CTK biotech, OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood. CE certified.
Product Details: Number of Reactions(Preps)/Kit : 30T Brand : CTK Biotech Result Time (Rapid Kits) ; 20mins Sample Type : Blood Test Type : Rapid Test CAT No : R0066C The OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood.
1. PROTAN COVID-19 IgM/IgG Protan Covid-19 IgM/ IgG is In-Vitro kit for the qualitative measurement of anti-COVID-19 IgM and IgG antibodies in human whole blood, plasma, and serum which non-medical professionals can use. It produces results in 15 minutes without additional analyzer and is for easy, simple and rapid test just with finger tip blood. 2. PROTAN COVID-19 IgG Type2 In-Vitro kit for the qualitative measurement of SARS-Cov-2 IgG antibodies against SP-RBD in human whole blood, plasma, and serum. Protan Covid-19 IgG Type2 neutralizing Antibody Rapid Test Kit is to check whether the formation of Covid-19 Neutralizing antibodies After vaccination. Protan Covid-19 IgG Type2 is intended for the detection of neutralizing antibodies(IgG) against Covid-19 SP RBD(spike protein-receptor binding domain) in Human whole blood after vaccination.
VETLabs Toxoplasma IgM/IgG test is a sandwich lateral flow immunochromatographic assay, developed and manufactured by Bioguard Corporation, for the rapid and qualitative detection of Toxoplasma IgM/IgG in cat's blood. The test device has a testing window, coated by an invisible T (test) zone and C (control) zone. When a sample is applied to the sample well on the device, the reagent will laterally flow on the surface of the test strip. If there is enough Toxoplasma IgM/IgG in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid test. By the means, the device can accurately indicate the presence of Toxoplasma IgM/IgG in the specimen. Kit components: 5 test per box and/or 10 test kit per box in an individual foil pouch with a desiccant and disposable dropper, EDTA blood collection tube, Assay buffer bottle, Instruction manual
We have igg /igm co-19 rapid test made in canada with CE ready in stoke dubai -uae
CTK Biotech's, CE Certified , the OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Product Description Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity Differentiates Between Igg And Igm To Determine Stage Of Infection One Step Procedure Minimizes Operator Error Due To Sample Preparation High Level Of Reproducibility Test Kits Can Be Used And Stored In A Wide Range Of Temperatures Product Specification:- Brand Name : CTK Biotech Pkg Qty : 1 Number Of Items : 30 Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
This product is the rapid testing of COVID-19, the result come out within 10 minutes.
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
INTENDED USE For qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in serum, plasma (EDTA, sodium citrate and lithium heparin) or fingerstick whole blood, venous whole blood specimens from patients suspected of COVID-19 infection. FEATURES Coated with carefully selected specific Nucleocapsid and Spike protein antigen. Detection for IgM and IgG antibodies simultaneously. Simple operation, easy result interpreted. Rapid test within 15 minutes. RESULTS INTERPRETATION Positive: 1. The presence of 3 red lines (T1, T2 and C) within the reaction window, no matter which band appears first, indicates presence of both SARS-CoV-2 IgM and IgG antibodies. 2. The presence of 2 red lines (T1 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgM antibody. 3. The presence of 2 red lines (T2 and C) within the reaction window, no matter which band appears first, indicates presence of SARS-CoV-2 IgG antibody. Negative: 1. The presence of line (control line) only within the reaction window indicates that no SARS-CoV-2 antibodies are detected. The results is negative. Invalid: 1. If the control(C) line is not displayed in 10-15 min, regardless of whether T1 and/or T2 line is present, the test result is invalid. It is recommended that the specimen should be re-tested. 2. The test result is invalid after 15 min. CLINICAL PERFORMANCE - Positive Percent Agreement (PPA) = 91.07% (153/168) (95% CI: 85.70%-94.92%). - Negative Percent Agreement (NPA) = 95.37% (103/108) (95% CI: 89.53%-98.48%). - Overall Rates of Agreement (ORA) = 92.75% [(153+103)/ (168+108)] (95% CI: 89.03%-95.52%). [Product Name]: SARS-CoV-2 IgM/IgG Duo Test [Product Code]: Cat# FP-319 [Sample Type]: Whole blood /Plasma/Serum [Sample Volume]: 20L /10L/10L [Detection Method]: Colloidal Gold [Reaction Time]: 10-15min [Packing Size]: 1T x 20 cassettes per box + Sample diluent 1 vial x 5mL. [Storage Condition]: 2oC ~ 30oC [Shelf Life]: 12 months [CE Mark Registration No.]: RPS/499/2021.
COVID-19 IgM/IgG test kit (Colloidal Gold) This kit is used for the qualitative determination of COVID-19 IgM/IgG antibodies in human serum, plasma and venous whole blood samples in vitro. as an auxiliary diagnosis of COVID-19 infection. [Detection principle] This kit uses colloidal gold immunochromatography. Testing COVID-19 IgG antibody and COVID-19 IgM antibody in human serum, plasma and whole blood samples. The blood samples diluent containing COVID-19 IgG antibody and/or COVID-19 IgM antibody chromatography to colloidal gold binding pad, recombinant with colloidal gold marked COVID-19 antigen antibody, forming colloidal gold - antigen complex, chromatography to test area, combining to precoated anti-human IgG antibody and/or anti-human IgM antibody respectively, forming complexes in the test area and presenting red precipitation line. Unbound rabbit IgG colloidal gold bond chromatography to quality control line (C) combined with precoated sheep anti-rabbit IgG antibody presented a red precipitation line. If the samples do not contain COVID-19 IgG antibody and/or COVID-19 IgM antibody, there is no corresponding red precipitation line existed in the test area. A red precipitation line appears on the quality control line (C) no matter if there is COVID-19 IgG antibody and/or COVID-19 IgM antibody in the sample or not. [Storage and Stablity] 1. Store at 2ï½?30 for 18 months in a cool place, no direct sunlight and no freeze preservation. The test card and sample diluent should be used up in 1 hour after opening the package (opening temperature 10~30, humidity 25%~95%). 2. The date of production and the term of use are labeled.
Our Covid-19 rapid test kits are a serology test using a novel way to identify to identify exposure to the Covid-19 virus by the identification of the IgM/IgG antibodies through a sample of serum, plasma or whole blood. The presence of the antibodies is revealed in 15 minutes and does not require any specialised laboratory equipment for the execution of the test. Test kits are packaged with 25 sealed pouches holding the test cassettes, an instruction set, 25 capillary tubes for making 25 tests and a bottle of 3ml with buffer solution to execute 25 tests. The test pouch contains the test cassette and a sterilizer pad to be used to disinfect the fingertip in case of fingerprint blood sampling. (A) Name of product: COVID-19 IgM/IgG Antibody Rapid Test (B) Price $4 EXW (c) Origin: Canada (d) Features: Artron COVID-19 IgM/IgG Antibody Test is a rapid, qualitative, and convenient immunochromatographic in vitro assay for the differential detection of IgM &/or IgG antibodies to SARS-COV-2 in human serum, plasma or whole blood samples. The device is designed to aid in the determination of recent or previous exposure to SARS-COV-2 virus tracking the bodyâ??s immunity status to the virus after SARS-COV-2 infection. (E) HS code:382200 (F) 20,000 units (g) Carton Size (LxWxH cm) 59*41*37 - 2,200 test per carton. 17.6kg. 25,000 kits per pallet.
Our COVID-19 rapid test kit can be used effectively on many levels for proper screening and strategic preparedness toward the pandemic. The test kit requires no sophisticated equipment nor laboratory settings. Our SARS-COV-2 Antibody Rapid Test Kit can be applied for screening of COVID-19 disease on the following: General practitioners and external clinics level to detect previous SARS-COV-2 viral infections on both symptomatic and asymptomatic patients. Determination of the immunity level of front-line healthcare workers, which can help in the development of pandemic preparedness strategies at national levels. Epidemiological COVID-19 surveys at national and district levels for research purposes. Airport screening for arriving /departing passengers to control the pandemic in the aviation industry. Suspected cases exclusion to minimize cost and time spent in the RT-PCR testing procedures. Screening on the national level to facilitate decision making regarding lockdown and curfew easing strategies. Phoenix Bioscience is offering a competitive price for a high-quality kit that is made in Canada and used currently to combat the pandemic in most American cities.
Covid Ab IgG/IgM Ab Whole blood test device Sensitivity: 86.94% Specificity: 99.31% Accuracy: 93.36%
The Diagnostic Kit for SARS-CoV-2 IgM/IgG Antibody (Colloidal Gold) adopts the solid phase colloidal gold immunochromatographic technology for the qualitative determination of IgM/IgG antibodies against SARS-CoV-2
The Diagnostic Kit for SARS-CoV-2 IgM/IgG Antibody (Colloidal Gold) adopts the solid phase colloidal gold immunochromatographic technology for the qualitative determination of IgM/IgG antibodies against SARS-CoV-2
COVID19 IgG & IgM Antibody Detection Kit FROM TAIWAN,ALL MADE IN TAIWAN
Name Testing kit for New coronavirus (2019-nCOV) IgG/IgM antibody Rapid Test WB/S/P Specifications 25 tests Introduce This kit uses the colloidal gold immunochromatographic principle to qualitatively detect novel coronavirus igg/igm antibodies in human serum, plasma, or whole blood. the sample to be tested was added to the sample hole of the test paper, and then added 2 drops of sample diluent. the igg/igm antibody in the sample combined with the recombinant new coronavirus antigen labeled with the colloidal gold on the binding pad formed complex. under the action of chromatography, it diffused forward along the nitrocellulose membrane (nc membrane). the nitrocellulose membrane was fixed with two detection lines (g line, m line) and one quality control line (c line). the g line was fixed with anti-human igg antibody for the detection of new coronavirus igg antibody; the m line was fixed with anti-human igm antibody for the detection of new coronavirus igm antibody; and the c line had quality control for the detection of the new coronavirus ig antibody. If the sample contains a new coronavirus IgG antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human IgG antibody fixed on the NC membrane detection line (G line). if the sample contains a novel coronavirus igm antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human igm antibody fixed on the nc membrane detection line (m line). The darker the color of the colloidal gold accumulated on the detection line, the higher the concentration of the new coronavirus antibody in the sample. To monitor the effectiveness of the test card, set up a quality control line (line C), whether there is a detection line (line T), quality control line (line C) should be color, otherwise the test results are judged invalid. Storage Stored at 4 to 30c and valid for 18 months. After the aluminum foil bag is unsealed, please use it as soon as possible. Sample 1. It is suitable for human serum, plasma and whole blood samples. 2. The samples should be used as soon as possible; if they cannot be used immediately, the serum / plasma samples should be kept at 2-8C for 5 days and -20C for long-term preservation; the whole blood samples should be placed at 2-8C to avoid hemolysis; 3.The sample contains a large amount of lipids, hemolysis or turbidity, do not use, so as not to affect the judgment of the results.
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
USA: FDA EUA APPROVED Approved for Import to European Union Approved by Chinese Government (CFDA) for Export Qualitative detection of the presence of IgM & IgG antibody to COVID-19 in Human serum, plasma and whole blood Results available in 10 minutes Component: Cassette, Sample Diluent, Pipette and Test Card
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.
