BioChromato

BioChromato introduces sterile 96-well plate seal for cell culturing

BioChromato has introduced a gamma sterilized version of its popular RAPID Slit Seal for scientists looking to eliminate solvent evaporation from samples when culturing cells in 96-well microplates.
The RAPID Slit Seal is a proprietary self-closing microplate seal that returns to its original state even when punched with an HPLC or LC/MS autosampler. As a result, loss of volatile solvents from samples is eliminated.
In addition, with RAPID Slit Seal, insertion of pipette tips and sampling needles is easier and can be achieved without dragging.
In addition, with RAPID Slit Seal, insertion of pipette tips and sampling needles is easier and can be achieved without dragging.

  • For further information, visit: www.bicr.biz/product/consumables/rapid-slit-seal

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cytosmart Organoid Counting software

CytoSMART Technologies introduces automated organoid counter

CytoSMART Technologies has launched an automated organoid counter. The software application detects organoids using bright-field image analysis and runs on the Corning Cell Counter, a CytoSMART product.
Manually counting organoids is a routine part of laboratory operations, but is time consuming and user dependent. To overcome these issues CytoSMART has introduced this organoid counting application.
Joffry Maltha, CEO at CytoSMART Technologies, explained: “The 3D cellular structures that are formed in organoids have great potential in drug discovery and developmental biology. This has fuelled the ever-growing interest in culturing new sub-types of organoids and optimization of current protocols. Growing organoids does however take a substantial amount of time and skill. We believe that implementation of an automated solution for organoid counting can really speed up day-to-day work in the lab and is a logical step towards further implementation of organoids in cell culture-based research.”
The main features of the CytoSMART Organoid Counter are:

  • The main features of the CytoSMART Organoid Counter are:
  • Low-cost – works with a common reusable glass hemocytometer. No consumables required.
  • Precise – software allows for data gating and image selection for statistical analysis.
  • For more information, visit: https://cytosmart.com/products/organoid-counting

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fujirebio Lumipulse

Fujirebio Europe receives CE mark for automated Lumipulse G SARS-CoV-2 antigen assay and ESPLINE SARS-CoV-2 rapid antigen device

Fujirebio Europe has received CE marking for their Lumipulse G SARS-CoV-2 Ag, a high-sensitivity antigen test for the fully automated CLEIA (chemiluminescent enzyme immunoassay) Lumipulse G system, and of the ESPLINE SARS-CoV-2 rapid antigen test. Fujirebio is a global leader in the field of high-quality in vitro diagnostics (IVD) testing.
The Lumipulse G series are robust, fully automated CLEIA immunoassay instruments. The Lumipulse G1200 and G600II have a throughput of respectively 120 and 60 tests per hour and allow laboratory personnel to randomly load samples as needed. CLEIA technology and automated testing provides increased sensitivity, reproducibility and throughput.
The ESPLINE SARS-CoV-2 is an immunochromatographic rapid antigen test, and unlike other nucleic acid-based tests on the IVD market that also detect the SARS-CoV-2 gene with high sensitivity, the ESPLINE test does not require any special equipment. It is a cassette-style assay using a simple procedure, and it has a short reaction time of 30 min.
Both assays received Japanese regulatory approval in May and June 2020 for use with nasopharyngeal and saliva samples (Lumipulse only) as an aid in the diagnosis of SARS-CoV-2 infection.
“We are the first company to develop and provide a fully automated SARS-CoV-2 antigen testing solution, to be used on our Lumipulse G series, together with a rapid test device on the ESPLINE platform, and expect these innovations will have a positive impact on result turnaround times and laboratory throughput of COVID-19 testing,” said Christiaan De Wilde, CEO at Fujirebio Europe.

  • For more information, visit: www.fujirebio.com/en/products-solutions/lumipulser-g-sarscov2-ag

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terry pizzie

Horizon Discovery introduces single cell RNAseq-linked CRISPR screening service

Horizon Discovery Group, a leader in the application of gene editing and gene modulation for cell line engineering, has added single cell RNAseq-linked pooled CRISPR screening to its CRISPR screening services portfolio. The platform offers high-quality screening data and biological insight to address critical gaps in target identification and validation.
This launch is the result of a collaboration, announced in 2018, to develop and apply this novel research tool to discover new biology essential for the development of future therapeutics. The biological insight gained from Horizon’s single cell RNAseq-linked CRISPR screening platform could help researchers gain further understanding into complex biological models and speed up the time from discovery to validation by integrating the effect of gene editing with complex gene expression mapping.
Horizon’s pooled format screens offer researchers access to highly robust whole-genome level analyses that yield quality data outputs. Currently, it can be challenging to adequately multiplex the data from these screens to evaluate complex biological phenomena occurring in a subset of edited cells. Coupling pooled CRISPR screening to single cell RNAseq allows the impact of CRISPR-based gene modification to be examined on a global transcriptomic scale at single cell resolution. This could enable scientists to address critical gaps in target identification and validation as they work to develop new and more effective therapeutics.
Terry Pizzie, Chief Executive Officer, Horizon Discovery, explained: “Pooled CRISPR-Cas9 knockout screens have become a linchpin in drug target identification and validation. The development of our single cell RNAseq-linked pooled CRISPR screening service provides a substantial advance to Horizon’s screening capabilities. Our continuing development of cutting-edge services, including CRISPR screens in primary human immune cells, means we can offer our customers unparalleled insights into the biology that will help to underpin future drug and cell-based therapeutics.”

    For more information, visit: https://horizondiscovery.com/en/navigation/screening/functional-genomic-screening

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thermo fisher

Thermo Fisher’s new deployment model optimises LIMS implementation in Amazon Web Services cloud

Thermo Fisher Scientific has expanded deployment model options for SampleManager LIMS software, offering laboratories end-to-end support of the software deployment in the Amazon Web Services (AWS) Cloud.
Under a contract agreement, Thermo Fisher will manage the entire deployment process from installation and maintenance to backup and recovery. As a result, laboratories will benefit from significantly reduced financial and human resource investment associated with setting-up, running and maintaining traditional on-premise deployments or deployments to their own cloud hosting service.
At the same time, laboratories will retain control over the software upgrades and validation schedule, while taking advantage of unlimited and secure access to data from anywhere at any time, which will drive well-informed decision making and easier cross-collaboration. Furthermore, AWS Cloud deployment will enable unparalleled levels of scalability, with the LIMS expanding to meet evolving business needs.
Richard Milne, vice president and general manager of Digital Science, said: “Life science and industrial laboratories are increasingly adopting a cloud-first approach to enterprise-wide LIMS implementation. However, managing deployments to a laboratory’s own cloud hosting service can be a costly and resource-intensive process. We have developed the new cloud services to alleviate this burden and enable SampleManager LIMS software customers to use the system’s superior functionality and integration capabilities without having to invest significant resources into the setup and ongoing management of a cloud environment.”
The Cloud Services offering has been designed to provide optimal data security and protection. In addition to the security features available through standard AWS Cloud deployments, Thermo Fisher also implements its own robust Corporate Information Security (CIS) program, which outlines additional measures in line with security-by-design principles to maintain the confidentiality and integrity of data.

  • For more information, visit: www.thermofisher.com

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7 PRODUCT ELITECHGROUP

ELITechGroup Molecular Diagnostics distributes 3.5 million SARS-CoV-2 tests

ELITechGroup Molecular Diagnostics, a leading global provider of diagnostic testing products, passed a significant milestone early August with the distribution of more than 3.5 million SARS-CoV-2 tests worldwide. The company has also installed more than 500 of its lead diagnostics instrument, the ELITe InGenius polymerase chain reaction (PCR) system, globally, with over a hundred placed since the beginning of the pandemic. The system allows laboratories to reliably detect SARS-CoV2 in only a few hours, as well as conducting parallel testing for other diseases, such as flu, in order to ensure a correct diagnosis.
The ELITe InGenius has been widely used in hospitals and other healthcare settings since 2016, and ELITechGroup was among the first companies to have SARS-CoV-2 tests on a sample-to-result system.
The ELITe InGenius is a fully automated solution that can process 12 samples in parallel to deliver results in less than 2.5 hours. This brings several benefits over centralized high-throughput testing approaches as there is no waiting for a large batch of samples to accumulate before testing, and no delays from sending samples off premises to a central laboratory.
By performing extraction, amplification and result interpretation in one device, the ELITe InGenius replaces the multiple devices needed to perform such tasks separately. Full automation also means there is no need for constant supervision, allowing laboratory staff to perform other valuable work. More importantly, the limited hands-on time helps reduce the risk of infection for users. The instrument is straightforward to use, with only minimal training required from ELITechGroup’s service and support team.
The ELITe InGenius offers the widest molecular diagnostics menu available on a sample-to-result system, with 38 CE-IVD assays dedicated to the unique needs of healthcare settings, be it immunocompromised patient monitoring; detection of respiratory, gastro-intestinal, sexually transmitted or nosocomial infections; meningitis and encephalitis, as well as diagnostics of genetic factors.
Commenting on the advantages of the ELITe InGenius for hospital settings, Dr Anna Paola Callegaro, Virology Area Coordinator and Biobank UOSD Director of ASST Papa Giovanni XXIII – Bergamo (Italy), commented: “The modular configuration of the ELITe InGenius system enables us to carry out molecular virology routine with results on the day. The sample-to-result solution reduces the need for manual intervention by the technician and allows the analysis of multiple viral targets on the same sample, thereby significantly improving the lab’s efficiency.”
Christoph Gaue, ELITechGroup CEO, said the company has expanded their manufacturing capacity to help provide additional ELITe InGenius systems to hospitals and laboratories, globally.
For more information, visit: www.elitechgroup.com
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EUROIMMUN’s test detects SARS-CoV-2 antibodies from dried blood spots

Anti-SARS-CoV-2 antibodies can be determined quickly and efficiently in capillary blood (dried blood spots) using the CE-marked test and automation systems from EUROIMMUN.
The Blood Collection Set enables fast and convenient collection of blood from the fingertip by patients or healthcare professionals. The card containing the dried blood spots is then sent to a diagnostic lab without the need for cooling.
For the serological analysis EUROIMMUN exclusively offers two ELISAs for detection of IgG antibodies against the spike protein S1 domain or against modified nucleocapsid protein (NCP). The S1 antigen includes the immunologically relevant receptor binding domain, which is a key target of neutralisation antibodies.
Results obtained with the S1-based ELISA correlate well with those of neutralisation tests. NCP is the most immunodominant antigen of coronaviruses. The antigen used in the ELISA has been modified to contain only the diagnostically relevant epitopes, thus providing optimised performance.
The S1- and NCP-based IgG ELISAs demonstrate specificities of 99.6% and 99.8% and sensitivities of 94.4% and 94.6% respectively.
Parallel use of both ELISAs maximises the accuracy of SARS-CoV-2 antibody detection and can support determination of the SARS-CoV-2 antibody status before and after administration of future S1-based vaccines or antibody therapies.
The ELISAs can be processed automatically with high throughput on the EUROLab- Workstation ELISA. During processing the samples are clearly identified by means of barcodes ensuring a smooth traceable workflow. The dried blood spot analysis enriches EUROIMMUN’s portfolio for COVID-19 diagnostics, which also includes IgM and IgA ELISAs, as well as the EURORealTime SARS-CoV-2 for sensitive direct virus detection by PCR.
For more information, visit: www.coronavirus-diagnostics.com Read more

4 PRODUCT GREINER BIO ONE

Greiner Bio-One’s VeinViewer makes veins visible for venipuncture

Greiner Bio-One has launched their VeinViewer® which makes veins visible and helps to improve the success rate of an initial venipuncture. This significantly increases patient satisfaction and safety.
The VeinViewer uses harmless near-infrared (NIR) light which is directed towards the patient’s skin. Haemoglobin in the blood absorbs the NIR light and the surrounding tissue reflects it back to the VeinViewer device, where the data is processed into an image. Colour is added and the image is reflected on to the skin to provide a real time visualization of the blood vessels up to 10 mm below the skin.
High definition imaging technology helps provide clinicians with clear, sharp imaging which is particularly useful when vein visibility is poor.
Two VeinViewer devices are available. VeinViewer Flex is a portable device for use in emergency situations. It can also be made static by using the flexible arm to attach it to a table top or chair arm for example, which is useful when space is limited.
The VeinViewer Vision2 is a mobile imaging unit with an arm reaching up to 1.35 metres. It is attached to a trolley for easy transportation between beds or phlebotomy chairs.
For more information, visit: www.gbo.com
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1 PRODUCT AWARENESS TECHNOLOGY

Awareness Technology’s new analyser improves syphilis testing

Awareness Technology has recently introduced their ChemWell RPR Automated Nontreponemal analyser for the detection of syphilis. The company reports that it is the “most significant innovation to syphilis testing in the last 30 years”.
The analyser provides qualitative testing and screening for syphilis in human serum or plasma utilizing an advanced camera and software algorithm to analyse each sample.
In place of manual RPR cards, the system uses 4 standard 48-well microwell plates to analyse up to 192 samples per hour with no user intervention. High-resolution images captured by an advanced optical system are interpreted by a proven algorithm and provide an accurate and reliable negative or positive result based on the captured images.
An additional test can be run on positive samples to determine titers up to 1:2048 dilution for therapeutic monitoring. The software is included with the instrument at no additional cost and features an intuitive interface that allows for easy navigation and use.
Automated features such as fluid handling, mixing, timing, image capture, image processing, and reporting are all handled by the software.
Awareness Technology, with HQ in Palm City, Florida, US, develops, manufactures, and markets high quality in-vitro diagnostic instrumentation, and diagnostic test kits.
For more information, visit: www.awaretech.com
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6C PRODUCT TRIMERO

TRIMERO’s Free Light Chain assays CE marked for testing Kappa and Lambda FLC

TRIMERO’s new generation of Free Light Chain (FLC) assays, called KLoneus, includes an IVD CE marked assay for testing Kappa and Lambda FLC in non-concentrated urine samples on Siemens’ BN nephelometric systems.
The main features of the assays are:

  • particle enhanced nephelometric method
  • specifically developed to assay urine samples
  • based on polyclonal specific antibodies
  • with antigen excess control using the pre-reaction feature
  • values traced to the European Reference Material ERM-DA470k/IFCC (Institute for Reference Materials and Measurements, IRMM), in order to ensure consistent results and good correlation with other methods (urinary B&F Light Chain nephelometric assays, and BJP estimation by densitometry).

KLoneus FLC assays are also available for Beckman Coulter’s IMMAGE nephelometers and for the most popular clinical chemistry analysers. Other available assays for Siemens’ BN systems include: C1q Complement, C5 Complement, C3 pro-activator (Factor B) and IgD Immunoglobulins.
For more information, visit: www.3diag.com
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