The Selectra Touch Pro Software for the Selectra Pro S and Pro M Clinical Chemistry Systems provides touch screen operation with intuitive design and significantly boosts laboratory productivity, reduces errors and offers detailed traceability of results. The smart colour icons guide the operator through the daily operation with minimum effort. Auto validation with 40 laboratory configurable criteria speeds results as qualified test results are sent directly to the LIS and operators can focus on exceptions. Real time individual data are traceable and archived for each result including operator, QC, calibration, control, absorbance, and reagent lot expiration. Reagents, test parameters, calibration and control values are programmed automatically via barcode with inventory tracked in real time. Maintenance tasks are automated, tracked and set up to run when the analyser is not in use. Automated and customizable start and end of day checklists ensure all essential tasks are completed. Remote access diagnostics provide real time support, helping to decrease both downtime and costs. Interactive learning through a dedicated online training website includes maintenance modules to assist operators at all times. Read more
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Globe Scientific’s Uniplast™ plastic serological pipettes feature a onepiece construction designed to eliminate the risk of breakage and sample retention. Clear black graduation marks prevent ambiguity and guarantee precise liquid reading and >98% accuracy. The serological pipettes are produced from crystal clear virgin polystyrene (PS) and are colour coded for easy volume identification. The calibration of the pipettes is certified for accuracy. Each pipette has a bonded polyolefin aerosol barrier plug to prevent pipettor contamination. The specially designed tip provides the best fill and release rates. Sterile pipettes are RNase-free, DNase-free, non-pyrogenic, non-hemolytic and non-cytotoxic. Manufactured under strict ISO 9001:2008 quality standards. they are available in 1mL, 2mL, 5mL, 10mL and 25mL sizes. Read more
Expanding Bio- Systems’ fertility line portfolio, the Fertility Biochemistry Control is a lyophilized control (1 mL) containing component concentration suitable for the quality control of fertility testing in clinical laboratories: Citrate, Fructose and Zinc. This new product complements the company’s line for laboratories dedicated to fertility control. Read more
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Designed for the measurement of MxA protein in human whole blood, an innovative ELISA based on the use of patented monoclonal antibodies and a special buffer to extract the cytoplasmic MxA protein is suitable for the monitoring of IFN-β therapy in multiple sclerosis patients and for viral infection recognition. Human Myxovirus protein A is induced exclusively by IFN-α and IFN-β. Since direct measurement of the IFN levels in plasma is difficult, MxA may be useful as a marker distinguishing viral disease from bacterial infection or from acute graft-versus-host disease after allogenic stem cell transplantation. Neutralizing antibodies may develop during the IFN-β therapy of multiple sclerosis and lead to loss of drug bioactivity. The IFN-β-inducible MxA protein is an ideal marker of IFN-β bioavailability, capable of discriminating between biologically responsive and non-responsive patients. The BioVendor assay meets all the requirements for routine clinical use in manual mode as well as on open ELISA robotic systems. Read more
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Designed for daily use in small labs and providing all the qualities of a high throughput qualitative instrument at an affordable rate, the ZENIX 2200 features a high quality optical system, using semi-reflective mirrors and cuvettes with excellent UV penetrability for the same level of sensitivity as the best systems on the market. Efficiency is increased thanks to its independent washing station, 44 reagent and 44 sample capacity rotors and its comprehensive software compatible with Windows® 7, Vista and XP. With a throughput of 200 tests/hour, the instrument also uses automatic dilution and retesting when concentrations are outside limits. Its maintenance-free micro pump and easy access to internal systems optimize maintenance and allow for quick and easy servicing. Read more
https://clinlabint.com/wp-content/uploads/sites/2/2020/08/C307_SFRI_Zenix-2200.jpg1001503wmediahttps://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png3wmedia2020-08-26 09:19:532021-01-08 11:28:58Automated random access analyser
Two new Anti-Hepatitis E Virus (HEV) ELISAs provide reliable detection of HEVspecific antibodies of class IgG and IgM. The IgG ELISA is, moreover, the only commercial HEV ELISA to provide quantification in international units (IU/ml). The assay is calibrated according to the WHO reference serum and shows first-rate linearity with respect to this standard. The ELISA microplates are coated with highly purified recombinant HEV structural proteins, which ensure high sensitivity and specificity in antibody detection. The Anti-HEV ELISAs are ideal for differential diagnosis, for epidemiological studies and, in combination with PCR, for blood donor screening. The tests are easy to perform and can be fully automated on microplate processing systems such as the company’s Analyzer series. Infections with HEV are the most frequent cause on non-A, non-B hepatitis worldwide. They are generally acquired fecal-orally via contaminated drinking water or food (e.g. insufficiently cooked pork). HEV is endemic primarily in countries with low standards of hygiene, but is also increasingly observed in industrialized nations. HEV infections generally take a mild course, but in rare cases they can lead to acute liver failure. Prognosis is particularly poor in pregnant women, and in this group the mortality rate reaches up to 20%. Since an HEV infection resembles hepatitis A and other hepatides in the preliminary stages, differential diagnostic tests as part of the clinical and laboratory investigation are essential. Alongside PCR analysis of viral RNA in blood or stool, the serological detection of HEV-specific IgM and IgG antibodies plays a decisive role in acute HEV diagnostics. Read more
A new generic chemistry reagent line, packaged in a bar-coded bottle, allows easy application to the Beckman Coulter AUTM 400/480/640 chemistry analysers. This direct-placement packaging reduces both technician time and the potential for costly errors, while providing greater operator convenience and ease-of-use by enabling automated on-board reagent management. This line also has the potential to offer significant cost savings over the instrument manufacturer’s branded reagents. The liquid stable formulations show excellent accuracy and precision. Available products in this line include reagents to perform BMP’s, CMP’s, Lipid Panels, Renal Panels, Hepatic Panels, and other general chemistry tests. Read more
https://clinlabint.com/wp-content/uploads/sites/2/2020/08/C295_PointeSci_PI-O1111-01.jpg1061503wmediahttps://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png3wmedia2020-08-26 09:19:532021-01-08 11:28:58Bar-coded chemistry reagent line
Bio/Data Corporation is now offering a Tele-Check✓™ Calibration Verification Service for its platelet aggregometers. This calibration verification is performed over the phone while the aggregometer remains in the laboratory and is available for the PAP-8E and PAP-4 Series aggregometers in good working order. This service reduces downtime, save costs, and assures the platelet aggregometer is performing to published specifications. A service technician guides the user through the calibration verification process. Required materials are shipped to the laboratory in advance of the scheduled Tele-Check appointment. Calibration results generated by the instrument are submitted by the laboratory to the company for review by a Quality Control representative. Upon approval, a Certificate of Calibration will be issued along with a Calibration Sticker. Read more
https://clinlabint.com/wp-content/uploads/sites/2/2020/08/C297_BioDataCorp.jpg1501003wmediahttps://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png3wmedia2020-08-26 09:19:532021-01-08 11:28:58Calibration verification service for platelet aggregation testing
Helicobacter pylori (H. pylori) is a cork-screw-spiral-like gram-negative bacterium that has adapted to grow in the human stomach. The prevalence of H. pylori infection worldwide is approximately 66%, and in developing countries, it is as high as 80% – 90%. The testing and treatment of H. pylori is very important as it has been estimated that up to 20% of people infected with H. pylori will develop ulcers which may lead to specific cancers. MP Diagnostics ASSURE H. pylori Rapid Test and Helico Blot 2.1 Western Blot incorporate a unique marker, CIM, which is used to detect the current infection of H. pylori bacteria. CIM stands for Current Infection Marker which is actually a H. pylori-specific protein. The nucleotide sequence of the CIM antigen is homologous to a conserved secreted protein. This protein has been found to be highly immunogenic for detection of H. pylori infected patients with high Positive Predictive Value of >90%. It has been coined as Current Infection Marker because IgG antibodies for CIM have been found in patients with active H. pylori infection. These patients are confirmed to have active H. pylori infection by two or more active infection diagnostic tests such as rapid urease test, culture, histology, and Urea Breath Test. With CIM-based products, no additional tests are needed for detecting current H. pylori infection. Read more
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Rapid, simultaneous detection of respiratory pathogens
The Respiratory Multiplex Array is intended for the simultaneous detection of 22 bacterial and viral respiratory pathogens in individuals suspected of Respiratory Tract Infections. The ability to simultaneously detect these in one sample provides clinicians with a complete patient profile, enabling faster and more appropriate treatment decisions.
The Respiratory Multiplex Array is based on a combination of multiplex PCR, biochip hybridization and chemiluminescence detection using the Evidence Investigator analyser. The array can run 54 samples simultaneously in five hours. Identifying multiple pathogens will provide a rapid and more cost-effective diagnostic tool than current methods – which only look for single pathogens – thus reducing the time from presentation to treatment and minimizing sample requirements. Save time and costs associated with single pathogen detection by using the Respiratory Multiplex Array.
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Touch interface software for bench top chemistry systems
, /in Product News /by 3wmediaThe Selectra Touch Pro Software for the Selectra Pro S and Pro M Clinical Chemistry Systems provides touch screen operation with intuitive design and significantly boosts laboratory productivity, reduces errors and offers detailed traceability of results. The smart colour icons guide the operator through the daily operation with minimum effort. Auto validation with 40 laboratory configurable criteria speeds results as qualified test results are sent directly to the LIS and operators can focus on exceptions. Real time individual data are traceable and archived for each result including operator, QC, calibration, control, absorbance, and reagent lot expiration. Reagents, test parameters, calibration and control values are programmed automatically via barcode with inventory tracked in real time. Maintenance tasks are automated, tracked and set up to run when the analyser is not in use. Automated and customizable start and end of day checklists ensure all essential tasks are completed. Remote access diagnostics provide real time support, helping to decrease both downtime and costs. Interactive learning through a dedicated online training website includes maintenance modules to assist operators at all times.
Read more
Plastic serological pipettes
, /in Product News /by 3wmediaGlobe Scientific’s Uniplast™ plastic serological pipettes feature a onepiece construction designed to eliminate the risk of breakage and sample retention. Clear black graduation marks prevent ambiguity and guarantee precise liquid reading and >98% accuracy. The serological pipettes are produced from crystal clear virgin polystyrene (PS) and are colour coded for easy volume identification. The calibration of the pipettes is certified for accuracy. Each pipette has a bonded polyolefin aerosol barrier plug to prevent pipettor contamination. The specially designed tip provides the best fill and release rates. Sterile pipettes are RNase-free, DNase-free, non-pyrogenic, non-hemolytic and non-cytotoxic. Manufactured under strict ISO 9001:2008 quality standards. they are available in 1mL, 2mL, 5mL, 10mL and 25mL sizes.
Read more
New fertility biochemistry control
, /in Product News /by 3wmediaExpanding Bio- Systems’ fertility line portfolio, the Fertility Biochemistry Control is a lyophilized control (1 mL) containing component concentration suitable for the quality control of fertility testing in clinical laboratories: Citrate, Fructose and Zinc. This new product complements the company’s line for laboratories dedicated to fertility control.
Read more
Human MxA Protein ELISA
, /in Product News /by 3wmediaDesigned for the measurement of MxA protein in human whole blood, an innovative ELISA based on the use of patented monoclonal antibodies and a special buffer to extract the cytoplasmic MxA protein is suitable for the monitoring of IFN-β therapy in multiple sclerosis patients and for viral infection recognition. Human Myxovirus protein A is induced exclusively by IFN-α and IFN-β. Since direct measurement of the IFN levels in plasma is difficult, MxA may be useful as a marker distinguishing viral disease from bacterial infection or from acute graft-versus-host disease after allogenic stem cell transplantation. Neutralizing antibodies may develop during the IFN-β therapy of multiple sclerosis and lead to loss of drug bioactivity. The IFN-β-inducible MxA protein is an ideal marker of IFN-β bioavailability, capable of discriminating between biologically responsive and non-responsive patients. The BioVendor assay meets all the requirements for routine clinical use in manual mode as well as on open ELISA robotic systems.
Read more
Automated random access analyser
, /in Product News /by 3wmediaDesigned for daily use in small labs and providing all the qualities of a high throughput qualitative instrument at an affordable rate, the ZENIX 2200 features a high quality optical system, using semi-reflective mirrors and cuvettes with excellent UV penetrability for the same level of sensitivity as the best systems on the market. Efficiency is increased thanks to its independent washing station, 44 reagent and 44 sample capacity rotors and its comprehensive software compatible with Windows® 7, Vista and XP. With a throughput of 200 tests/hour, the instrument also uses automatic dilution and retesting when concentrations are outside limits. Its maintenance-free micro pump and easy access to internal systems optimize maintenance and allow for quick and easy servicing.
Read more
HEV ELISAs
, /in Product News /by 3wmediaTwo new Anti-Hepatitis E Virus (HEV) ELISAs provide reliable detection of HEVspecific antibodies of class IgG and IgM. The IgG ELISA is, moreover, the only commercial HEV ELISA to provide quantification in international units (IU/ml). The assay is calibrated according to the WHO reference serum and shows first-rate linearity with respect to this standard. The ELISA microplates are coated with highly purified recombinant HEV structural proteins, which ensure high sensitivity and specificity in antibody detection. The Anti-HEV ELISAs are ideal for differential diagnosis, for epidemiological studies and, in combination with PCR, for blood donor screening. The tests are easy to perform and can be fully automated on microplate processing systems such as the company’s Analyzer series. Infections with HEV are the most frequent cause on non-A, non-B hepatitis worldwide. They are generally acquired fecal-orally via contaminated drinking water or food (e.g. insufficiently cooked pork). HEV is endemic primarily in countries with low standards of hygiene, but is also increasingly observed in industrialized nations. HEV infections generally take a mild course, but in rare cases they can lead to acute liver failure. Prognosis is particularly poor in pregnant women, and in this group the mortality rate reaches up to 20%. Since an HEV infection resembles hepatitis A and other hepatides in the preliminary stages, differential diagnostic tests as part of the clinical and laboratory investigation are essential. Alongside PCR analysis of viral RNA in blood or stool, the serological detection of HEV-specific IgM and IgG antibodies plays a decisive role in acute HEV diagnostics.
Read more
Bar-coded chemistry reagent line
, /in Product News /by 3wmediaA new generic chemistry reagent line, packaged in a bar-coded bottle, allows easy application to the Beckman Coulter AUTM 400/480/640 chemistry analysers. This direct-placement packaging reduces both technician time and the potential for costly errors, while providing greater operator convenience and ease-of-use by enabling automated on-board reagent management. This line also has the potential to offer significant cost savings over the instrument manufacturer’s branded reagents. The liquid stable formulations show excellent accuracy and precision. Available products in this line include reagents to perform BMP’s, CMP’s, Lipid Panels, Renal Panels, Hepatic Panels, and other general chemistry tests.
Read more
Calibration verification service for platelet aggregation testing
, /in Product News /by 3wmediaBio/Data Corporation is now offering a Tele-Check✓™ Calibration Verification Service for its platelet aggregometers. This calibration verification is performed over the phone while the aggregometer remains in the laboratory and is available for the PAP-8E and PAP-4 Series aggregometers in good working order. This service reduces downtime, save costs, and assures the platelet aggregometer is performing to published specifications. A service technician guides the user through the calibration verification process. Required materials are shipped to the laboratory in advance of the scheduled Tele-Check appointment. Calibration results generated by the instrument are submitted by the laboratory to the company for review by a Quality Control representative. Upon approval, a Certificate of Calibration will be issued along with a Calibration Sticker.
Read more
H. pylori rapid test
, /in Product News /by 3wmediaHelicobacter pylori (H. pylori) is a cork-screw-spiral-like gram-negative bacterium that has adapted to grow in the human stomach. The prevalence of H. pylori infection worldwide is approximately 66%, and in developing countries, it is as high as 80% – 90%. The testing and treatment of H. pylori is very important as it has been estimated that up to 20% of people infected with H. pylori will develop ulcers which may lead to specific cancers. MP Diagnostics ASSURE H. pylori Rapid Test and Helico Blot 2.1 Western Blot incorporate a unique marker, CIM, which is used to detect the current infection of H. pylori bacteria. CIM stands for Current Infection Marker which is actually a H. pylori-specific protein. The nucleotide sequence of the CIM antigen is homologous to a conserved secreted protein. This protein has been found to be highly immunogenic for detection of H. pylori infected patients with high Positive Predictive Value of >90%. It has been coined as Current Infection Marker because IgG antibodies for CIM have been found in patients with active H. pylori infection. These patients are confirmed to have active H. pylori infection by two or more active infection diagnostic tests such as rapid urease test, culture, histology, and Urea Breath Test. With CIM-based products, no additional tests are needed for detecting current H. pylori infection.
Read more
Respiratory Multiplex Array
, /in Product News /by 3wmediaRapid, simultaneous detection of respiratory pathogens
The Respiratory Multiplex Array is intended for the simultaneous detection of 22 bacterial and viral respiratory pathogens in individuals suspected of Respiratory Tract Infections. The ability to simultaneously detect these in one sample provides clinicians with a complete patient profile, enabling faster and more appropriate treatment decisions.
The Respiratory Multiplex Array is based on a combination of multiplex PCR, biochip hybridization and chemiluminescence detection using the Evidence Investigator analyser. The array can run 54 samples simultaneously in five hours. Identifying multiple pathogens will provide a rapid and more cost-effective diagnostic tool than current methods – which only look for single pathogens – thus reducing the time from presentation to treatment and minimizing sample requirements. Save time and costs associated with single pathogen detection by using the Respiratory Multiplex Array.
Website: http://www.randox.com/respiratory-molecular-test.php
Email: marketing@randox.com
Read more