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Archive for category: Product News

Product News

logo integra biosciences

Pipette tips designed for Integra pipettes

, 26 August 2020/in Product News /by 3wmedia

INTEGRA Biosciences has developed its GripTip pipette tips range to overcome the problems associated with the use of universal pipette tips. Universal pipette tips require hammering on to stretch the tip, often resulting in a suboptimal fit that can lead to loose, leaking and falling off tips. GripTips are designed to offer a perfect fit on INTEGRA pipettes, effortlessly snapping onto the tip fittings with low attachment and ejection forces. This ensures that all tips are at the same height, guaranteeing perfect alignment and seal, even when performing side well touch-offs. They span a wide volume range – from 0.5 to 5000 µl – and are available in sterile,  non-sterile and filtered options. The portfolio also includes a number of specialty GripTips, such as low retention tips for recovering viscous solutions, wide bore tips for cellular applications, short tips for improved ergonomics and targeting of small wells, and extra long tips for improved access to tubes. This range is continuously being expanded to ensure that there are GripTips to meet the needs of every customer, for every application. The two latest tips include a 1250 µl short tip – perfect for ergonomically pipet-ting large volumes, by eliminating the need to hold the pipette high over the bench, reducing the risk of RSI – and a 300-µl long tip that, at 102 mm long, enables the user to easily reach the bottom of standard 100 ml tubes. To aid tip selection, INTEGRA has launched its GripTip selector, simply using filters to identify the most suitable tips for the required workflow in seconds.

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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/logo-integra_biosciences.jpg 170 600 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:44Pipette tips designed for Integra pipettes
C432 Abbott Alinity m

Infectious disease testing system and assays

, 26 August 2020/in Product News /by 3wmedia

Abbott has announced CE Mark for the Alinity m diagnostic system and assays that will allow laboratories to meet the growing demand for infectious disease testing by offering increased efficiency, speed and accuracy. This new technology will provide high flexibility in molecular diagnostic testing, allowing more tests to be done in shorter timeframes, while reducing the space and number of instruments needed to conduct large amounts of tests. The World Health Organization (WHO) reports that more than a billion people around the world are living with infectious diseases. For people living with infectious diseases, quick and accurate molecular test results are needed to help prevent the spread of communicable diseases globally. Advanced molecular testing also allows patients to be diagnosed correctly and then monitored for their response to treatment. Molecular laboratories are playing an increasingly important role in providing critical test results for infectious disease diagnosis. Alinity m will significantly improve the way these laboratories operate by letting staff run any sample at any time, without the need to group samples, allowing them to focus on giving physicians the information they need to make accurate, timely clinical decisions. Alinity m provides superior flexibility for lab staff and faster testing results for clinicians and patients.  Alinity m may also reduce the lab equipment footprint from four to six instruments down to one – decreasing the space requirements and hours spent learning and maintaining different instruments. Now available in countries that recognize CE Mark, Alinity m offers initial assays including virologic testing for human immunodeficiency virus type 1 (HIV-1), hepatitis B virus (HBV) and hepatitis C virus (HCV); sexual health-related testing for Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, and Mycoplasma genitalium or CT/NG/TV/MG panel; and high-risk human papillomavirus (HPV) testing. Local product availability may vary depending on geographic location.

ABBOTT
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amsbiopr271 01

AMSBIO introduces StemFit for Differentiation for human iPS and ES cells

, 26 August 2020/in Product News /by 3wmedia

AMSBIO has introduced StemFit for Differentiation – a new chemically defined and animal component-free formulation that enables unmatched differentiation of human Induced Pluripotent Stem (hiPS) and Embryonic Stem (hES) cells.
The unique chemically defined composition of StemFit for Differentiation minimizes lot-to-lot variation, enabling highly consistent cell differentiation. Free of animal- and human-derived components, StemFit for Differentiation can be used to eliminate the risk of immunogenic contamination.
Applications proven to benefit from StemFit for Differentiation include: lineage-specific (endodermal, mesodermal and ectodermal) differentiation where this new product is used to replace serum-free supplements, as well as spontaneous differentiation of hiPSCs to organoids via embryoid body formation.
Used in combination with StemFit Basic feeder-free medium with iMatrix-511 laminin as extracellular matrix, StemFit for Differentiation enables researchers to undertake clinical applications involving both expansion and differentiation of human Pluripotent Stem Cell-derived cells and tissues.
Supplied as a 5X concentrate, StemFit for Differentiation has been formulated for use with basal cell culture medium (e.g. DMEM, RPMI 1640, DMEM/F12 etc.) and a variety of different induction factors or cytokines (including Activin A and bFGF from AMSBIO).

  • For further information on StemFit for Differentiation, visit: www.amsbio.com/stemfit-for-differentiation

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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/amsbiopr271_01.jpg 808 808 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:29AMSBIO introduces StemFit for Differentiation for human iPS and ES cells
PRODUCT CLI MICROLUTE

Porvair Sciences sets a new standard for labs with Microlute Protein Precipitation Plate

, 26 August 2020/in Product News /by 3wmedia

Incorporating a novel dual hydrophobically treated matrix filter, Microlute Protein Precipitation Plate from Porvair Sciences sets a new standard for labs looking to remove interfering proteins from serum, plasma or whole blood samples prior to analysis by Liquid Chromatography / Mass Spectrometry (LC/MS). Biological samples commonly contain proteins that interfere with downstream applications such as LC/MS analysis. Microlute Protein Precipitation Plates (PPP) use the CRASH method, in which protein is denatured with acetonitrile and the flocculant filtered out, allowing 96 samples to be processed in parallel. Based on the industry standard MicroLute format, but without the chromatographic sorbent, protein ‘crashes’ out of solution and precipitates directly in each well when acetonitrile is added, thus solving all common problems associated with the CRASH technique of protein cleanup. The novel dual frit, hydrophobically treated matrix used by the Microlute PPP means that there is no ‘wetting out’ and leakage of sample before the application of vacuum. Due to its ease of use, high performance and reliability the Microlute PPP is commonly used as the protein precipitation plate of choice in many major pharmaceutical companies worldwide. Established in 1992, Porvair Sciences is one of the largest global manufacturers of ultra-clean microplates and top-quality microplate equipment for life science, synthetic chemistry and many other applications.
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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/PRODUCT_CLI_MICROLUTE.jpg 457 694 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:37Porvair Sciences sets a new standard for labs with Microlute Protein Precipitation Plate
CLI 190902 doc Image SAA

Serum Amyloid A (SAA), CE-IVD marked, turbidimetric assay

, 26 August 2020/in Product News /by 3wmedia

TRIMERO has added to its catalogue a new Serum Amyloid A, CE-IVD marked, particle-enhanced turbidimetric immunoassay. Applications are available for the most popular clinical chemistry analysers, and for IMMAGE® nephelometers of Beckman Coulter. In order to ensure lot to lot traceability, the assay has been standardized to the Serum Amyloid A (SAA) 1st International Standard (NIBSC code: 92/680) of the WHO (World Health Organization).

Other available assays for turbidimetry and nephelometry include:

KLoneus® Free Light Chains (FLC), IgD Immunoglobulins, Retinol Binding Protein (RBP) for serum and urine, Soluble Transferrin Receptor (sTfR), Hemopexin, Cystatin-C for serum and urine, A1-Microglobulin, B2-Microglobulin for serum and urine, Kappa and Lambda Light Chains for serum and urine, Complement C1q, Complement C5, Factor B (C3 Proactivator), C1 (Esterase) Inhibitor.   

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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/CLI_190902_doc_Image-SAA.jpg 440 720 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:47Serum Amyloid A (SAA), CE-IVD marked, turbidimetric assay

Ansh labs launches two new immunoassays for SARS-COV2

, 26 August 2020/in Corona News, Product News /by 3wmedia

Ansh labs has launched two new immunoassays, SARS-CoV2 IgG and IgM ELISAs, to assist in the fight against the Covid-19 pandemic.
Ansh Labs is releasing these two kits for sale in the United States under the provisions outlined in Section D of Policy for Diagnostic Tests for Coronavirus Disease-2019 during the Public Health Emergency. At the time of going to press, these tests were under review by the FDA for an Emergency Use Authorization.
IgM antibody is the first to be produced in response to viral proteins (antigens) and will be primarily detectable during the early onset of the disease. IgG antibodies are long-lasting and can persist in the bloodstream for many years after infection. This test has the advantage of detecting not only individuals with active infection (IgM), but also those who were previously exposed to the virus and may have subsequently developed immunity (IgG).
Testing for SARS-CoV2 antibodies can help in epidemiological surveillance about the spread of the virus and possible herd immunity. Ansh Labs’ SARS-CoV2 ELISAs are highly accurate with IgG ELISA offering 96% specificity and IgM ELISA offering 99% specificity.
For more information, visit: www.covid-diagnostics.com
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NEWS CLI PORVAIR

Porvair Sciences expands range of black microplates

, 26 August 2020/in Product News /by 3wmedia

Porvair Sciences has expanded its range of high quality, black microplates that minimise sample degradation by exposure to light, even over long storage periods.
Available in a choice of 48-, 96- and 384-well formats – the black plates are precisely manufactured to applicable ANSI / SLAS dimensions ensuring complete compatibility with almost all readers and automated equipment. Manufactured from polypropylene, the range of black microplates offer excellent heat and solvent resistant qualities. Using only ultra-pure grade polymer means that each black plate has near zero leachates ensuring long-term sample integrity. The black plates are supplied RNase / DNase free meaning they can be used to store the most sensitive biological samples. To prevent evaporation, hydration of DMSO solutions and to completely eliminate light from samples – Porvair Sciences additionally offers a selection of Absorb Max light blocking sealing films that may be applied to the top of the black plates. A split backing and edge cut-outs make positioning and applying the sealing film quick and simple. The light-blocking and absorbing properties of Porvair Sciences black microplates, used in conjunction with Absorb Max sealing films, provides a perfect combination for protecting light-sensitive assays or samples during storage.
For more information, visit: www.microplates.com/solid-bottom
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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/NEWS_CLI_PORVAIR.jpg 488 694 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:40Porvair Sciences expands range of black microplates
C435 EUROIMMUN ELISA microplate manuell

ELISA for urinary sCD163 measurement

, 26 August 2020/in Product News /by 3wmedia

Urinary soluble CD163 (sCD163) is a novel non-invasive marker of renal inflammation, and its determination supports early detection and monitoring of active glomerulonephritis (GN). Studies by experts in the field led by Prof. Mark Little (Trinity College, Dublin, Ireland) showed that significantly increased sCD163 levels in urine are present in up to 87% of patients with active ANCA-associated vasculitis (AAV) with renal involvement. In contrast, only slight increases are detected in AAV patients in remission, patients with acute kidney failure or sepsis, and patients with AAV without kidney involvement (O’Reilly et al. Am Soc Nephrol 27: 2906–2916, 2016). Furthermore, urinary sCD163 is elevated in patients with non-vasculitic forms of GN, especially in patients with lupus nephritis class IV (Endo et al. J Nephrol Dial Transplant. 31(12): 2023-2033, 2016).  sCD163 is a macrophage activation marker. The sCD163 level in urine correlates directly with the kidney disease activity, reflecting the accumulation of CD163+ macrophages in the glomeruli in response to pro-inflammatory stimuli. The direct correlation with renal inflammation means that urinary sCD163 is superior in performance to standard urinary markers, which have limited value in identifying a renal relapse. Monitoring of urinary sCD163 values can help to predict renal flares before irreversible kidney damage occurs and might enable invasive kidney biopsies to be avoided.  sCD163 can be measured quantitatively in urine samples using a new ELISA from EUROIMMUN. The detection is based on monoclonal anti-sCD163 antibodies. Values are determined by means of a simple cut-off-based interpretation using 6 calibrators. The EUROIMMUN sCD163 ELISA will soon be available as IVD CE-marked assay.

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https://clinlabint.com/wp-content/uploads/sites/2/2020/08/C435_EUROIMMUN_ELISA_microplate_manuell.jpg 603 800 3wmedia https://clinlabint.com/wp-content/uploads/sites/2/2020/06/clinlab-logo.png 3wmedia2020-08-26 09:16:522021-01-08 11:20:49ELISA for urinary sCD163 measurement
Horizon chosource TerryPizzie CEO

Horizon Discovery CHOSOURCE platform supports development of immunotherapy for autoimmune diseases

, 26 August 2020/in Product News /by 3wmedia

Horizon Discovery Group, a leader in the application of gene editing and gene modulation for cell line engineering, says its cGMP-compliant CHOSOURCE™ platform has played a key role in generating a stable cell line for the development of an immunotherapy for autoimmune diseases. Horizon’s pharmaceutical-grade, stable Chinese Hamster Ovary (CHO) cells delivered high yields of monoclonal antibody for LAG-3 immunotherapy, enabling Immutep and Batavia Biosciences to reach an important milestone in the preclinical development of the compound.
Horizon’s gene-edited Glutamine Synthetase (GS) knockout CHO K1 cell line expression system, offered by Batavia Biosciences as part of its STEP®-mAb service, was used to generate a high yielding cell line for Immutep’s IMP761 product candidate, an agonist antibody targeting the immune checkpoint lymphocyte activation gene (LAG)-3. LAG-3 controls the signalling between specific immune cells, T cells and antigen presenting cells, which are responsible for the adaptive immune response, making it a promising focus for novel cancer therapies or for the treatment of autoimmune conditions, such as inflammatory bowel diseases, rheumatoid arthritis, and multiple sclerosis.
Horizon’s GS expression system facilitates the development of stable cell lines for the expression of antibodies and other recombinant proteins and is recognized in the industry and by regulators as suitable for high yield biomanufacturing. Its CHOSOURCE biomanufacturing platform helps companies to move from the DNA sequence of their potential biotherapeutic to clinical manufacturing as simply and rapidly as possible. The platform is versatile and suitable for a broad range of monoclonal antibody therapeutics, delivering higher-than-anticipated yields of less commonly used IgG4-based antibodies, such as IMP761.
Terry Pizzie, CEO, Horizon Discovery said: “We are dedicated to ensuring availability of key technologies that can improve affordability of medicines worldwide. Our CHOSOURCE biomanufacturing platform is empowering organizations from early stage start-ups to large pharmaceutical companies to drive efficiencies throughout development and production and has already been utilized in multiple successful innovative new drug filings.”
The complete CHOSOURCE system includes the GS knockout CHO K1 cell line, a comprehensive package of supporting documentation, and an expression vector supplied under license from DNATwoPointO, Inc.
• For more information, visit: https://horizondiscovery.com/navigation/cho-cells
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Randox Reagents Webvertorial CLI November 2019 IMAGE

Randox diabetes testing portfolio

, 26 August 2020/in Product News /by 3wmedia

Type 2 diabetes mellitus (T2DM) now attains the status of global pandemic, spreading from developed to developing countries. The epidemiological trends indicate that the prevalence will continue to increase dramatically. The World Health Organization estimates diabetes to be the seventh global leading cause of death, accounting for 1.6 million deaths in 2016. Randox is committed to advancing diabetes testing, including the associated complications. Randox offers a comprehensive range of high quality reagents ranging from diabetes risk assessment, diagnosis and monitoring of diabetes, and monitoring of associated complications. The Randox diabetes portfolio covers the full spectrum of clinical biochemistry laboratory testing requirements including several superior performance and unique assays. Applications are available detailing instrument-specific settings for a wide range of clinical chemistry analysers. https://www.randox.com/diabetes-reagents/
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