Cancer Product List 4310 Rheinfelden Switzerland [email protected]

Total Page:16

File Type:pdf, Size:1020Kb

Cancer Product List 4310 Rheinfelden Switzerland Info@Milananalytica.Ch Please search your product with Ctrl + F MILAN Analytica AG Baslerstrasse 15 Cancer product list 4310 Rheinfelden Switzerland www.milananalytica.ch [email protected] Please ask for more information under [email protected] Article Product number Alpha-fetoprotein (AFP) human plasma 000338 Alpha-fetoprotein (AFP) human serum 000339 Breast cancer plasma 000742 Breast cancer serum 000743 Carbohydrate antigen 125 (CA-125) plasma 000472 Carbohydrate antigen 125 (CA-125) serum 000473 Carbohydrate antigen 15-3 (CA 15-3) plasma 000474 Carbohydrate antigen 15-3 (CA 15-3) serum 000475 Carbohydrate antigen 195 (CA 195) plasma 000476 Carbohydrate antigen 195 (CA 195) serum 000477 Carbohydrate antigen 19-9 (CA 19-9) plasma 000478 Carbohydrate antigen 19-9 (CA 19-9) serum 000479 Carbohydrate antigen 242 (CA 242) plasma 000480 Carbohydrate antigen 242 (CA 242) serum 000481 Carbohydrate antigen 27-29 (CA 27-29) plasma 000482 Carbohydrate antigen 27-29 (CA 27-29) serum 000483 Carbohydrate antigen 50 (CA 50) plasma 000484 Carbohydrate antigen 50 (CA 50) serum 000485 Carbohydrate antigen 549 (CA 549) plasma 000486 Carbohydrate antigen 549 (CA 549) serum 000487 Carbohydrate antigen 72-4 (CA 72-4) plasma 000488 Carbohydrate antigen 72-4 (CA 72-4) serum 000489 Carcinogenic embryonic antigen (CEA) plasma 000491 Carcinogenic embryonic antigen (CEA) serum 000490 Colorectal cancer plasma 000744 Colorectal cancer serum 000745 Free prostate-specific antigen (PSA) human plasma 000496 Free prostate-specific antigen (PSA) human serum 000497 HER2/new oncogen (human epidermal growth factor receptor) human plasma 000530 HER2/new oncogen (human epidermal growth factor receptor) human serum 000531 Human myeloma IgA plasma 000563 Human myeloma IgA serum 000564 MILAN Analytica AG [email protected] Baslerstrasse 15 Phone: +41 61 845 99 88 4310 Rheinfelden, Switzerland www.milananalytica.ch 1 / 2 Please search your product with Ctrl. + F Human myeloma IgE plasma, from cell culture 000567 Human myeloma IgE plasma, native 000566 Human myeloma IgE serum, from cell culture 000568 Human myeloma IgE serum, native 000565 Human myeloma IgG plasma 000570 Human myeloma IgG serum 000569 Human myeloma IgM plasma 000572 Human myeloma IgM serum 000571 Kidney cancer plasma 000754 Kidney cancer serum 000755 Liver cancer plasma 000752 Liver cancer serum 000753 Lung cancer plasma 000748 Lung cancer serum 000749 Multiple myeloma plasma 000870 Multiple myeloma serum 000871 NSE (neuron specific enolase) human plasma 000573 NSE (neuron specific enolase) human serum 000574 Ovarian cancer plasma 000740 Ovarian cancer serum 000741 PAP (prostate-specific acid phosphatase) human plasma 000575 PAP (prostate-specific acid phosphatase) human serum 000576 Prostate cancer plasma 000746 Prostate cancer serum 000747 Prostatic Acid Phosphatase (PAP) plasma 000782 Prostatic Acid Phosphatase (PAP) serum 000783 Random hospital specimens, plasma 000726 Random hospital specimens, serum 000727 Skin cancer plasma 000756 Skin cancer serum 000757 Small cell lung cancer (bronchial carcinoma) plasma 000750 Small cell lung cancer (bronchial carcinoma) serum 000751 Total PSA (prostate-specific antigen) human plasma 000581 Total PSA (prostate-specific antigen) human serum 000582 Tumor marker plasma 000332 Tumor marker serum 000333 MILAN Analytica AG [email protected] Baslerstrasse 15 Phone: +41 61 845 99 88 4310 Rheinfelden, Switzerland www.milananalytica.ch 2 / 2.
Recommended publications
  • Novel Diagnostic and Predictive Biomarkers in Pancreatic Adenocarcinoma
    Review Novel Diagnostic and Predictive Biomarkers in Pancreatic Adenocarcinoma John C. Chang 1,* and Madappa Kundranda 2 1 Division of Radiology, Banner MD Anderson Cancer Center, Gilbert, AZ 85234, USA 2 Division of Medical Oncology, Banner MD Anderson Cancer Center, Gilbert, AZ 85234, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-480-256-3334 Academic Editor: Srikumar Chellappan Received: 23 January 2017; Accepted: 10 March 2017; Published: 20 March 2017 Abstract: Pancreatic ductal adenocarcinoma (PDAC) is a highly lethal disease for a multitude of reasons including very late diagnosis. This in part is due to the lack of understanding of the biological behavior of PDAC and the ineffective screening for this disease. Significant efforts have been dedicated to finding the appropriate serum and imaging biomarkers to help early detection and predict response to treatment of PDAC. Carbohydrate antigen 19-9 (CA 19-9) has been the most validated serum marker and has the highest positive predictive value as a stand-alone marker. When combined with carcinoembryonic antigen (CEA) and carbohydrate antigen 125 (CA 125), CA 19-9 can help predict the outcome of patients to surgery and chemotherapy. A slew of novel serum markers including multimarker panels as well as genetic and epigenetic materials have potential for early detection of pancreatic cancer, although these remain to be validated in larger trials. Imaging studies may not correlate with elevated serum markers. Critical features for determining PDAC include the presence of a mass, dilated pancreatic duct, and a duct cut-off sign. Features that are indicative of early metastasis includes neurovascular bundle involvement, duodenal invasion, and greater post contrast enhancement.
    [Show full text]
  • POTENTIAL ROLE of MUC1 by Dahlia M. Besmer a Dissertatio
    THE DEVELOPMENT OF NOVEL THERAPEUTICS IN PANCREATIC AND BREAST CANCERS: POTENTIAL ROLE OF MUC1 by Dahlia M. Besmer A dissertation submitted to the faculty of The University of North Carolina at Charlotte in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Biology Charlotte 2013 Approved by: _____________________________ Dr. Pinku Mukherjee _____________________________ Dr. Valery Grdzelishvili _____________________________ Dr. Mark Clemens _____________________________ Dr. Didier Dréau _____________________________ Dr. Craig Ogle ii © 2013 Dahlia M. Besmer ALL RIGHTS RESERVED iii ABSTRACT DAHLIA MARIE BESMER. Development of novel therapeutics in pancreatic and breast cancers: potential role of MUC1. (Under the direction of DR. PINKU MUKHERJEE) Pancreatic ductal adenocarcinoma (PDA) is the 4th leading cause of cancer-related deaths in the US, and breast cancer (BC) contributes to ~40,000 deaths annually. The development of novel therapeutic agents for improving patient outcome is of paramount importance. Importantly, MUC1 is a mucin glycoprotein expressed on the apical surface of normal glandular epithelia but is over expressed and aberrantly glycosylated in >80% of human PDA and in >90% of BC. In the present study, we first utilize a model of PDA that is Muc1-null in order to elucidate the oncogenic role of MUC1. We show that lack of Muc1 significantly decreased proliferation, invasion, and mitotic rates both in vivo and in vitro. Next, we evaluated the anticancer efficacy of oncolytic virus (OV) therapy that utilizes viruses to kill tumor cells. The oncolytic potential of vesicular stomatitis virus (VSV) was analyzed in a panel of human PDA cell lines in vitro and in vivo in immune compromised mice.
    [Show full text]
  • Serum Protein Fingerprinting by PEA Immunoassay Coupled with a Pattern-Recognition Algorithms Distinguishes MGUS and Multiple Myeloma
    www.impactjournals.com/oncotarget/ Oncotarget, 2017, Vol. 8, (No. 41), pp: 69408-69421 Research Paper Serum protein fingerprinting by PEA immunoassay coupled with a pattern-recognition algorithms distinguishes MGUS and multiple myeloma Petra Schneiderova1,*, Tomas Pika2,*, Petr Gajdos3, Regina Fillerova1, Pavel Kromer3, Milos Kudelka3, Jiri Minarik2, Tomas Papajik2, Vlastimil Scudla2 and Eva Kriegova1 1Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic 2Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University and University Hospital, Olomouc, Czech Republic 3Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VSB-Technical University of Ostrava, Ostrava, Czech Republic *These authors have contributed equally to this work Correspondence to: Eva Kriegova, email: [email protected] Keywords: serum pattern, cytokines, growth factors, proximity extension immunoassay, post-transplant serum pattern Received: May 04, 2016 Accepted: July 28, 2016 Published: August 12, 2016 Copyright: Schneiderova et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. ABSTRACT Serum protein fingerprints associated with MGUS and MM and their changes in MM after autologous stem cell transplantation (MM-ASCT, day 100) remain unexplored. Using highly-sensitive Proximity Extension ImmunoAssay on 92 cancer biomarkers (Proseek Multiplex, Olink), enhanced serum levels of Adrenomedullin (ADM, Pcorr= .0004), Growth differentiation factor 15 (GDF15, Pcorr= .003), and soluble Major histocompatibility complex class I-related chain A (sMICA, Pcorr= .023), all prosurvival and chemoprotective factors for myeloma cells, were detected in MM comparing to MGUS.
    [Show full text]
  • Molecular and Clinical Markers of Pancreas Cancer
    JOP. J Pancreas (Online) 2010 Nov 9; 11(6):536-544. EDITORIAL Molecular and Clinical Markers of Pancreas Cancer James L Buxbaum1, Mohamad A Eloubeidi2 1Divisions of Gastroenterology and Hepatology, University of Southern California. Los Angeles, CA, USA. 2University of Alabama in Birmingham. Birmingham, AL, USA Summary Pancreas cancer has the worst prognosis of any solid tumor but is potentially treatable if it is diagnosed at an early stage. Thus there is critical interest in delineating clinical and molecular markers of incipient disease. The currently available biomarker, CA 19-9, has an inadequate sensitivity and specificity to achieve this objective. Diabetes mellitus, tobacco use, and chronic pancreatitis are associated with pancreas cancer. However, screening is currently only recommended in those with hereditary pancreatitis and genetic syndromes which predispose to cancer. Ongoing work to identify early markers of pancreas cancer consists of high throughput discovery methods including gene arrays and proteomics as well as hypothesis driven methods. While several promising candidates have been identified none has yet been convincingly proven to be better than CA 19-9. New methods including endoscopic ultrasound are improving detection of pancreas cancer and are being used to acquire tissue for biomarker discovery. Pancreas cancer has the darkest prognosis of any poor screening test. At the Samsung Medical Center in gastrointestinal cancer with the mortality approaching South Korea 70,940 asymptomatic patients were the incidence [1]. While the overall five year survival screened using CA 19-9. However, among 1,063 with is less than 4%, those recognized early, with tumor elevated levels only 4 had pancreas cancer and only 2 involving only the pancreas have a 25-30% five-year had resectable disease [6].
    [Show full text]
  • Blood Markers for Early Detection of Colorectal Cancer: a Systematic Review
    1935 Review Blood Markers for Early Detection of Colorectal Cancer: A Systematic Review Sabrina Hundt, Ulrike Haug, and Hermann Brenner Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Bergheimer Strasse 20, Heidelberg, Germany Abstract Background: Despite different available methods for protein markers, but DNA markers and RNA colorectal cancer (CRC) screening and their proven markers were also investigated. Performance char- benefits, morbidity, and mortality of this malignancy are acteristics varied widely between different markers, still high, partly due to lowcompliance with screening. but also between different studies using the same Minimally invasive tests based on the analysis of blood marker. Promising results were reported for some specimens may overcome this problem. The purpose novel assays, e.g., assays based on SELDI-TOF MS of this reviewwas to give an overviewof published or MALDI-TOF MS, for some proteins (e.g., soluble studies on blood markers aimed at the early detection of CD26 and bone sialoprotein) and also for some CRC and to summarize their performance characteristics. genetic assays (e.g., L6 mRNA), but evidence thus Method: The PUBMED database was searched for far is restricted to single studies with limited relevant studies published until June 2006. Only studies sample size and without further external valida- with more than 20 cases and more than 20 controls were tion. included. Information on the markers under study, on Conclusions: Larger prospective studies using study the underlying study populations, and on performance populations representing a screening population are characteristics was extracted. Special attention was needed to verify promising results. In addition, future given to performance characteristics by tumor stage.
    [Show full text]
  • In Digestive Tract Diseases
    Br. J. Cancer 636-640 Macmillan Press Ltd., 1991 Br. J. Cancer (1991), 63, 636-640 ©%.J-'." Macmillan Press Ltd., Comparison of a new tumour marker CA 242 with CA 19-9, CA 50 and carcinoembryonic antigen (CEA) in digestive tract diseases P. Kuusela', C. Haglund2 & P.J. Roberts2 'Department of Bacteriology and Immunology, University of Helsinki, Haartmaninkatu 3, SF-00290 Helsinki; and 2IV Department of Surgery, Helsinki University Central Hospital, Kasarminkatu 11-13, SF-00130 Helsinki, Finland. Summary The levels of CA 242, a new tumour marker of carbohydrate nature, were measured in sera of 185 patients with malignancies of the digestive tract and of 123 patients with benign digestive tract diseases. High percentages of elevated CA 242 levels (>20 U ml-') were recorded in patients with pancreatic and biliary cancers (68%). The sensitivity was somewhat lower than that of CA 19-9 (76%) and CA 50 (73%). On the other hand, in benign pancreactic and biliary tract diseases the CA 242 level was less frequently elevated than the CA 19-9 and CA 50 levels. The serum CA 242 concentration was increased in 55% of patients with colorectal cancer. CA 242 detected more Dukes A-B carcinomas (47%) than CEA (32%), whereas CEA was more often elevated (71% vs 59%) in Dukes C-D carcinomas. CA 242 was slightly elevated (ad 41 U ml-') in 10% of patients with benign colorectal diseases. CA 50 and CA 19-9 had lower sensitivities than CA 242 using the recommended cut-off values. When cut-off levels based on relevant benign colorectal diseases were used, the sensitivities of these markers were similar and somewhat higher than that of CEA.
    [Show full text]
  • Use of Tumor Markers in Testicular, Prostate, Colorectal, Breast, and Ovarian Cancers Edited by Catharine M
    Laboratory Medicine Practice Guidelines Use of Tumor Markers in Testicular, Prostate, Colorectal, Breast, and Ovarian Cancers Edited by Catharine M. Sturgeon and Eleftherios Diamandis NACB_LMPG_Ca1cover.indd 1 11/23/09 1:36:03 PM Tumor Markers.qxd 6/22/10 7:51 PM Page i The National Academy of Clinical Biochemistry Presents LABORATORY MEDICINE PRACTICE GUIDELINES USE OF TUMOR MARKERS IN TESTICULAR, PROSTATE, COLORECTAL, BREAST, AND OVARIAN CANCERS EDITED BY Catharine M. Sturgeon Eleftherios P. Diamandis Copyright © 2009 The American Association for Clinical Chemistry Tumor Markers.qxd 6/22/10 7:51 PM Page ii National Academy of Clinical Biochemistry Presents LABORATORY MEDICINE PRACTICE GUIDELINES USE OF TUMOR MARKERS IN TESTICULAR, PROSTATE, COLORECTAL, BREAST, AND OVARIAN CANCERS EDITED BY Catharine M. Sturgeon Eleftherios P. Diamandis Catharine M. Sturgeon Robert C. Bast, Jr Department of Clinical Biochemistry, Department of Experimental Therapeutics, University of Royal Infirmary of Edinburgh, Texas M. D. Anderson Cancer Center, Houston, TX Edinburgh, UK Barry Dowell Michael J. Duffy Abbott Laboratories, Abbott Park, IL Department of Pathology and Laboratory Medicine, St Vincent’s University Hospital and UCD School of Francisco J. Esteva Medicine and Medical Science, Conway Institute of Departments of Breast Medical Oncology, Molecular Biomolecular and Biomedical Research, University and Cellular Oncology, University of Texas M. D. College Dublin, Dublin, Ireland Anderson Cancer Center, Houston, TX Ulf-Håkan Stenman Caj Haglund Department of Clinical Chemistry, Helsinki University Department of Surgery, Helsinki University Central Central Hospital, Helsinki, Finland Hospital, Helsinki, Finland Hans Lilja Nadia Harbeck Departments of Clinical Laboratories, Urology, and Frauenklinik der Technischen Universität München, Medicine, Memorial Sloan-Kettering Cancer Center, Klinikum rechts der Isar, Munich, Germany New York, NY 10021 Daniel F.
    [Show full text]
  • Evaluation of Serum CEA, CA19-9, CA72-4, CA125 And
    www.nature.com/scientificreports OPEN Evaluation of Serum CEA, CA19-9, CA72-4, CA125 and Ferritin as Diagnostic Markers and Factors of Received: 20 October 2017 Accepted: 26 January 2018 Clinical Parameters for Colorectal Published: xx xx xxxx Cancer Yanfeng Gao1, Jinping Wang2, Yue Zhou3, Sen Sheng4, Steven Y. Qian5 & Xiongwei Huo6 Blood-based protein biomarkers have recently shown as simpler diagnostic modalities for colorectal cancer, while their association with clinical pathological characteristics is largely unknown. In this study, we not only examined the sensitivity and reliability of single/multiple serum markers for diagnosis, but also assessed their connection with pathological parameters from a total of 279 colorectal cancer patients. Our study shown that glycoprotein carcinoembryonic antigen (CEA) owns the highest sensitivity among single marker in the order of CEA > cancer antigen 72-4 (CA72-4) > cancer antigen 19-9 9 (CA19-9) > ferritin > cancer antigen 125 (CA125), while the most sensitive combined-markers for two to fve were: CEA + CA72-4; CEA + CA72-4 + CA125; CEA + CA19-9 + CA72-4 + CA125; and CEA + CA19-9 + CA72-4 + CA125 + ferritin, respectively. We also demonstrated that patients who had positive preoperative serum CEA, CA19-9, or CA72-4 were more likely with lymph node invasion, positive CA125 were prone to have vascular invasion, and positive CEA or CA125 were correlated with perineural invasion. In addition, positive CA19-9, CA72-4, or CA125 was associated with poorly diferentiated tumor, while CEA, CA19-9, CA72-4, CA125 levels were positively correlated with pathological tumor-node-metastasis stages. We here conclude that combined serum markers can be used to not only diagnose colorectal cancer, but also appraise the tumor status for guiding treatment, evaluation of curative efect, and prognosis of patients.
    [Show full text]
  • A Novel Multiplexed Immunoassay Identifies CEA, IL-8 and Prolactin As
    Mahboob et al. Clinical Proteomics (2015) 12:10 DOI 10.1186/s12014-015-9081-x CLINICAL PROTEOMICS RESEARCH Open Access A novel multiplexed immunoassay identifies CEA, IL-8 and prolactin as prospective markers for Dukes’ stages A-D colorectal cancers Sadia Mahboob1, Seong Beom Ahn1, Harish R Cheruku1, David Cantor1, Emma Rennel3, Simon Fredriksson3, Gabriella Edfeldt3, Edmond J Breen4, Alamgir Khan4, Abidali Mohamedali2, Md Golam Muktadir5, Shoba Ranganathan2, Sock-Hwee Tan1, Edouard Nice6 and Mark S Baker1* Abstract Background: Current methods widely deployed for colorectal cancers (CRC) screening lack the necessary sensitivity and specificity required for population-based early disease detection. Cancer-specific protein biomarkers are thought to be produced either by the tumor itself or other tissues in response to the presence of cancers or associated conditions. Equally, known examples of cancer protein biomarkers (e.g., PSA, CA125, CA19-9, CEA, AFP) are frequently found in plasma at very low concentration (pg/mL-ng/mL). New sensitive and specific assays are therefore urgently required to detect the disease at an early stage when prognosis is good following surgical resection. This study was designed to meet the longstanding unmet clinical need for earlier CRC detection by measuring plasma candidate biomarkers of cancer onset and progression in a clinical stage-specific manner. EDTA plasma samples (1 μL) obtained from 75 patients with Dukes’ staged CRC or unaffected controls (age and sex matched with stringent inclusion/exclusion criteria) were assayed for expression of 92 human proteins employing the Proseek® Multiplex Oncology I proximity extension assay. An identical set of plasma samples were analyzed utilizing the Bio-Plex Pro™ human cytokine 27-plex immunoassay.
    [Show full text]
  • The Diagnostic Value of Extracellular Protein Kinase a (ECPKA) in Serum for Gastric and Colorectal Cancer
    3878 Original Article The diagnostic value of extracellular protein kinase A (ECPKA) in serum for gastric and colorectal cancer Yan Wu1, Yafang Li1, Junqiang Liu2, Mengjiao Chen1, Wei Li3, Yongchang Chen1, Min Xu2 1Department of Physiology, School of Medicine, Jiangsu University, Zhenjiang, China; 2Department of Gastroenterology, Affiliated Hospital of Jiangsu University, Zhenjiang, China; 3The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China Contributions: (I) Conception and design: Y Wu; (II) Administrative support: Y Wu, M Xu; (III) Provision of study materials or patients: Y Wu, M Xu; (IV) Collection and assembly of data: J Liu, Y Li, M Chen, M Xu; (V) Data analysis and interpretation: Y Wu, W Li; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors. Correspondence to: Min Xu. Department of Gastroenterology, Affiliated Hospital of Jiangsu University, Zhenjiang, China. Email: [email protected]; Yan Wu. Department of Physiology, School of Medicine, Jiangsu University, 301 Xuefu, Zhenjiang, China. Email: [email protected]. Background: For the biomarkers of cancer, many chromosomal and genetic alterations have been examined as possible. However, some tumors do not display a clear molecular and genetic signature. While there are some cellular processes regulated by second messenger intracellular pathways indeed involved in carcinogenesis. The first intracellular second messenger was described as cyclic adenosine 3',5'-monophosphate (cAMP), and cAMP-dependent protein kinase (PKA) play a crucial role in several biological processes; The dysregulation of PKA-mediated signaling in several types of cancer should be investigated. More interesting, the alpha catalytic subunit of PKA (PKACα) could be secreted into the conditioned medium by different types of cancer cells, and it also existed in the serum of some cancer patients, defined as extracellular protein kinase A (ECPKA).
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 7,994,135 B2 Doronina Et Al
    US007994.135B2 (12) United States Patent (10) Patent No.: US 7,994,135 B2 Doronina et al. (45) Date of Patent: Aug. 9, 2011 (54) MONOMETHYLVALINE COMPOUNDS EE R 358, si al. CAPABLE OF CONUGATION TO LIGANDS 6,569,834W B1 5/2003 Pettitarter et et al. al. 6,620,911 B1 9, 2003 Pettit et al. (75) Inventors: Svetlana O. Doronina, Snohomish, WA 6,639,055 B1 10/2003 ETA. (US); Peter D. Senter, Seattle, WA (US); 6,884,869 B2 4/2005 Senter et al. Brian E. Toki, Shoreline, WA (US); 2.92. R. 39. sn' et al. Allen J. Ebens, San Carlos, CA (US), 7.553,816 B2 62009 senter et al. Toni Beth Kline, Seattle, WA (US); Paul 7,659,241 B2 2/2010 Senter et al. Polakis, Burlingame, CA (US); Mark X. 2S3, E: 23.9 E. et al. Sliwkowski, San ETR CA (US); 7,829,531- I B2 11/2010 Sentereng et al. Susan D. Spencer, Tiburon, CA (US) 7,837,980 B2 11/2010 Alley et al. 7.851,437 B2 12/2010 Senter et al. (73) Assignee: Seattle Genetics, Inc., Bothell, WA (US) 2002/0001587 A1 1/2002 Erickson et al. 2003/0083263 A1 5/2003 Doronina et al. (*) Notice: Subject to any disclaimer, the term of this 3.s: A. 3.3. She s al patent is extended or adjusted under 35 2004/0018194, A1 1/2004 Francisco et al. U.S.C. 154(b) by 812 days. 2004/0235068 A1 11/2004 Levinson 2005/OOO9751 A1 1/2005 Senter et al.
    [Show full text]
  • ELISA & Multiplexing
    Focus ELISA & Multiplexing AH diagnostics: Your Science – Our Focus Dedicated to helping life science and diagnostics laborato- Representing more than 35 suppliers, our portfolio covers ries perform their best by providing innovative, high quality your entire workflow from A to Z. products and expert knowledge. With offices in Copenhagen, Aarhus, Oslo, Stockholm and We offer the ultimate cutting edge technologies for ELISA, Helsinki, we serve the Nordic region with our 30 years of flow cytometry, imaging, pathology, protein analysis, qPCR, experience in the biotech field. single-cell analysis and bio appliance. Let Us Find the Right Solution for You The selection of ELISA kits is vast, and new ones are added each year. It can be confusing to find the right ELISA kit for your project, but we are here to guide you. Whether your priority is accuracy, time use, budget or another requirement, we can help you find the best ELISA kits for your project. 5,700 From coat-it-yourself to ready-to-use ELISA kits ELISA kits Among our ELISA kits, you will find ready-to-use, coat-it-yourself, pre-coated, high sensitivity, phospho, and IVD/CE-marked ELISA kits. The kits are, depending on the target, based on different technologies in order to obtain the best possible sensitivity. If we don’t have the ELISA kit you are looking for, we are happy to source the product Build Coat it Pre- 1 wash for you your own yourself coated only Let ELISA instruments do the monotonous work We have a wide selection of washers and readers from trusted brands such as BioTek and Grifols.
    [Show full text]