Rapid card test

rapid card test

Right Med brings you world class rapid tests. Our products are proven for their efficacy, reliability and are manufactured under stringent quality control and ISO guidelines.

We continuously strive to innovate and provide affordable simple and easy to use immunoassays which can be performed anywhere. Product Price : Get Latest Price.

rapid card test

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Trop T Sensitive Test. Looking for Rapid Test Cards?Malaria antigen detection tests are a group of commercially available rapid diagnostic tests of the rapid antigen test type that allow quick diagnosis of malaria by people who are not otherwise skilled in traditional laboratory techniques for diagnosing malaria or in situations where such equipment is not available.

There are currently over 20 such tests commercially available WHO product testing The first malaria antigen suitable as target for such a test was a soluble glycolytic enzyme Glutamate dehydrogenase. A major drawback in the use of all current dipstick methods is that the result is essentially qualitative. In many endemic areas of tropical Africahowever, the quantitative assessment of parasitaemia is important, as a large percentage of the population will test positive in any qualitative assay.

Malaria is a curable disease if the patients have access to early diagnosis and prompt treatment. Antigen-based rapid diagnostic tests RDTs have an important role at the periphery of health services capability because many rural clinics do not have the ability to diagnose malaria on-site due to a lack of microscopes and trained technicians to evaluate blood films. Furthermore, in regions where the disease is not endemiclaboratory technologists have very limited experience in detecting and identifying malaria parasites.

An ever increasing numbers of travelers from temperate areas each year visit tropical countries and many of them return with a malaria infection. The RDT tests are still regarded as complements to conventional microscopy but with some improvements it may well replace the microscope.

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The tests are simple and the procedure can be performed on the spot in field conditions. These tests use finger-stick or venous bloodthe completed test takes a total of 15—20 minutes, and a laboratory is not needed. An accurate diagnosis is becoming more and more important, in view of the increasing resistance of Plasmodium falciparum and the high price of alternatives to chloroquine. The enzyme pGluDH does not occur in the host red blood cell and was recommended as a marker enzyme for Plasmodium species by Picard-Maureau et al.

Presence of pGluDH is known to represent parasite viability [2] and a rapid diagnostic test using pGluDH as antigen would have the ability to differentiate live from dead organisms.

Glutamate dehydrogenase provides an oxidizable carbon source used for the production of energy as well as a reduced electron carrier, NADH. Glutamate is a principal amino donor to other amino acids in subsequent transamination reactions. The multiple roles of glutamate in nitrogen balance make it a gateway between free ammonia and the amino groups of most amino acids.

Its crystal structure is published.

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It is well known that enzymes with a high molecular weight like GluDH have many isozymeswhich allows strain differentiations given the right monoclonal antibody. The host produces antibodies against the parasitic enzyme indicating a low sequence identity. The histidine-rich protein II HRP II is a histidine - and alanine -rich, water-soluble protein, which is localized in several cell compartments including the parasite cytoplasm. The antigen is expressed only by P. A substantial amount of the HRP II is secreted by the parasite into the host bloodstream and the antigen can be detected in erythrocytesserumplasmacerebrospinal fluid and even urine as a secreted water-soluble protein.

It generally takes around two weeks after successful treatment for HRP2-based tests to turn negative, but may take as long as one month, which compromises their value in the detection of active infection. Nevertheless, the kinetic properties and sensitivities to inhibitors targeted to the cofactor binding site differ significantly and are identifiable by measuring dissociation constants for inhibitors which, differ by up to fold.Rapid diagnostic tests RDTs are diagnostic assays designed for use at the point-of-care POCand can be adapted for use in low-resource settings.

An RDT is low-cost, simple to operate and read, sensitive, specific, stable at high temperatures, and works in a short period of time. RDTs are already in use for several neglected diseases. Rapid diagnostic tests RDTs are a type of point-of-care diagnostic, meaning that these assays are intended to provide diagnostic results conveniently and immediately to the patient while still at the health facility, screening site, or other health care provider.

Receiving diagnosis at the point of care reduces the need for multiple visits to receive diagnostic results, thus improving specificity of diagnosis and the the chances the patient will receive treatment, reducing dependence on presumptive treatment, and reducing the risk that the patient will get sicker before a correct diagnosis is made.

Rapid tests are used in a variety of point-of care-settings—from homes to primary care clinics or emergency rooms -- and many require little to no laboratory equipment or medical training. RDTs can be especially useful with patient samples that can be collected by minimally trained health personal, such as community health workers. However, capillary blood collection techniques, such as those used for malaria RDTs, demonstrate that innovation in sample collection can be used to improve the utility of RDTs in low resource settings.

Rather than one specific type of technology, rapid diagnostic tests can be built in a variety of platforms, each with their own benefits and limitations. These tests generally involve the interaction of a fixed reagent of either target antigen or antibody that is linked to some type of visible detector, that then reacts with a patient sample. Other types of technologies, such as nucleic-acid amplification, may be too expensive and require too much advanced technology to be applicable as a point of care test.

Rapid diagnostic tests have particular value as epidemiological tools, in addition to use as diagnostics.

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They enable a rapid screening of a potentially affected population, and can be used, as is the case with lymphatic filariasis, as a test of cure to determine when a mass drug administration has been successful.

RDTs are less necessary for diseases that are generally accurately diagnosed syndromically, but could prevent over-prescription of antibiotics if used to differentially diagnose fever or diarrhea, respectively.

There are several different platforms commonly used to build rapid diagnostic tests.

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The relative utility of common RDT platforms is summarized below. Lateral flow tests are the simplest type of RDT, requiring only very minimal familiarity with the test and no equipment to perform, since all of the reactants and detectors are included in the test strip.

In a lateral flow test, the sample is placed into a sample well and migrates across the zone where the antigen or antibody is immobilized. The results are read after a certain amount of time has passed. Another type of RDT, a flow-through test, obtains results even faster than lateral flow tests, but requires an added wash and buffer step, which can limit its portability and stability.

An agglutination test works very simply by observation of the binding of carrier particles and target analytes into visible clumps, seen either through a microscope or with the naked eye.

However, if the binding of the particles is weak, the results of the test can be inconclusive. Dipstick format RDTs with binding sites to test for multiple antigens work by placing the dipstick in a sample. The dipstick is then washed and incubated to prevent non-specific analyte binding.

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These additional steps can limit their usability in low-resource point of care settings. Using electrochemical sensors, these tests would include all detectors and reactants in a single portable cassette.

For more information, see the Diagnostics Innovation Map Report. The limitations and advantages of each of these test types is summarized in the table below. The general weaknesses of RDTs including their subjective interpretation of readout, low throughput, often limited sensitivity relative to laboratory or reference tests, and need for quality control mechanisms. The following table summarizes the strengths and weaknesses of several RDT platforms:.Medical professionals, medical facility employees, individuals paying with Medicaid or private insurance Tax Forms.

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Call Us Medical professionals, medical facility employees, individuals paying with Medicaid or private insurance Cancel Send. Features The ASI RPR rapid plasma reagin Card Test for syphilis is a qualitative and semiquantitative nontreponemal flocculation test for the detection of reagin antibodies in human serum and plasma as a screening test for serological evidence of syphilis All testing materials provided 3 levels of liquid controls included: reactive, weak reactive, nonreactive More ….

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Professionals Also Viewed Product Specifications. Professionals Also Viewed. View Full Comparison. Features The ASI RPR rapid plasma reagin Card Test for syphilis is a qualitative and semiquantitative nontreponemal flocculation test for the detection of reagin antibodies in human serum and plasma as a screening test for serological evidence of syphilis All testing materials provided 3 levels of liquid controls included: reactive, weak reactive, nonreactive Color-coded dropper vials Warp resistant coated test cards Screw cap vials - no glass ampules.Kachi Guda, Hyderabad, Telangana.

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Alcohol Swabs.Kachi Guda, Hyderabad, Telangana. GST No. Product Price : Get Latest Price. The conjugate contains colloidal gold conjugated to Pf specific monoclonal anti- HRP-2 antibody and monoclonal anti-pan specific pLDH antibody. The test sample is added to the device. On addition of assay buffer, the red blood cells get lysed. If the sample contains P. This complex migrates through the nitrocellulose strip by capillary action.

When the complex meets the line of the corresponding immobilized antibody, the complex is trapped forming a purplish pink band which confirms a reactive test result. Absence of a coloured band in the test region indicates a negative test result. To serve as a procedural control an additional line of anti-mouse antibody has been immobilized on the strip as control.

When a sample is added to the device,IgG and IgM antibodies in the sample react with red particles coated with Dengue proteins.

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A red procedural control line should always develop in the test device window to indicate that the test has been performed properly. The systematic identification and treatment of infected individuals will reduce the malaria reservoir in the community and thereby drive down transmission. Test line is coated with anti-dengue NS1 Ag. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloidal conjugate making antigen antibodies complex.

When a sample is added to the device, IgG and IgM antibodies in the sample react with anti-human IgM or IgG antibodies coated on the membrane respectively.

Colloidal gold complexes containing dengue antigens is captured by the bound anti-dengue IgM or IgG on respective test bands located in the test window causing a pale to dark red band to form at the IgG or IgM region of the test device window. By quickly and accurately identifying HIV positive patients earlier, you can increase case finding and facilitate fast and appropriate linkage to care.

This helps close the window period and enables increased case finding at a time when individuals are highly infectious.

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