Product Details: Brand : Boditech Med Incorporated Size : 25 T Specimen : human serum/plasma Specimen volume : 50 Microliter Cat. No. : CFPC-47 INTENDED USE : ichromaâ?¢ Vitamin D is a fluorescence Immunoassay (FIA) for the quantitative determination of total 25(OH)D2/D3 level in human serum/plasma. It is useful as an aid in management and monitoring of regulating the concentration of calcium and phosphate in the bloodstream and promoting the healthy growth and remodeling of bone.For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the target material in the sample binds to the fluorescence (FL)-labeled detection antibody in detection buffer, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of 25(OH)D3 and bovine serum albumin (BSA) is immobilized on a test strip, and interferes with the binding of target material and FL-labeled antibody. If the more target material exists in blood, the less detection antibody is accumulated, resulting in the less fluorescence signal. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. The releasing buffer dispensed in a vial is stable for 20 months if stored at 2-8 C. Opened detection buffer and releasing buffer are stable for 12 months at 2-8 C if kept capped in original container and free from contaminations. After the cartridge pouch is opened, the test should be performed immediately. MATERIALS SUPPLIED : REF CFPC-47Components of ichroma Vitamin D Cartridge Box:- Cartridges 25- Sample Mixing Tubes 25- ID Chip 1- Instruction For Use 1 Detection Buffer Vial (3 mL) 1 Releasing Buffer Vial (2 mL) 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human whole blood/serum/ plasma Sample volume : 50 Microliter stored at 4 - 30 DegreeC Cat No : CFPC-65 Troponin I (Tn-I) Plus Early diagnosis of myocardial infarction with high sensitivity Troponin I (Tn-I) Plus can diagnose myocardial infarction and myocardial necrosis at an early stage with high sensitivity by accessing Tn-I level in the blood, thus can help prevent progression to more severe cases. INTENDED USE: ichroma Tn-I Plus is a Fluorescence Immunoassay (FIA) for the quantitative determination of cardiac troponin-I (Tn-I) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of acute myocardial infarction (AMI). For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show Tn-I concentration in the sample. MATERIALS SUPPLIED : REF CFPC-65 Components of ichroma Tn-I Plus Cartridge Box: - Cartridge 25 - 50L Capillary tube 25 - ID chip 1 - Instruction for Use 1 Buffer Box For ichorma II - Detector (Capped with plastic lid) 25 - Diluent 1 For ichroma 50 - Detector (Sealed with aluminum foil) 25 - Diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human whole blood/ serum/ plasma/control Specimen volume : 10 Microliter stored at 4 - 30 DegreeC Cat No : CFPC-77 NT-proBNP Helping to diagnose heart diseases and evaluate the severity level BNP and NTproBNP are peptides that are continuously produced in the heart. When the muscles in the left ventricle over-stretch as in heart failure, the secretion of these peptides into blood increases. One may utilize the level of NTproBNP in blood to assess the cardiac event and its severity. Both of BNP and NTproBNP can be used to show different aspects of the heart failure. INTENDED USE: ichroma NT-proBNP is a fluorescence Immunoassay (FIA) for the quantitative determination of NT-proBNP in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of persons suspected of having congestive heart failure. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto the nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show NT-proBNP concentration in the sample. MATERIALS SUPPLIED : REF CFPC-77 Components of ichroma NT-proBNP Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Buffer Box For ichroma - Detector tube 25 - Detector diluent 1 For ichromaâ?¢-50 - Detector tube 25 - Detector diluent 1
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : human whole blood/serum/plasma Specimen volume : 5 Microliter stored at 4-30 C Cat No : CFPC-51 Anti-CCP Plus Supporting to distinguish and diagnose rheumatoid arthritis This test helps to diagnose and provide appropriate treatment for chronic systemic autoimmune diseases and rheumatism by quantifying Anti-CCP in the blood. INTENDED USE : ichroma Anti-CCP is a fluorescence Immunoassay (FIA) for the qualitative or semi-quantitative determination of human IgG autoantibodies to cyclic citrullinated peptides (CCP) in human whole blood/serum/plasma. It is useful as an aid in the diagnosis of rheumatoid arthritis (RA) in combination with other clinical and laboratory findings. For in vitro diagnostic use only. STORAGE AND STABILITY : The cartridge is stable for 20 months (while sealed in an aluminum foil pouch) if stored at 4-30 C. The detection buffer dispensed in a tube is stable for 20 months if stored at 2-8 C. After the cartridge pouch is opened, the test should be performed immediately. PRINCIPLE : A synthetic cyclic citrullinated peptide (CCP) is immobilized on a porous membrane. After a sample is added to the sample port, detection buffer, consisting of fluorescent conjugated polyclonal antibody to human IgG, is loaded to the buffer port. The more anti-CCP antibodies in sample forms the more the peptide antigen/anti-CCP antibodies complex and leads to stronger intensity of fluorescence signal on detector anti-human IgG, which is processed by instrument for ichroma tests to show anti-CCP level in sample. MATERIALS SUPPLIED : REF CFPC-51 Components of ichroma Anti-CCP Cartridge Box: - Cartridges 25 - Sample collectors 25 - ID Chip 1 - Instruction For Use 1 Box containing Detection Buffer Tubes - Detection Buffer Tubes 25
Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples: human whole blood/serum/ plasma Specimen volume : 50 microliter stored at 4 - 30 C Cat No : CFPC-91 Total IgE Assessing to diagnose acute allergic diseases This test assesses IgE in blood to support diagnosing of acute allergic diseases. INTENDED USE : ichroma Total IgE is a fluorescence immunoassay (FIA) for the quantitative determination of total IgE in human whole blood/serum/ plasma. It is useful as an aid in diagnosis and management of allergic disease. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichroma tests to show total IgE concentration in the sample. MATERIALS SUPPLIED : REF CFPC-91 Components of ichroma Total IgE Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box - Detection Buffer 25
Product Details: Brand : Boditech Med Incorporated Size ; : 25 T Samples : Human whole blood/plasma/control Specimen volume : 10 Microliter Storage : 4- 30 DegreeC Cat No : CFPC-25 D-Dimer Measuring D-dimer level in 12 mins The presence of D-dimer in blood indicates that thrombin has been formed and fibrin generated from fibrinogen in vivo as a result of activation of the coagulation system. This test measures the level in the blood to help assess the thrombotic state. INTENDED USE : ichroma D-Dimer is a fluorescence Immunoassay (FIA) for the quantitative determination of D-Dimer in human whole blood/plasma. It is useful as an aid in management and monitoring of post therapeutic evaluation of thromboembolic disease patients. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show D-Dimer concentration in the sample. MATERIALS SUPPLIED : REF CFPC-25 Components of ichroma D-Dimer Cartridge Box: - Cartridge 25 - ID chip 1 - Instruction for use 1 Box containing Detection Buffer tubes - Detection buffer 25
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 75 Microliter Sample : serum/plasma/control Storage Temperature : 4-30 DegreeC. Cat No : CFPC-27 Prolactin (PRL) Assessing to diagnose hypothalamic impairments & pituitary disorders This test helps select and diagnose mammary gland development, infertility treatment and pituitary diseases by quantifying blood PRL. INTENDED USE : ichroma PRL is a fluorescence Immunoassay (FIA) for the quantitative determination of Prolactin (PRL) in human serum/plasma. It is useful as an aid in management and monitoring of hypothalamic-pituitary disorders. For in vitro diagnostic use only. PRINCIPLE: The test uses a sandwich immunodetection method; the detector antibody in buffer binds to antigen in sample, forming antigen-antibody complexes, and migrates onto nitrocellulose matrix to be captured by the other immobilized-antibody on test strip. The more antigen in sample forms the more antigenantibody complex and leads to stronger intensity of fluorescence signal on detector antibody, which is processed by instrument for ichromaâ?¢ tests to show PRL concentration in sample. MATERIALS SUPPLIEED : REF CFPC-27 Components of ichroma PRL Cartridge Box: - Cartridges 25 - ID Chip 1 - Instruction for Use 1 Detection Buffer Box: - Detection Buffer tubes 25
Product Details: Number of Reactions(Preps)/Kit : 25 T Brand : Boditech Med Incorporated Sample Volume : 10 Microliter Sample : Human whole blood/serum/ plasma/control Reaction Time : 3 mins Cat No : ichroma CRP-25 CRP Assessing to diagnose infection and inflammation This test can help with proper prescription and treatment by quickly and accurately measuring CRP with a finger-tip blood. INTENDED USE : ichroma CRP is a fluorescence Immunoassay (FIA) for the quantitative determination of CRP in human whole blood/serum/ plasma. It is useful as an aid in management and monitoring of autoimmune diseases and infectious processes, such as rheumatoid arthritis. For in vitro diagnostic use only. PRINCIPLE : The test uses a sandwich immunodetection method; the detector antibodies in buffer bind to antigens in the sample, forming antigen-antibody complexes, and migrate onto nitrocellulose matrix to be captured by the other immobilized-antibodies on test strip. More antigens in the sample will form more antigen-antibody complexes which lead to stronger fluorescence signal by detector antibodies, which is processed by instrument for ichromaâ?¢ tests to show CRP concentration in the sample. MATERIALS SUPPLIED : REF i-CHROMA CRP-25 Components of ichrom CRP Cartridge Box: - Cartridge 25 - ID Chip 1 - Instruction for Use 1 - Sample Collector 25 Box containing Detection Buffer - Detection buffer 25
Product Price: Rs 53,000 / Unit Product Details: Capacity(Litre per minute) 5 LPM Brand Philips Oxygen Concentration 93 +/- 3 % Sound Level 45 (typical) dB Weight (in kg) 14 kgs Dimension 58.4 cm H x 38.1 cm W x 24.1 cm D (23" H x 15" W x 9.5" D) Alarm Low Oxygen (82%) and Very Low Oxygen (70%) I Deal In New Only Input Voltage 120 +/- 10% VAC Input Frequency 60 Hz Until now, oxygen concentrators have been very similar - heavy, bulky, noisy, or requiring frequent maintenance. EverFlo from Respironics is a unique stationary concentrator that delivers what homecare providers want and patients deserve. Features: Lightweight for easy transport The EverFlo Oxygen concentrator weighs in at only 31 pounds, reducing shipping and storage costs and risk of injury. Compact design looks less like a medical machine EverFlo's ergonomic design takes up less space and doesn't draw as much attention. The Right Fit series focuses on patients' needs EverFlo is part of the Right Fit, a complete portfolio of oxygen products and programs inspired by patients and built for business. Low maintenance for reduced service costs No homecare provider filter change for two years. Patients do not ever have to change filters. Lower power consumption makes EverFlo patient-friendly The system uses less electricity and produces less heat. Humidifier Bottle Platform for extra flexibility The platform is designed to be compatible with all bottle styles and features an easy-to-use velcro closure. Recessed flow meter reduces accidental breakage Recessed flow meter reduces accidental breakage Oxygen purity indicator option for increased security EverFlo is available with or without oxygen purity indicator. This OPI (Oxygen Percentage Indicator) ultrasonically measures oxygen output as a purity indication.
Thermofisher Quantstudio 5 Real Time PCR System, 96 wells Product Details: Model Name/Number QuantStudio 5 Includes Desktop Brand Thermofisher Sample Capacity/Format 96 wells Volume Thermal Block Sample 0.2ml Block Format Non-Interchangeable Display Type Touch Screen Smaller foot print 27x50x40 cm CAT No : A28139 Features: Proven OptiFlex technology (6 decoupled channels/21 filter combinations with white LED) for trusted results User account management, locked workflow, and Pause features for greater control of experiment data Built-in software features to support compliance with 21 CFR Part 11 guidelines Secure cloud-based software provides increased accessibility and storage options Simplified instrument software with interactive touchscreen for greater ease of use The Applied Biosystems QuantStudio 5 Real-Time PCR System for Human Identification with tower computer is the latest addition to our human identification (HID) real-time PCR family of products. This instrument is designed for both new and experienced users who need a simple, reliable, and affordable real-time PCR system that doesnâ??t require compromise on performance or quality. When used with our latest advances in quantification chemistry and HID Real-Time PCR Analysis Software, this system offers a sensitive, robust solution for forensic DNA quantification. It also helps prepare laboratories for future quantification technologies. With maximum dye versatility, this HID solution offers accurate, trusted results in a small benchtop footprint
Product Details: Number of Reactions(Preps)/Kit 30T Brand CTK Biotech Result Time (Rapid Kits) 20mins Test Type Rapid Test CAT No : R0234C The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
Quantstudio 3 Real Time Pcr System, 0.2 mL, 96 wells Product Details: Brand Thermofisher Model Name/Number QuantStudio 3 Sample Capacity/Format 96 wells Volume Thermal Block Sample 0.2 mL Weight 25 kg CAT No : A28137 Features: Simplified instrument software with interactive touchscreen for greater ease of use Proven OptiFlex technology (4 coupled channels with white LED) for trusted results Secure cloud-based software option provides increased accessibility and storage options User account management, locked workflow, and Pause features for greater control of experiments
Product Details: Number of Reactions(Preps)/Kit 30 T Brand SD Biosensor ICMR Approved Yes Result Time (Rapid Kits) 10 Min Cat. No RK033-30 General Description: STANDARD Q HIV/Syphilis Combo Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O, HIV 2 and Syphilis (Treponema pallidum) in human serum, plasma or whole blood. The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection for HIV or Syphilis infected patients, patients with signs and symptoms (HIV and Syphilis) and persons at risk. The test is able to quick screen the HIV/syphilis infection and gives the advantage of managing these two diseases at the same time. Technical specifications: Technology: Rapid chromatographic immunoassay. Format: Test cassette, 25 tests. Sample type: serum/plasma/venous whole blood specimen Sample volume: Serum Plasma 10�µl/whole Blood 20 µl. Sensitivity: HIV 100% & Syphilis 98.8% Specificity: HIV 99.9%/syphilis 100%/ Time to result: Minimum of 15 minutes.
Sysmex 3-part XP 300 Differential Automated Hematology Analyzers Product Details: Automation Fully Automatic Instrument Name Haematology Analyzer Brand Sysmex Differential Type 3-Part Sample Volume Whole blood mode: 50 Microliter Parameters Whole blood mode: 8 parameters with 3-part Differential WBC; RBC; HGB; HCT; MCV; MCH; MCHC; PLT; Sysmex provides two 3-part WBC Differential automated hematology analyzers*. These systems are ideally suited for physician office laboratories, clinics and small hospitals that perform moderately complex testing. Built on reliable Sysmex technology, the 3-part differential analyzers feature simple operation, minimal maintenance and compact, space-saving designs. With its simplified operation, the XP-300 is ideal for clinics, satellite laboratories and research testing. The XP-300 provides a CBC with 8 parameters, including a 3-part WBC Differential with an absolute neutrophil count (ANC).
Product Details: Number of Reactions(Preps)/Kit 25 Test Brand SD Biosensor Result Time (Rapid Kits) 15 Min Cat. No 09LEP10D STANDARD Q Leptospira IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Leptospira interrogans in serum, plasma and whole blood using immunochromatography. Screening test results can be obtained within 15 minutes with high sensitivity and specificity. Advantage Differential detection of IgG and IgM antibodies Easy to use, Easy to read and interpret Room temperature storage of 2-40 / 36-104 Able to read positive/negative infections fast and accurately with a little amount of sample (10 µl).
Product Details: Brand RAPHA CAT No : N116A Size 50 T Result Time 5 Min UNIQUE FEATURES: EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
Product Details: Number of Reactions(Preps)/Kit 10 T Brand CTK BioTech Test Type Rapid test Sample human serum, plasma, or whole blood Test time 10 Min Cat No : R0253C The OnSite TORCH Panel Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies (IgG and IgM) to Toxoplasma gondii (T. gondii), rubella virus, cytomegalovirus (CMV), herpes simplex virus 1 (HSV-1), and herpes simplex virus 2 (HSV-2) in human serum, plasma, or whole blood. This test is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with T. gondii, rubella virus, CMV, HSV-1 and HSV-2. Any interpretation or use of this preliminary test result must also rely on other clinical findings as well as on the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device. Recommended for use: Any person presenting with clinical signs or symptoms consistent with TORCH infection. Women who are pregnant or who are planning to become pregnant Individuals with a compromised immune system The OnSite TORCH Panel Rapid Test detects and differentiates IgG and IgM antibodies for all 5 TORCH infections. In general, a negative test result indicates that the individual is at risk for acquiring a primary infection. A positive IgM result only indicates acute infection, a positive IgM and IgG test indicate acute, late phase infection, and a positive IgG test result only indicates past or chronic infection. The presence of IgM anti-rubella virus or high titers of IgG anti-rubella virus (> 200 IU/mL) are suggestive of acute rubella infection. Lower titers of IgG anti-rubella virus (â?¥ 10-15 IU/mL) are suggestive of previous exposure and protective immunity. An individual with an IgG anti-rubella virus titer less than 10-15 IU/mL is considered to be at risk of acquiring a rubella virus infection. The TORCH Panel Rapid test also differentiates between HSV-1 and HSV-2 antibodies using HSV-1 specific glycoprotein G1 and HSV-2 specific glycoprotein G2. Product Specification : Individually sealed foil pouches containing: One cassette device Two desiccants Plastic droppers Sample diluent (REF SB-R0253, 5 mL/bottle) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit 30 T Brand CTK BioTech Result Time (Rapid Kits) 10 Min Sample Material Plasma/Serum Test Type Rapid test Cat. No R0310C The OnSite RF Rapid Test is a lateral flow immunoassay for the qualitative detection of all subtypes of rheumatoid factor (RF) in human serum, plasma or whole blood at a sensitivity of 8 IU/ml. Product Features : Rapid test to make RF detection simpler and quicker than Latex Detects RF levels as low as 8 IU/mL Detects all RF isotypes including IgM, IgG, and IgA Simple procedure minimizes risk of operator error â?? no sample preparation required. The results are ready in 10 minutes, which increases diagnostic efficiency. The least complicated RF test- can be performed in any setting by any health care provider with simple training Rapid test format allows room temperature shipping and storage. Each kit contains: Individually sealed foil pouches containing: One cassette device One desiccant Capillary tubes (5 µL) Sample Diluent ( REF SB-R0310, 5 mL/bottle ) One package insert (instruction for use)
Product Details: Number of Reactions(Preps)/Kit 30T Brand CTK BioTech ICMR Approved Yes Result Time (Rapid Kits) 20min CAT No : AR5001C Details : Utilizes Recombinant Orientia tsutsugamushi antigens. Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus) Compatible with Whole blood, Serum and Plasma. Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%. Results in 20 minutes. Each kit contains: Individually sealed foil pouches containing: One cassette device One desiccant Detection buffer (tris-based buffered solution with preservatives) Instructions for Use
Product Details: Brand J.Mithra Test Kit Type: Dengue Test Kit (Rapid) Sensitivity & Specificity High Shelf Life: 30 months at 2-30 DegreeC Pack Size: 10, 30 & 50 Tests Cat. No IR028010 Intended Use : Dengue Day 1 Test is a rapid solid phase immuno-chromatographic test for the qualitative detection of Dengue NS1 Antigen and differential detection of IgM and IgG antibodies to Dengue virus in Human serum/plasma. This test is for in vitro diagnostic use only and is intended as an aid in the earlier diagnosis of Dengue infection & presumptive diagnosis between primary and secondary Dengue infection. Salient Features: First line testing kit for detecting dengue infection from day 1 using NS1 Antigen & differential detection of IgM & IgG Antibodies. Diagnosis of both Primary & Secondary Infection. Detection of all the 4 Dengue serotypes (DEN-1, DEN-2, DEN-3 and DEN-4). Highly Sensitive & Highly Specific Long shelf life: 30 months at 2-30 C. Convenient pack sizes: 10 Tests, 30 Tests & 50 Tests. Principle:Dengue Day 1 test kit consists of two devices: one device for detection of Dengue NS1 antigen and second device for the differential detection of Dengue IgM/IgG antibodies in Human serum/plasma. Dengue NS1 Antigen device contains two lines; (Control line) & T (Dengue NS1 Antigen test line). Test line is coated with anti-dengue NS1 Ag. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloidal conjugate making antigen antibodies complex. This complex migrates along the membrane to the test region and forms the visible pink line at as antibody-antigen-antibody gold colloid forms. Dengue IgM/IgG test device contains three lines; C (Control line), M (IgM test line) & G (IgG test line).IgM test line is coated with anti-human IgM and IgG test line is coated with anti-human IgG.When a sample is added to the device, IgG and IgM antibodies in the sample react with anti-human IgM or IgG antibodies coated on the membrane respectively. Colloidal gold complexes containing dengue 1-4 antigens is captured by the bound anti-dengue IgM or IgG on respective test bands located in the test window causing a pale to dark red band to form at the IgG or IgM region of the test device window. The intensity of the test bands in the respective device will vary depending upon the amount of antigen /antibody present in the sample. The appearance of any pink/ red colour in a specific test region should be considered as positive for that particular antigen and/or antibody type (IgG or IgM). A red procedural control line should always develop in the test device window to indicate that the test has been performed properly Dengue NS1 Ag : Sensitivity 96% and Specificity 98%. Dengue IgM/IgG Antibody test : Sensitivity 95% and Specificity 97%.
