C169 02

G6PD Deficiency Test

Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder which can cause haemolytic anaemia when people with the disorder come into contact with drugs, food and other substances which cause oxidative stress. G6PD deficiency is the most common enzyme deficiency worldwide. Diagnosis of G6PD deficiency is important in the treatment of disease because many oxidant drugs such as anti-malaria drugs, sulphur drugs and ascorbic acid cause a haemolytic anaemia especially for the G6PD deficient patients. Therefore, it is highly recommended to test for G6PD deficiency in patients before the treatment of oxidant drugs, especially for malaria patients, to protect against severe haemolytic anaemia. The CareStart G6PD deficiency test contains a strips in test device. The kit comprises of a single layer strip contained G6PD assay mixture. The assay is based on formazan method using tetrazolium compound. A whole blood sample with normal G6PD activity produces a purple colour in the reading window as it migrates to the strip. A whole blood sample deficient in G6PD activity shows no colour in the reading window.
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C184

New assays for specialist protein analyser

Six new assays have been added to the menu on Binding Site’s SPAplus Specialist Protein Analyser. These include IgG in cerebrospinal fluid (CSF), IgA CSF, IgM CSF, Albumin CSF as well as Transferrin in serum, and C1 inactivator (C1 inhibitor) in serum and plasma. All six assays are fully automated, easy to use and provide quantitative results to aid the assessment of a patient’s immune system (CSF assays), iron deficiency anaemia (transferrin) and the investigation of hereditary angioedema (C1 inactivator).The SPAplus is ideal for carrying out these specialist protein assays and has been designed to bring together instrument, reagents and exceptional support as a package from a specialist protein focused supplier.The analyser is a compact, turbidimetric platform for specialist protein testing. Its fully automated system enables laboratories to maintain the quality of results and high throughput required for specialised protein assays. It can be placed alongside the laboratory’s main-line analysers or in other areas of the laboratory. Pre-programmed protocols developed and manufactured by the company provide highly sensitive and reproducible results that match or have greater sensitivity than nephelometry. The modular design with intuitive Windows based software makes the analyser very easy to use. It is engineered to a high standard demonstrating excellent reliability with minimal daily, weekly and monthly maintenance procedures.
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C182

Automated cervical cancer sample preparation

A walk-away automated system for cervical cancer slide preparation, ThinPrep 5000 is capable of processing up to 20 gynaecological (or general cytology) slides per batch utilising ThinPrep technology for dispersion, collection and transfer of cells. During dispersion the sample vial is spun to separate debris and mucus and to randomise the cells. These are then collected on the exterior surface of the Pap test filter with the help of a vacuum and software that monitors the rate of flow. Finally the cells are transferred to a defined circular area on a microscope slide for examination. Thirty-five slides can be processed per hour.
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C183

Fully automated MRSA assay

The challenge to fight healthcare-associated infections in Europe is resulting in an increased number of active surveillance programmes for MRSA in a continually resource-constrained environment. Rapidly and accurately identifing methicillin-resistant Staphylococcus aureus (MRSA) in patients, the BD MAX MRSA assay enables infection control measures to be implemented faster, which can positively impact patient management. The fully automated, bench-top molecular system is designed to perform a broad range of molecular testing as well as the MRSA assay. This offers laboratory professionals the flexibility and versatility to perform CE/in vitro diagnostic assays and user defined protocols on the same platform.
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C187

Diagnostics for the early detection and management of hepatitis C infection

Early detection of HCV infection is vital in order to provide consolidated care of acute and chronic infection, and adequate treatment of drug response monitoring is crucial to overall therapy success. Patients undergoing a peginterferon alfa-2a and ribavirin therapy can be monitored precisely by real-time PCR measurement. The novel Elecsys anti-HCV II immunoassay on cobas e modules allows the early qualitative detection of antibodies against HCV. The updated assay delivers enhanced convenience, specificity, increased reliability and consistency for improved efficiency in screening patients as well as blood donors. Following the identification of HCV antibodies, testing for HCV RNA, which is a crucial marker in the management of hepatitis C, confirms the infection and facilitates prediction of treatment response. Sensitive HCV RNA qualitative and quantitative tests to measure viral load and predict drug response are available on the COBAS AmpliPrep/COBAS TaqMan fully automated platform.
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ELISA for sarcopenia

Sarcopenia is defined as the loss of skeletal muscle mass and strength that can occur with advancing age. The current diagnosis of the disease is by dual-emission X-ray absorptiometry (DXA) scan, which measures lean body mass (LBM) in combination with functional tests. This cumbersome technique provides no information on the underlying cause of the loss of LBM. A novel biomarker is now available to identify the subgroup of patients (40%), whose sarcopenia is caused by excessive neurotrypsin activity. The NTCAF ELISA test has initially been developed for research purposes to aid the development of a treatment for the condition and could have potential as a companion diagnostic.
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C01 pn

Automated rotary microtome

A fully automated rotary microtome with four mechanised cutting modes, the Thermo Scientific HM355S delivers exceptional quality sections across an extensive range of specimen types. Concern for operator safety is integral to the design with an obvious Emergency Stop, manual and electronic braking mechanisms and a unique double-tap start function ensuring only intentional operation, protecting both the user and the specimen from accidental damage. The long 72mm vertical cutting stroke, large wraparound waste tray, programmable cutting window and memory positioning all contribute in streamlining workflow and improving sectioning efficiency, for specimens up to SuperMega cassette size.
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C189

Mass spectrometer for routine quantitation

A new triple quadrupole system is available that delivers 10x better sensitivity than triple quadrupole systems in the same mid-level class. The TripleQuad 4500 system with industry-leading ruggedness is designed to be the new ‘workhorse’ mass spectrometer. With the option of QTRAP technology, which increases full-scan sensitivity by 100x over basic triple quadrupoles by incorporating the Linear Accelerator Trap, unmatched levels of confidence in results are provided. To simplify the adoption of this next generation of LC/MS/MS technology, bundled solution packages (Accelerated Lab Integration Packages) are offered consisting of the mass spectrometer, but also the standards, software, training, validation services and a liquid chromatography (LC) system, including the new Eksigent ekspert ultra 100 and 100-XL systems. These are analytical flow rate LC systems. With the new 4500 series, laboratory analysts are able to significantly improve results for a variety of applications, including clinical research, forensic toxicology, protein identification, peptide quantitation and bioanalysis.
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C190

Cryptosporidium/Giardia enzyme immunoassay

Cryptosporidiosis is routinely diagnosed by microscopic analysis of stool samples using organic dyes, or by immunostaining with direct fluorescent antibody, and it can be difficult to detect. Similarly, Giardia lamblia infection is frequently misdiagnosed, relying on poorly performing antigen-based testing. A new enzyme immunoassay (EIA) for the qualitative detection of Cryptosporidium and G. lamblia antigens in human faecal specimens from patients displaying gastrointestinal symptoms, the Prolisa Cryptosporidium/Giardia EIA kit offers precise results with high sensitivity and excellent specificity, enabling accurate diagnosis of infection. This convenient, rapid and easy-to-use method of detecting Cryptosporidium and G. lamblia is supplied in a 96-well test size consisting of detachable stripwells. This assay uses monoclonal anti-Cryptosporidium and anti-G. lamblia antibodies to ensure excellent sensitivity and specificity for high value diagnostic results. It can be performed manually as well as on most automated platforms for increased workflow flexibility.
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C208

Rheumatoid Factor (RF)/IgG absorbent reagent

Specifically designed for IVD manufacturers for use in conjunction with immunodiagnostic assays, Binding Site’s RF/IgG absorbent reagent is distinctively formulated to remove both IgG and RF-IgM molecules from human serum. In principle, the reagent effectively prevents these components from non-specific binding within the test sample. This eliminates certain interference effects found with some immunodiagnostic assays that are aimed at quantitatively determining human antigen-specific IgM immunoglobulin concentrations, as found in various diagnostic disease states. As such, the RF/IgG Absorbent Reagent serves to enhance overall specificity by reducing both the number of false positive test results from native IgG components and the number of false negative test results from native RF-IgM components. The reagent demonstrates outstanding performance characteristics in routine use, and is available as a ready-to-use, fully liquid stable product offered in a number of convenient, operator-oriented packaging configurations, including bulk-sized formats.
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