Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : CTK BioTech Sample : serum or plasma Storage : 2 - 8 C Cat No : AE0610 INTENDED USE: The TRUSTwell Syphilis Ab kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of antibodies (IgG, IgM, IgA) against Treponema pallidum (Tp) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with Tp. Any reactive specimen with the TRUSTwell Syphilis Ab ELISA Test must be confirmed with alternative testing method(s) and clinical findings. TEST PRINCIPLE: The TRUSTwell Syphilis Ab ELISA Test is a solid phase enzyme linked immunosorbent assay based on the principle of the double antigen sandwich technique for the detection of antibodies to Tp in human serum or plasma. The TRUSTwell Syphilis Ab ELISA Test is composed of two key components: 1) Solid microwells pre-coated with recombinant Tp antigens; 2) Liquid conjugates composed of recombinant Tp antigens conjugated with horseradish peroxidase (HRP-Tp conjugates). During the assay, the test specimen and HRP-Tp conjugates are incubated simultaneously with the coated microwells. Antibodies (IgG, IgM, or IgA) to Tp if present in the specimen, reacts to the Tp antigens coated on the microwell surface as well as the HRP-Tp conjugates, forming sandwich complex conjugates. Unbounded conjugates are then removed by washing. The presence of the complexed conjugates is shown by a blue color upon additional incubation with TMB substrate. The reaction is stopped with Stop Solution and absorbances are read using a spectrophotometer at 450 /620-690 nm. Clinical Performance: A total of 1132 patient specimens from susceptible subjects were tested by the TRUSTwell Syphilis Ab ELISA Kit. Relative Sensitivity:100%, Relative Specificity:99.8%, Overall Agreement:99.82%.
Elisa kit Available in Various Parameters mainly HIV1, 2, HCV, HBs Ag In 36,48,96 tests packing
Product Details: Number of Reactions(Preps)/Kit ; 96 wells Brand : Abbott Test Type : Elisa CAT No : E-LEP01M / E-LEP01M05 The Panbio Leptospira IgM ELISA is for the qualitative detection of IgM antibodies to leptospira in serum as an aid in the clinical laboratory diagnosis of patients with clinical symptoms consistent with leptospirosis.
Product Details: Number of Reactions(Preps)/Kit :20T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15min CAT No : RK012-20 One step, rapid, immunochromatographic test for the detection of Dengue IgMlIgG antibodies to four senatypes of dengue virus (DEN-I, DEN-2. DEN-3 and DEN-4) in human serum, plasma or whole blood. Kit Contents: Standard Q Dengue IgM IgG cassette x 20 Specimen transfer device 10ml x 20 Butter bottle 4ml x 01 Instructions for use x 1 STANDARD Q Dengue IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting IgM and IgG specific to Dengue virus, the primary and secondary Dengue virus infections can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity. Advantage: Differential detection of IgG and IgM antibodies Easy to use, Easy to read and interpret Room temperature storage Able to read positive/negative infections fast and accurately with a little amount of sample (10 �µl)
Product Details: Number of Reactions(Preps)/Kit : 96wells Brand : Abbott Cat. No : 01PE10 The Panbio Dengue IgG Capture ELISA is used to detect elevated IgG antibodies to dengue virus (serotypes 1-4) in patients with secondary infection. This test is intended as an aid in the clinical laboratory diagnosis.
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : Abbott Product Type : Microplate Sample : Serum CAT. NO : 11EK50 The presence of circulating non-structural glycoprotein (NS1) indicates Viremia. If sufficient virus is present, NS1 can be detectable in a patientâ??s blood from day 0 to day 5 following disease onset. The detection of NS1 antigen is therefore useful as a test of early acute infection. â?¢ Early diagnosis of dengue infection High accuracy with all dengue serotypes (DEN1,2,3, and 4) Simple and easy to use: All necessary reagents included in the kit â?¢ Shelf life and storage temperature: 18 months from the date of manufacturing at 2-8 'C Performance: Sensitivity 93.3 % (87.4 - 96.6 %), Specificity 98.9 % (96.0 - 99.7 %)
Product Details: Number of Reactions(Preps)/Kit : 50T Brand : SD Biosensor ICMR Approved : Yes Result Time (Rapid Kits) : 15 min Sample Type : Blood Country of Origin : Made in India STANDARD E Dengue NS1 Ag ELISA analyzes Dengue NS1 antigens in serum and plasma using enzyme linked immunosorbent assay. Simple and easy to use: All necessary reagents included in the kit Highest accuracy with all dengue serotypes(DEN1,2,3, and 4) Able to detect antigens in samples with high sensitivity and specificity Performance Sensitivity : 91.4% (181/198) / Specificity : 98.2% (221/225)
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
The Toxoplasma gondii IgM GENLISA ELISA is intended for the qualitative determination of Toxoplasma gondii IgM antibody in human serum and plasma. Pack Size - ELISA 96 wells
The Rubella IgM GENLISATM ELISA is intended for the qualitative determination of Rubella Virus IgM class antibodies in human serum and plasma. Pack Size - ELISA 96 wells
The CMV IgM GENLISA ELISA is intended for the qualitative determination of CMV IgM in human serum and plasma. ELISA 96 wells
The HEV IgM GENLISA ELISA is intended for the qualitative determination of Hepatitis E Virus IgM in human serum and plasma.
Dengue rapid test kit.
The FactView Dengue IgG/IgM Antibody Combo test is a diagnostic assay used for the simultaneous detection of both IgG and IgM antibodies produced by the immune system in response to dengue virus infection. Here's more information about this type of diagnostic test: Purpose: The test is used for the diagnosis of dengue virus infection in patients presenting with symptoms consistent with dengue fever or other dengue-related illnesses. Dengue is a mosquito-borne viral infection caused by four closely related viruses (DENV-1, DENV-2, DENV-3, and DENV-4) transmitted by Aedes mosquitoes. Principle: The FactView Dengue IgG/IgM Antibody Combo test is an immunochromatographic assay that detects the presence of both 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 and provide long-term immunity. Components: The test typically 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. 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. 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 Dengue IgG/IgM Antibody Combo test demonstrates high sensitivity and specificity for detecting dengue virus infection. 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 dengue virus provides valuable information for diagnosing acute or recent dengue virus infection, determining immune status, and guiding patient management decisions.
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)
Product Description FDA EUA, CE Price of product ( USD price or FOB price) : "10,000-99,999: $8.45 100,000-249,999:$7.98 250,000-499,999: $7.78 500,000+: Contact" Product origin : China Minimum Order Size and Packgaing details : 10,000 Individual tests (25/box)
1. Principle This test kit is based on the competitive enzyme immunoassay for the detection of Gentamicin in the sample. The coupling antigen is pre-coated on the micro-well stripes. The Gentamicin in the sample and pre-coated coupling antigen on the micro-well stripes compete for the anti-Gentamicin antibody. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the sample has a negative correlation with the Gentamicin in it. The value is compared to the standard curve and the Gentamicin concentration is subsequently obtained. 2. Technical specifications Sensitivity: 0.05 ppb Incubator temperature: 25 Incubator time: 30minï½?15min
1. Principle This test kit is based on the competitive enzyme immunoassay for the detection of Florfenicol in samples. The coupling antigens are pre-coated on the micro-well stripes. The Florfenicol in the sample and the conjugate antigens pre-coated on the micro-well stripes compete for the anti-Florfenicol antibodies. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value has a negative correlation with the Florfenicol concentration in the sample. This value is compared to the standard curve and the Florfenicol concentration is subsequently obtained. 2. Technical specifications Sensitivity: 0.1 ppb Incubator temperature: 25 Incubator time: 30minï½?15min
1. Principle This test kit is based on the competitive enzyme immunoassay for the detection of Tylosin in the sample. The coupling antigens are pre-coated on the micro-well stripes. The Tylosin in the sample and the coupling antigens pre-coated on the micro-well stripes compete for the anti-Tylosin antibody. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the sample has a negative correlation with the Tylosin in it. This value is compared to the standard curve and the Tylosin concentration is subsequently obtained. 2. Technical specifications Sensitivity: 0.5 ppb Incubator temperature: 25 Incubator time: 75 min
The kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Human Androgen in samples. Add Androgen to monoclonal antibody Enzyme well which is pre-coated with Human Androgenmonoclonal antibody, incubation; then, add Androgenantibodies labeled with biotin, and combined with Streptavidin-HRP to form immune complex; then carry out incubation and washing again to remove the uncombined enzyme. Then add Chromogen Solution A, B, the color of the liquid changes into the blue, And at the effect of acid, the color finally becomes yellow. The chroma of color and the concentration of the Human Substance Androgen of sample were positively correlated. Standard; 128nmol/L.
