We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Stool DNA Extraction Kit for Molecular Diagnostics Faster, Simpler

By LabMedica International staff writers
Posted on 16 Aug 2011
A DNA extraction kit provides a faster, simpler method to purify genomic DNA from stool samples prior to PCR amplification and analysis.

The E-Sphere stool DNA extraction kit answers the market need for speed with the added benefits of accuracy, improved cost effectiveness, reduced risk of sample contamination, and greater safety for lab technicians. The process requires only standard clinical laboratory equipment.

Image: The E-Sphere stool DNA extraction kit (Photo courtesy of Phthisis Diagnostics).
Image: The E-Sphere stool DNA extraction kit (Photo courtesy of Phthisis Diagnostics).

Advanced technology in the kit includes the high performance E-Sphere stool enzyme, a thermostable reagent that digests fecal matter at 75 °C during the 15-minute incubation stage. A further innovation is the proprietary E-Sphere clean-up column, which purifies the DNA.

Phthisis Diagnostics (Charlottesville, VA, USA) introduced the kit at the American Society for Microbiology annual meeting, which took place during May 21-24, 2011, in New Orleans (LA, USA). The kit allows lab workers to extract DNA from human stool samples in a three-step process. Other similar kits take three times the steps, said company cofounder and president Crystal Icenhour.

The E-Sphere stool sample-preparation method allows manual DNA extraction from 12 stool samples in less than 30 minutes. The process includes only nine steps and minimizes sample contamination risk with just 2 sample transfers. Stool samples can be quickly processed within a biological safety cabinet.

The kit was developed and manufactured in the USA to International Organization for Standardization (ISO) 9001 & ISO 13485 standards in a Quality Systems Registrars (QSR) & current Good Manufacturing Practice (cGMP) compliant facility, and is designated as a general-purpose reagent.

Related Links:

Phthisis Diagnostics


New
Gold Member
Flocked Fiber Swabs
Puritan® Patented HydraFlock®
Unit-Dose Packaging solution
HLX
New
Thyroid Stimulating Hormone Assay
Neonatal TSH ELISA Kit
New
Clinical Sample Concentrator
QIAamp DSP Virus Kit

Latest Molecular Diagnostics News

Simple Blood Draw Helps Diagnose Lung Cancer 10 Times Faster

WHO Approves First Mpox Diagnostic Test for Emergency Use

Clinical Digital PCR System for Oncology Testing Delivers Highly Accurate Diagnostic Results