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
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.
General Information One-Step Dengue Rapid Test is to detect IgG&IgM antibodies in serum, plasma or whole blood. For Dengue IgG/IgM Ab test: Sensitivity : 99.9% , Specificity : 99.5% Specimen : Serum , Plasma and Whole Blood Reading Time : 10 min
Product Details: Number of Reactions(Preps)/Kit : 10T Brand : CTK BioTech Result Time (Rapid Kits) : 10 min Sample Type : Blood Test Type : Rapid test CAT No : R0063C Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 auL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)
A rapid test for the qualitative detection of antibodies (IgG and IgM) to Dengue virus in whole blood, serum, or plasma. For professional in vitro diagnostic use only. INTENDED USE The Dengue IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to Dengue virus in human whole blood, serum, or plasma as an aid in the diagnosis of primary and secondary Dengue infections. DIRECTIONS FOR USE Allow the test device, specimen, buffer, and/or controls to reach room temperature (15 30°C) prior to testing. 1.Bring the pouch to room temperature before opening. Remove the test device from the sealed pouch and use it as soon as possible. 2.Place the test device on a clean and level surface. For Serum or Plasma Specimens: Hold the dropper vertically, draw the specimen up to the Fill Line (approximately 5 μL), and transfer the specimen to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 L) and start the timer. See illustration below. Avoid trapping air bubbles in the specimen well (S). For Whole Blood (Venipuncture/Fingerstick) Specimens: To use a dropper: Hold the dropper vertically, draw the specimen 0.5-1 cm above the Fill Line, and transfer 1 drop of whole blood (approximately 10 µL) to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 uL) and start the timer. See illustration below. To use a micropipette: Pipet and dispense 10 µL of whole blood to the specimen well (S) of the test device, then add 3 drops of buffer (approximately 90 µL) and start the timer. See illustration below. 3.Wait for the colored line(s) to appear. Read results at 10 minutes. Do not interpret the result after 20 minutes.
We have just achieved a major breakthrough in the development of dengue igg/igm antibody early test. Our new product is capable to detect the presence of dengue igm antibody in human serum within 3-5 days since primary infection (tested and verified with reference standard blood sample from usa cdc), while similar products currently found on the market can only detect it after at least 10-15 days. The significance of this achievement is that the new dengue igg/igm antibody early test now can diagnose dengue infection at a very early stage, which previously could only be done with a dengue ns1 antigen test. Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 95.3% Specificity: 95.0% Specimen: whole blood/serum/plasma .
CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 �µL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)
CAT No : R0063C. Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes Duo test format minimizes processing time IgM detection indicates recent infection IgG detection indicates recent or previous infections Ag detection indicates a current infection Individually sealed foil pouches containing: One cassette device One desiccant 5 uL Capillary tubes (for Dengue IgG/IgM test) Plastic droppers (for Dengue Ag test) Sample diluent (REF SB-R0062, 5 mL/bottle) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit 30 Brand : CTK BioTech Result Time (Rapid Kits) :20-25 Min Sample Material :Serum / Plasma / Whole Blood Cat. No : R0061c The OnSite Dengue IgG/IgM 3.0 Combo Rapid Test is a lateral flow immunoassay for the simultaneous detection and differentiation of IgG and IgM antiâ??dengue virus (DEN1, 2, 3 and 4) in human serum, plasma or whole blood. Product Features: Utilizes recombinant chimeric dengue virus licensed from the US CDC Detects all four dengue serotypes IgM detection indicates recent infection IgG detection indicates recent or previous infections Each kit contains: Individually sealed foil pouches containing: One cassette device One desiccant 5 AUL Capillary tubes Sample diluent (REF SB-R0061, 5 mL/bottle) One package insert (instruction for use)
CE marked Dengue virus IgG/IgM rapid test Assay+ Dengue IgG/IgM antibody rapid test is manufactured in Canada to detect specific dengue IgG and IgM for the healthcare providers. Assay+ dengue IgG/IgM Rapid Test Kit is qualitative test device for dengue virus IgM/IgG antibodies in human serum, plasma, whole blood or finger tip blood. This device has been authorized by CE Mark. Sensitivity over 90% for IgM and IgG and 100% specificity have been proved used by our customers in large quantity.
SARS-CoV-2 Rapid Antigen Test kit Colloidal Gold Method Medical Simple Rapid Convenient Sensitivity : 98.4% Specificity : 98.1% Test Time : 10-15min
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing. 1.Easy to collect samples simple operation without professional equipment. 2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy. 4.Suitable for large-scale rapid screening. Shelf life: 24 Months Test Result time: 10 Mins Packing: 25 Pieces per Box
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Saliva Test Kit Painless testing plastic disposable Ag Rapid Detection Kit
Specification Strength/ Size Packing Size Packed In Filariasis Kit Includes One test Strip, Desiccant and Dropper 50 Strip Test Per Pack 50 Box Pack
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.
Monkeypox IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a solid phase immunochromatographic assay for the rapid, qualitative and differential detection of IgG and IgM antibodies to monkeypox virus in human whole blood, serum or plasma. This test provides only a preliminary test result.
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
