariable depending on specimen

Storage Conditions and Product Stability
All buffers should be kept tightly sealed and stored at room temperature. This kit is stable for 2 years after the date of shipment. It is recommended to warm Lysis Buffer A for 20 minutes at 60°C if any salt precipitation is observed.

One Step Isothermal Basic RNA Amplification Kit For High Throughput RNA Analysis

One Step Isothermal Basic RNA Amplification Kit For High Throughput RNA Analysis

Product Description

     One-Step Isothermal Amplification Basic Kit for High Throughput RNA Analysis

  Product Detail

Kit Storage and Term of Validity

Storage term: stored at ≤-20℃,keep away from light, avoid heavy weight and repeated freezing and thawing.

Term of Validity: 14 months

Isothermal Nucleic Acid Principle Summary

This kit is based on a rapid nucleic acid amplification technology at room temperature and constant temperature:at room temperature and constant temperature(generally 39℃~42℃),reverse transcriptaseuses specific primers and template RNA tosynthesize cDNA strands,and binds the auxiliary protein and single strand with the help of the protein, the recombinase and the primer form a complex; perform a homology search and bind the target homology domain, at this time a D-loop region is formed at the homology positionand strand exchange begins; accompanied by the recombinase from the complex upon dissociation,the polymerase also bindsto the 3′ end of the primer,initiating chainextension.It is suitable for laboratory-level RNA amplification and RNA amplification for other detection purposes.

Technical Parameters:

ParametersDetails
Product NameRNA Isothermal Amplification Kit Basic
ManufacturerAmp-future
Storage Temperature-20°C
Kit ComponentsEnzymes, Buffers ,Reagents
Packaging48 Tests/box
Detection Limit500-1000copies/µL
ShippingICE
Test Time5-20mins

Isothermal Nucleic Acid Product Features

1/ High sensitivity and specificity, short reaction time.

2/ The reagent form is freeze-dried, stable and easy to operate.

3/ The reaction can be operated by metal bath and water bath pot without purchasing expensive PCR apparatus.

Isothermal Nucleic Acid Applications

Suitable for RNA isothermal rapid amplification kit(BASIC type)

Primer: Require pair of nucleotide primers with the length of 25-35 bp.

RNA basic kit reaction temperature is 39 to 42℃ and time is 5-20 minutes.

Notes

1/ Please avoid nucleic acid contamination and set blank control during reaction due to the high sensitivity of the kit.

2/ Please take out the required quantity of MIRA reaction units for the experiment, and put the rest under storage conditions when performing the experiment.