Covid-19 Rapid Test kit(IgG/IgM) - Made in USA (Its made in USA product with Korean technology) - Product will be dispatched from USA. - Package : 25 Tests/Kit - Price : FOB USA(New Jersey), USD 13/test - MOQ : 100,000 test - Lead time : immediately (In stock) - USA FDA EUA approved - CE approved
Covid-19 Rapid Test Kits OTG USA-Price based upon order. Worldwide shipping.
Antigen-COVID-19 Virus Test Kit (Colloidal gold) 25pcs/kit High quality Fast delivery CE certified
COVID-19 real-time RT-PCR Kit is designed for the qualitative detection of COVID-19 viral RNA in oropharyngeal swab, nasopharyngeal swab, sputum and bronchoalveolar lavage (BAL).kit includes primers and probe set targeting the human RNase P gene that serves as an internal positive control for the real-time RT-PCR. price depends on MQO, Payment LC or TT
Product Description : Solid phase immunochromatographic test kit for the rapid and differentiated detection of IgG and IgM antibodies in blood, plasma or blood serum. Price of product ( USD price or FOB price) : USD 14,68 Product origin : China Key Specifications/Special Features : Test Kit: Blood / serum / plasma Minimum Order Size and Packaging details : Packing 1, 5, 10 , 25 units, Minimum Order Quantity
Rapid diagnostic test kits
Rapid pregnancy test cassette form
This product is used for in vitro qualitative detection of SARS-CoV-2 antigen in human oropharyngeal swabs, nasal swabs and nasopharyngeal swabs. It is helpful as an aid in the screening of early mild, asymptomatic, or acute patients for identification of SARS-CoV-2 infection.
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Rapid SAR-CoV-2 (Covid-19) Test Kits: FDA & CE Approved (Results in 15 min). SAR-CoV-2 IgG/IgM Rapid Test Cassette is a qualitative membrane based immunoassay for the detection of IgG and IgM antibodies to SAR-CoV-2 in human whole blood, serum or plasma specimen. Made in China: FDA and CE Approved, China NMPA approval (export allowed) One of the earliest CE (Feb 2020) and FDA (Mar 2020) approved kit. Clinically studied and reliable. Packaging: 20 sets/box or 40 sets/box. Payment term: MOQ 2000 sets, FOB China $ 9.5/set. < 10000 sets 100% advance payment > 10000 sets L/C ex-work on site
COVID-19 IgG/IgM Rapid Antibody Test Kit with EUA FDA approval. Available immediately! (Whole Blood/Serum/Plasma) is a solid phase immuno chromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to 2019 Novel Coronavirus in human whole blood, serum or plasma. - Fast results as soon as 2-10 minutes - Facilitates patient treatment decisions quickly - Simple, time-saving procedure - Little specimens, only 5L of serum/plasma or 10L of whole blood specimens - All necessary reagents provided & no equipment needed - High sensitivity and specificity - Sensitivity: IgG 97.2%; IgM 87.9% - Specificity: IgG 100%; IgM 100% - Specimen: Whole Blood, Serum, Plasma - Shelf Life: 24 months from the date of manufacture
The FactView Typhoid IgG/IgM Rapid Test Kit is a diagnostic assay used for the qualitative detection of IgG and IgM antibodies specific to Salmonella typhi, the bacterium that causes typhoid fever. Here's more information about this type of diagnostic test: Purpose: The test is used for the rapid diagnosis of typhoid fever, a bacterial infection caused by Salmonella typhi. Typhoid fever is characterized by fever, abdominal pain, headache, and other symptoms, and it can lead to serious complications if not treated promptly. Principle: The FactView Typhoid IgG/IgM Rapid Test Kit is an immunochromatographic assay that detects the presence of IgG and IgM antibodies in a patient's blood sample. IgM antibodies are typically produced during the acute phase of infection, while IgG antibodies are produced later during the convalescent phase. Components: The test kit usually includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific antigens for capturing IgG and IgM antibodies against Salmonella typhi. Procedure: The test procedure involves collecting a small amount of blood from the patient (usually obtained via finger prick) and applying it to the sample well of the test cassette. Buffer solution is then added, allowing the blood sample to migrate along the test strip. Results are typically visible within 15-20 minutes. Interpretation: The appearance of colored lines on the test strip indicates the presence or absence of IgG and IgM antibodies against Salmonella typhi. A visible line in the control region indicates that the test is valid. Additional lines in the test region(s) indicate positive results for IgG and/or IgM antibodies. Sensitivity and Specificity: The FactView Typhoid IgG/IgM Rapid Test Kit demonstrates sensitivity and specificity for detecting typhoid fever. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings. Utility: The rapid detection of IgG and IgM antibodies against Salmonella typhi provides valuable information for diagnosing acute or recent typhoid fever infections, determining immune status, and guiding patient management decisions. Limitations: While rapid diagnostic tests are useful for typhoid fever diagnosis, they have limitations compared to more sensitive methods such as blood culture or molecular testing. Factors such as test sensitivity, specificity, and the timing of specimen collection can influence test performance. Overall, the FactView Typhoid IgG/IgM Rapid Test Kit is an important tool for diagnosing typhoid fever, allowing for timely patient management and implementation of control measures. However, results should be interpreted carefully in conjunction with clinical evaluation and other laboratory tests.
Troponin I (CTnI) One Step Rapid Test Kit (Whole blood/serum/plasma) Product description Product name: CTnI One Step Troponin I Rapid Test Kit Specification: Lateral-flow Immunofluorescence Chromatographic Assay 10 pcs, 25 pcs, 50 pcs, 100 pcs/box, or customized Type: Cassette MOQ: 10,000 PCS Analytical Range: 1.0~50ng/ml (Whole Blood); 0.1~50ng/ml (Serum/Plasma) Specimen: Human serum/plasma/whole blood Manufacturer: Hangzhou Laihe Biotech Co., Ltd. 2.Clinical significance (1)Diagnosis of various chest pain (2)Foundation of ACS diagnosis and risk stratification (3)Best markers for ACS prognosis (4)An aid in the diagnosis of myocardial infarction (injury) (5)Can improve clinical, economic and operational outcomes
Catalog Number: FRT02 Type: FAMEX SARS-CoV-2 Saliva Antigen Rapid Test Kit Technical: Rapid Antigen Test Kit Specimen Types: Sputum Claim: Sensitivity .4 Specifity ,3 Contents: Pipette, Test Cassette, Specimen Tube, Medical Waste Bag, Silica Gel Storage: 2 C -30 C Shipment Type: 2 C -3 C Analysis Time: 15 Minutes Shortly : This kit is used for the qualitative detection of SARS-CoV-2 antigen in vitro environment. It is a lateral flow sandwich assay designed for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 directly in saliva.Packaging, package leaflet and manual customized for various markets.
Catalog Number: FRTFT02 Type: FAMEX SARS-CoV-2 NASOPHARYNGEAL AG RAPID TEST KIT Technical: Rapid Antigen Test Kit Specimen Types: Nasopharyngeal Swab Claim: Sensitivity .7- Specifity .06 Contents: Swab, Test Cassette, Specimen Tube, Medical Waste Bag,Silica Gel Storage: 2C - 30 C Shipment Type: 2 C- 30 C Analysis Time: 15 Minutes Shortly: This kit is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 Nucleocapsid Protein in Nasopharyngeal Swab as an aid in the scientific research of primary and secondary COVID- 19 infections.Packaging, package leaflet and manual customized for various markets.
The current test kit is based on specific antibody antigen reaction and immunoassay technique. The test card contains a gold labeled novel coronavirus N protein monoclonal antibody p re coated on the binding pad and a paired novel coronavirus N protein monoclonal antibodies fixed in the test line (T) and corresponding antibodies in the quality control line (C). During the test, the N protein in the specimen binds to the gold-labeled nove lcoronavirus N protein antibody pre-coated on the binding pad, and the conjugate moves upward under the capillary effect, and then is trapped by N protein monoclonal antibody conjugate fixed in the Test Line (T). The higher the N protein content in the specimen, the more conjugates are trapped, and the darker the color of the Test Line (T). If there is no novel coronavirus in the specimen or the virus content is below the detection limit, no colour appears in the Test Line (T). A purple red band will app ear in the Control Line (C) regardless of whether there is a virus in the specimen. The purple red band that appears in the Control Line (C) is the criteria for determining whether there is enough specimen and whether the chromatography process is normal.
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is an immunofluorescent sandwich assay. It can detect the virus with very high sensitivity and specificity. When the sample is applied to the sample wells, SARS-CoV N protein and labeled antibody complexes are formed and travel up the strip. The labeled microsphere fluorescent probe reagent is used to form a visible red line with a matched UV flashlight. The presence of SARS-CoV-2 will be indicated by a visible red test line (T) in the result window. The membrane is pre-coated with Chicken IgY on the control (C) line. Control (C) line appears in each result window when the sample has flowed through the strip.
Product Details: Brand J.Mithra Test Kit Type HBsAg Test Kit (Rapid) Detects All the 11 subtype of HBsAg Sensitivity 100% by WHO Evaluation Specificity 100% by PATH USA Evaluation Cat. No HB010100 Intended Use : Hepacard is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV). Salient Features: Detects all the 11 subtype of HBsAg. Antigen Sensitivity- 0.5 ng/ml. No sample preparation required. See through Device for easy result interpretation. Shelf life-30 months at 2-30C. WHO Evaluated with 100% Sensitivity. Evaluations: PATH USA: Sensitivity 100% and Specificity 100% . DEPT. OF CLINICAL VIROLOGY, CMC VELLORE: Sensitivity 100% and Specificity 100% Approved By Drug Controller General Of India( DCGI) For use In Blood Banks.
Specification Strength/ Size Packing Size Packed In Rapid Widal Test Kit (O,H) (2+2) x 5ml Per Pack 1 Box Pack
Product Make: Korea, India, China
