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What Does In Vitro Diagnostic Use Mean? IVD products are known as "in vitro diagnostic products". IVD refers to medical devices, in vitro diagnostic reagents, and drugs. IVD, as a branch of medical devices, has unique definitions and regulatory supervision. The in vitro diagnostics industry and laboratory medicine constitute an organic whole that is not only different from each other but also closely related to each other. The in vitro diagnostics industry is the "tool" and "weapon" of laboratory medicine. At the same time, laboratory medicine is the "user" and "market" of the IVD industry. About 80% of clinical diagnosis information comes from IVD, and its cost accounts for less than 20% of medical expenses. IVD is an important part of diagnosis, Immunohistochemistry, treatment of human health. Medicament supplies ivd raw materials, in vitro diagnostics reagents and IVD test kits as well. Types Of IVD products list Neocide® IVD Reagents NeoCide® Preservative is effective preservation of chemicals (abbreviated to PC) and a new biocide (unison to NeoCide) for controlling microorganisms in biological media for professional in vitro diagnostic use only products. Neocide® Tris (hydroxymethyl) Aminomethane Good's buffer has the following characteristics: 1. High water solubility; 2. Low cell membrane permeability; 3. stable acid-base dissociation constant; 4. Low metal chelating capacity Cardiac Marker Test The main markers of myocardial injury were troponin T, troponin I, creatine kinase isoenzyme mass (CK MB) and myoglobin. Troponin is composed of three subunits. What are IVD products The full name of "IVD" is "in vitro diagnostic products". IVD refers to medical devices, in vitro diagnostic reagents and drugs. As a branch of medical devices, IVD has unique definitions and regulatory supervision. Advantages Of IVD Raw Materials Produced By Medikament We are committed to providing the highest quality ivd diagnostics raw materials and ivd diagnostics reagents for in vitro diagnostic use only. Our in vitro diagnostic products strictly control the quality inspection, which can provide you solid, repeatable, dependable results, to meet the critical challenges faced by reagent vendors, and the verification of government agencies. The ingredient of our ivd products is exactly the same as Sigma-Aldrich, Roche, et al. In Vitro Diagnostic Use Only Meaning The rapid development of IVD technology, from gene sequencing, SNP screening, point mutation gene diagnosis, to the detection of various biomarkers (biomarker) at the protein level, detection of circulating tumor cells (CTC) at the cellular level, thin layer Liquid-based cytology (TCT), then to PET/CT at the tissue level. The application prospects mainly include the following aspects: Physical examination, Chronic disease management, Critical illness monitoring. Frequently Asked Questions About IVD Raw Materials Q What Is IVD? A As we all know, the blood routine, urine routine, stool routine, blood sugar monitoring, anemia screening and so on that we do in the hospital all use diagnostic reagents. These diagnostic reagents are normally used without contact with the human body, so are they called "in vitro diagnostic reagents"? Nowadays, in-vitro diagnostic reagents are basically needed for disease prevention and clinical diagnosis and treatment. Whether it is the three major routine tests for hematuria and stool, the identification of viral and bacterial infections, the heart, liver, kidney, blood vessel, and immune function tests, in-vitro diagnostic reagents are inseparable. If you want to know more about in vitro diagnostics examples, please visit our website.

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Malaria Test Kit Malaria is a serious parasitic disease characterized by fever, chills, and anemia and is caused by a parasite that is transmitted from one human to another by the bite of infected Anopheles mosquitoes. Thereare four kinds of malaria that can infect humans: Plasmodium falciparum, P. vivax, P. ovale, and P. malariae. In humans, the parasites (called sporozoites) migrate to the liver where they mature and release another form, the merozoites. At the present, malaria is diagnosed by looking for theparasites in a drop of blood. Blood will be put onto a microscope slideand stained so that the parasites will be visible under a microscope.The Malaria pf/pv Test contains amembrane strip, which is pre-coated with two monoclonal antibodiesas two separate lines across a test strip. One monoclonal antibody (test line 1) is specific to the P. falciparum histidine rich protein-2 (Pf HRP-2) and another monoclonal antibody (test line 2) is specific to the lactate dehydrogenase of the P. vivax species (pvLDH). Conjugatepad is dispensed with monoclonal antibodies conjugated to colloidalgold, which are specific to P. falciparum histidine rich protein-2 (PfHRP-2) and specific to the lactate dehydrogenase of P. vivax. Therefore,the antigen of Plasmodium falciparum and Plasmodiumvivax can be differentially detected. Features Of Malaria Test Kit Malaria is a disease serious parasitic characterized by fever, chills, and anemia and is caused by a parasite that is transmitte. The disease now occurs inmore than 90 countries worldwide, and it is estimated that there areover 500 million clinical cases and 2.7 million malaria-caused deathsper year. This Malaria pf&pv test cassette is very sensitive and only takes about 15 minutes. Test results of this malaria check kit can be read visually without any instruments. Storage And Stability Of Malaria Test Kit 1. This malaria rapid test kit can be stored at temperature 2℃ to 30℃ 2. Keep the temperature at 15-30℃ during the test. 3. Keep away from sunlight, moisture and heat. 4. In the sealed pouch to the date of expiration. 5. Patient samples perform best if tested immediately after collection. Now we offer malaria test kit for sale, if you want to buy malaria test kit, please contact us. More information about ivd market, please visit our website. The price of ivd medical device is affordable, any need, please leave us a message.

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Recombinant Human Protein ST2, also known as IL-1 R4 and T1, is an Interleukin-1 receptor family glycoprotein that contributes to Th2 immune responses (1, 2). Soluble ST2(sST2) is a member of the interleukin 1(IL-1) receptor family existing in blood. And it has been already confirmed to have capacity of capturing IL-33, inhibiting IL-33/ST2 signal transferring, and rise significantly in mechanical overloading cardiac cells. As a result, soluble ST2 can be detected in the blood when heart failure or chronic heart failure exacerbation, or heart muscle can not expand and contract because of cicatrization caused by AMI. Specification Of Human Recombinant ST2 Protein Source: E.coli Purification: Affinity purified. Concentration: 1.4mg/ml Buffer: 10mMpbs, PH=7.4, 1mm EDTA,0.1% SKL,0.2%NaN3 Preservative: 0.2%NaN3 Storage & Shelf life: Store at -20C for 3 years. Avoid multiple freeze/thaw cycles. Application Of Human Recombinant ST2 Protein Suitable for use as a standard in immunoassay, immunogen for antisera production, and tracer for iodination. Each laboratory should determine an optimum working titer for use in its particular application. More information about in vitro diagnostic market, please visit our website. If you need in vitro diagnostics, please contact us.

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H.pylori infects more than half the people in the world. The prevalence of the infection varies among countries and among different groups within the same country. The prevalence rate in the United State suggests an incidence of infection of 2%. The lifetime prevalence of peptic ulcer disease is about 12% in men and 9% in women. Studies have found that more than 90% of patients with duodenal ulcer and 80% of patients with gastric ulcer are infected with helicobacter pylori breath test kit detects the presence of H.pylori antigens in stool specimens. Expected values for any given population should be determined for each laboratory. The positivity rate of any given laboratory may vary depending on geographic location, ethnic group, and living environment. Features Of H.pylori Test Kit This h pylori test kit is for qualitative detection of H. pylori antigen in stool sample and dose not indicate the quantity of the antigens. This h pylori test kit is for in vitro diagnostic use only. This h pylori test kit result should be used only to evaluate with patient with signs and symptoms of gastrointestinal disease. A definitive clinical diagnosis should only be made by the physician after all clinical and laboratory finding have been evaluated. Principle Of H.pylori Test Kit H. pylori Antigen Rapid Test Kit simplified as h pylori kit, is a sandwich solid phase immunochromatographic assay. To perform the test, an aliquot of diluted stool sample is added to the sample well of the test cassette. The sample flows through a label pad containing H. pylori antibody coupled to redcolored colloidal gold. If the sample contains H. pylori antigens, the antigen will bind to the antibody coated on the colloidal gold particles to form antigen-antibody-gold complexes. These complexes move on the nitrocellulose membrane by capillary action toward the test line region on which H. pylori specific antibodies are immobilized. If you want to buy h pylori test kit, please contact us. More information about in vitro diagnostics market, please visit our website. As one of in vitro diagnostics companies, we also have various types of ivd products for sale, anything you need, leave us a message.

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Hepatitis C Virus (HCV) is a small, enveloped, positive-sense, single- stranded RNA Virus. HCV is now known to be the major cause of parenterally transmitted non-A, non-B hepatitis. Antibody to HCV is found in over 80% of patients with well-documented non-A, non-B hepatitis. Conventional methods fail to isolate the virus in cell culture or visualize it by electron microscope. Cloning the viral genome has made it possible to develop serologic assays that use recombinant antigens. Features Of HCV Test Kit Compared to the first generation HCV EIAs using single recombinant antigen, multiple antigens using recombinant protein and/or synthetic peptides have been added in new serologic tests to avoid nonspecific cross-reactivity and to increase the sensitivity of the HCV antibody tests. Rapid hcv test kits (Whole Blood/Serum/Plasma), also known as hepatitis c test kit or hep c test kit, is a rapid test to qualitatively detect the presence of antibody to HCV in a whole blood, serum or plasma specimen. The test utilizes colloid gold conjugate and recombinant HCV proteins to selectively detect antibody to HCV in whole blood, serum or plasma.There combinant HCV proteins used in the test kit are encoded by the genes for both structural (nucleocapsid) and non- structural proteins.The HCV Rapid Test Kit (Serum / Plasma/ Whole Blood) is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in whole blood, serum or plasma. Convenient and quick to perform at-home hepatitis c test. Material Of HCV Test Kit Materials Provided: 1. 25 Individual sealed pouches, each containing: Test device Desiccant pouch Extraction tubes 2. One extraction buffer in a dropper bottle (6mL): 0.01M phosphate buffer saline (PBS). Material Required But Not Provided: Timer If you want to know more about hcv rapid test price and hcv rapid test kit procedure, please contact us. As one of hcv test kit manufacturers, we will provide more high quality ivd test kits for customers, anything you need, leave us a message. More information about ivd diagnostics, please contact us.

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Rapid test for ebola (Colloidal gold method) is intended for the qualitative detection of ebola antigens from Nose swabs. This rapid test for ebola is intended to be used as an aid in the diagnosis of ebola, secretion of patients, and the incubation period of infection is 2-21 days. All the infected patients had high fever, headache, sore throat, weakness and muscle pain. Then there's vomiting, abdominal pain, diarrhea. Within two weeks after the onset of the disease, the virus overflowed, leading to internal and external bleeding, blood coagulation, necrotic blood quickly spread to all organs of the body, patients eventually appear oral, nasal and anal bleeding and other symptoms, patients can die within 24 hours. In about 1500 confirmed Ebola cases, the mortality rate is as high as 88% We have ebola test kit for sale, if you have needs, contact us. As one of in vitro diagnostics companies, we also have various types of ivd raw materials for sale, anything you need, leave us a message.

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Dengue virus is an enveloped, single-stranded, positive-sense RNA virus that comprises four related but distinct serotypes (Den 1, 2, 3, and 4). The virus is transmitted by mosquitoes of the daytime-biting Stegomyia family, principally Aedes aegypti and Aedes albopictus. Today, more than 2.5 billion people living in the areas of tropical Asia, Africa, Australia and the Americas are at risk for dengue infection. An estimated 100 million cases of dengue fever and 250,000 cases of life- threatening dengue hemorrhagic fever occur annually on a worldwide basis. Serological detection is a common method for the diagnosis of infection with dengue virus. IgM anti-dengue virus starts to appear at 3 days after initial exposure and remains in circulation for about 30- 60 days. IgG anti-dengue virus is raised at around 7 days, peaks at 2-3 weeks and persists for the duration of life4-6. Detection of antigens released during virus replication in the infected patient show very promising results; it enables diagnosis from the first day after the onset of fever up to day 9 once the clinical phase of the disease is over, thus, allowing early detection and prompt treatment. Features of dengue duo rapid test kit The Dengue Ag NS1-IgM/IgG rapid test detects IgG and IgM anti-dengue virus and circulating dengue antigen in one test within 20 minutes. This dengue rapid test kit is user-friendly, does not require cumbersome laboratory equipment and requires minimal staff training. The Dengue NS1+IgM/IgG Combo rapid test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG anti– dengue virus, IgM anti-dengue virus and dengue antigen (Dengue Ag) in human serum, plasma or whole blood. It is intended to be used by professionals as a screening test and as an aid in the diagnosis of infection with dengue virus. Any reactive specimen with the Dengue Ag NS1-IgM/IgG rapid test must be confirmed with alternative testing method(s). Precautions Of Dengue Test Kit 1. For in vitro diagnostic use and professional use only. 2. Read the package insert instruction before use the kit. 3. Do not use beyond the expiration date which appears on the package label. 4. Do not open the sealed pouch, unless ready to conduct the assay 5. Bring all reagents to room temperature (15°C-30°C) before use. 6. Haemolized blood may be used for the testing, but do not take precipitants. 7. Wear protective clothing and disposable gloves while assaying samples. Wash hands thoroughly after performing the test. 8. Handle all specimens as if they contain infectious agents. When the assay procedure is completed, dispose of specimens carefully after autoclaving them for at least one hour. Alternatively, they can be treated with 0.5 to 1% solution of sodium hypochlorite for one hour before disposal. 9. Do not smoke, drink, or eat in areas where specimens or kit reagents are being handled. 10. Read result after 30 minutes may give erroneous results. 11. Do not perform the test in a room with strong air flow, an electric fan or strong air-conditioning. 12. As with all diagnostic tests, a definitive clinical diagnosis should not be based on the results of a single test, but should only be made by the physician after all clinical and laboratory findings have been evaluated. 13. Excess sample volume (>5µL) can give false positives Now the dengue ns1 price is affordable, if you want to buy dengue test kit, please contact us. If you need ivd in vitro diagnostic, please leave us a message. More types of in vitro diagnostic products, please visit our website.

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