AES .....from sample collection... ...to final results!
An international leader in rapid microbiology technologies such as flow and laser scanning cytometry, molecular biology, culture media and metrology. Providing solutions for sample collection, sample preparation, ready-to-use culture media and automated media preparation, inoculation and incubation & temperature monitoring. PCR diagnostic kitsets are also available.
The coolrack company. Cool, thaw, freeze, snap-freeze - consistent temperature control for all lab and biomedical samples. Precision tools to provide accuracy and reproducibility whether this be Test to Test, User to User, Lab to Lab or Site to Site.
The CultureStat Rapid UTI Detection System represents a significant advance in the area of urine culture testing. The system is a self-contained total microbe test which objectively determines the presence or non-presence of log phase bacteria by light spectrophotometry and computer-driven statistical analysis. Compact, portable and extremely easy to use, the CultureStat Rapid UTI Detection System dramatically improves the practice of testing for urinary tract infections in hospitals and independent laboratories.
Innovative sample preparation and protein purification tools for research scientists and clinical customers in public sector institutes and industry. Products include BJP static ultrafiltration concentrators for the clinical customer, Proteus rapid protein purification kit products for life science research markets that support both antibody and his-tagged protein purification.
World leading supplier of automated colony counters and zone measurement systems for any microbiology application.
The hallmark of all Synbiosis systems is their outstanding automation, which is guaranteed to improve both the throughput and accuracy of results and in turn the productivity of the laboratory. The products can be used in a wide range of laboratories covering food and environmental monitoring through to clinical and pharmaceutical applications as all systems are designed to adhere to GLP and the software behind the systems can be easily integrated into a 21 CFR Part 11 environment. Extensive IQ/OQ/PQ validation information can also be provided to meet the most rigorous accreditation checks or regulatory requirements.
