COVID19 IgG & IgM Antibody Detection Kit FROM TAIWAN,ALL MADE IN TAIWAN
To evaluate the sensitivity of Artronâ??s COVID-19 IgM/IgG antibody (Ab) rapid diagnostic device (RDT). Accuracy up to 97.7% 30 min test
Coronavirus IgG/IgM Dual Detection Kit: *****Just approved for marketing by Taiwan Food and Drug Administration, Ministry of Health and Welfare , It is the fastest (around 2-3 minutes) and the most accurate up to 97.3% comparing with global test kit. Made in Taiwan It can save the life because some hospitals require a confirmed test report ,then just will allow you to be hospitalized. Patients can get the fastest treatment and master the golden treatment time!!!
COVID-19 IgM/IgG Antibody Detection Kit (Colloidal Gold Immunochromatography) is suitable for the qualitative detection of COVID-19 by detecting SARS-CoV-2 IgM/IgG antibodies in human serum, plasma, or whole blood. Common signs of infection with SARS-CoV-2 include respiratory symptoms, fever, cough, shortness of breath, and dyspnea. In more severe cases, infection can cause pneumonia, severe acute respiratory syndrome, kidney failure, and even death. SARS-CoV-2 can be excreted through respiratory secretions or transmitted through oral fluids, sneezing, physical contact, and through air droplets
The Typhoid IgG/IgM Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of anti-Salmonella typhi (S. typhi)G and IgM in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with S. typhi. Any reactive specimen with the Typhoid IgG/IgM 2.0 Rapid Test must be confirmed with alternative testing method(s).
The Cytomegalovirus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of Cytomegalovirus (CMV) in human serum/plasma samples. Cytomegalovirus is a herpes virus and a leading biological factor causing congenital abnormalities and complications among those who receive massive blood transfusions and immunosuppressive therapy. About half of the number of pregnant women who contract a primary infection, spread the disease to their fetus. When acquired in-utero, the infection may cause mental retardation, blindness, and/or deafness. Serological tests for detecting the presence of antibody to CMV can provide valuable information regarding the history of previous infection, diagnosis or active or recent infection, as well as in screening blood for transfusions in newborns and immuno-compromised recipients. The Cytomegalovirus Rapid Test Device (Serum/Plasma) has been designed to detect CMV through visual interpretation of color development in the internal strip. The membrane was immobilized with antigens of CMV on the test region. During the test, the specimen is allowed to react with colored recombinant mouse anti-human IgM latex conjugates, which were precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents on the membrane. If there were enough CMV antibodies in specimens, a colored band will from at the test region of the membrane. Presence of this colored band indicates a positive result, while its absence indicates a negative result. Appearance of a colored band at the control region serves as a procedural control. This indicates that proper volume of specimen has been added and membrane wicking has occurred.
INTENDED USE THE ONE STEP ANTI-DENGUE (IGM & IGG) TRI-LINE TEST IS A COLLOIDAL GOLD ENHANCED, RAPID IMMUNOCHROMATOGRAPHIC ASSAY FOR THE QUALITATIVE DETECTION OF ANTIBODIES (IGM & IGG) TO DENGUE VIRUS (DV) IN HUMAN WHOLE BLOOD, SERUM OR PLASMA. THIS TEST IS A SCREENING TEST, AND ALL POSITIVES MUST BE CONFIRMED USING AN ALTERNATE TEST SUCH AS WESTERN BLOT. THE TEST IS INTENDED FOR HEALTHCARE PROFESSIONAL USE ONLY. 25PCS/BOX
Novel Coronavirus (2019-nCoV) Real-time RT-PCR Kit is a real-time RT-PCR test intended for the qualitative detection of nucleic acid from the 2019-nCoV in oropharyngeal swabs and bronchoalveolar lavage fluid collected from individuals suspected of COVID-19 by their healthcare provider. A kit contains: Package specifications: 24 tests/kit, 48 tests/kit 1) 2019-nCoV-PCR Master Mix (Lyophilized Powder): 1 bottle/box 2) 2019-nCoV-PCR Positive Control (Lyophilized Powder):1 bottle/box 3) 2019-nCoV Diluent: 1 bottle/box 4) User Manual
A serology test or Antibody Rapid Test which doesn't test for the virus itself. Instead, it look for body's immune response to the virus. This test is getting popular is not only because its convenience but also because it can identify whether youâ??ve ever been exposed to SARS-CoV-2 - which would deepen our understanding of who is getting sick, particularly people who showed few or no symptoms. It could also allow people whose bodies seem to have some degree of immunity to the illness to return to work more quickly. Please email us and get detailed factsheet, certification etc.
COVID-19 IgG/IgM Rapid Test Kit (Colloidal Gold) The accuracy of the rapid test is 93% for IgM detection and 98% for IgG detection, compared to the RT-PCR Tests done at individual labs in The Netherlands. Pricing clears and depends on volumes naturally. Please ask the exact quote with the volume requested information. CE and FDA EUA approved Made in USA, Germany, Canada
Warranty:2 years, 2 Years After-sale Service:Online Technical Support Material:Plastic Shelf Life:2 years Quality Certification:CE Instrument classification:Class II Safety standard:MFDS Product name:antibody test Sensitivity: >85% Specificity: >90% Total coincidence rate: >90% Work environmental temperature: 40 Inspection method:antibody detection Sample dosage:10ul Inspection time: 15min Type of sample:capillary vessel or vein
Specification Strength/ Size Packing Size Packed In Filariasis Kit Includes One test Strip, Desiccant and Dropper 50 Strip Test Per Pack 50 Box Pack
Feline Coronavirus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Coronavirus antibody (FCoV Ab) in cat's blood. Assay Time: 5-10 mins Sample: serum, plasma or blood Feline Coronavirus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FCoV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of Feline Coronavirus antibody in the sample.
General Information One-Step Chikungunya IgG/IgM Rapid Test is detection of IgG and IgM anti-chikungunya virus CHIK in human blood. Sensitivity: 90.3% , Specificity: 100% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
General Information One-Step Leishmania IgG/IgM Rapid Test is detection antibodies IgG and IgM to the subspecies of the Leishmania donovani (L. donovani), the Visceral leishmaniasis causative protozoans in human blood. Sensitivity: 91.2 % , Specificity: 99.5% Specimen : Serum, Plasma or Whole Blood Reading Time : 10 min
Uncut Sheet Strep A IgG/IgM Rapid Test Format:Cassette/Strip Uncut Sheet A rapid test for the qualitative detection of Strep A antigen in throat swab specimens.For professional in vitro diagnostic use only. INTENDED USE The Strep A Rapid Test Strip (Throat Swab) is a rapid chromatographic immunoassay for the qualitative detection of Strep A antigen from throat swab specimens to aid in the diagnosis of Group A Streptococcal infection. SUMMARY Streptococcus pyogenes is non-motile gram-positive cocci, which contains the Lancefield group A antigen that can cause serious infections such as pharyngitis, respiratory infection, impetigo, endocarditis, meningitis, puerperal sepsis, and arthritis.1 Left untreated, these infections can lead to serious complications, including rheumatic fever and peritonsillar abscess.2 Traditional identification procedures for Group A Streptococci infection involve the isolation and identification of viable organisms using techniques that require 24 to 48 hours or longer.3,4 The Strep A Rapid Test Strip (Throat Swab) is a rapid test to qualitatively detect the presence of Strep A antigen in throat swab specimens, providing results within 5 minutes. The test utilizes antibodies specific for whole cell Lancefield Group A Streptococcus to selectively detect Strep A antigen in a throat swab specimen. PRINCIPLE The Strep A Rapid Test Strip (Throat Swab) is a qualitative, lateral flow immunoassay for the detection of Strep A carbohydrate antigen in a throat swab. In this test, antibody specific to Strep A carbohydrate antigen is coated on the test line region of the test. After the test strip is immersed into a specimen, the extracted throat swab specimen reacts with an antibody to Strep A that is coated onto particles. This mixture migrates up the membrane to react with the antibody to Strep A on the membrane and generate a colored line in the test line region. The presence of this colored line in the test line region indicates a positive result, while its absence indicates a negative result. To serve as a procedural control, a colored line will always appear at the control line region, indicating that proper volume of specimen has been added and membrane wicking has occurred.
Antigens, antibodies, uncut sheets, and finished ivd test kits.
High accuracy High quality, with CE certificate. 10 tests per box
Novel Coronavirus - Saliva Test Individually Use All Certificates
I. The new coronavirus (2019-nCoV) antibody detection kit is used to quickly and qualitatively detect the new coronavirus IgM / IgG antibodies in human whole blood, serum, and plasma. The fastest test results can be obtained by naked eye within 15 minutes. 2. What are the advantages of the new coronavirus detection kit? -Combined detection with nucleic acid improves detection rate. -Sampling problems can cause false negatives in nucleic acid testing, and antibody testing can be avoided. -Antibodies testing can help improve the diagnosis of suspected cases. -Low laboratory requirements, which are conducive to the wide deployment of hospitals at all levels. -Epidemiological research provides supporting data. 3.the characteristics of colloidal gold detection method: -Fast detection: results are available within 10 minutes. -Easy to observe: judge with the naked eye. -Suitable for large-scale rapid screening 4. scope of application It can be applied to outpatient and emergency room and ward testing, especially to community health service centers, primary hospitals, tertiary hospitals, outpatient emergency clinics, early screening of hot outpatient clinics, and physical examination screening for incumbent employees of various enterprises and institutions. 5.Operation steps Keep the experimental environment: temperature 15 ~ 30 , humidity 30% ~ 70%. -Remove the kit and equilibrate at room temperature for 20-30 minutes. -Add 2 drops of washing solution to the reaction well, and wait for the liquid to completely wet the membrane. -Add 50 μL of the test serum to the reaction well, and allow the liquid to be fully inhaled. -Add 2 drops of washing solution to the reaction well, and wait for the liquid to be fully aspirated. -Add 3 drops of gold standard solution to the reaction well, and allow the liquid to be fully aspirated. -Add 3 drops of washing solution to the reaction well, and observe the result within 3 minutes after the liquid is fully inhaled. 6.matters needing attention -Do not ingest food or smoke when collecting specimens. Wear disposable gloves and wash your hands afterwards. -The antibody detection kit is very sensitive to humidity. Pay attention to the decrease in function caused by humidity. -When removing the reagent, avoid touching the test line with your hand or other foreign objects. -When judging the results, pay attention to repeated freezing or dissolution may bring false negative or false positive results.
