Ichroma D Dimer Test

General Information One-Step the D-Dimer Rapid Test Device is a chromatographic immunoassay for the qualitative detection of D-Dimer in human blood. Specimen : Serum, Plasma or Whole Blood Reading Time : 10 -15min

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

Specimen:Whole Blood /Serum / Plasma D-Dimer Rapid Test Device is used for the qualitative detection of D-dimer in human whole blood and plasma; The test is used as an aid in the assessment and evaluation of patients with suspected disseminated intravascular coagulation (DIC), deep vein thrombosis (DVT), and pulmonary embolism (PE). During blood coagulation process, fibrinogen is converted to fibrin by the activation of thrombin. The resulting fibrin monomers polymerise to form a soluble gel of non-cross-linked fibrin. This fibrin gel is then converted to cross-linked fibrin by thrombin activated Factor XIII to form an insoluble fibrin clot. Production of plasmin, the major clot-lysing enzyme, is triggered when a fibrin clot is formed. Although fibrinogen and fibrin are both cleaved by the fibrinolytic enzyme plasmin to yield degradation products, only degradation products from cross-linked fibrin contain D-dimer and are called cross-linked fibrin degradation products. Therefore, fibrin derivatives in human blood or plasma containing D-dimer are a specific marker of fibrinolysis. The D-Dimer Rapid Test Device (Whole blood//Plasma) detects D-Dimer through visual interpretation of color development in the internal strip. Anti-D-Dimer antibodies are immobilized on the test region of the membrane, and anti-mouse antibodies immobilized on the control region. During testing, the specimen reacts with anti-D-Dimer antibodies conjugated to colored particles and precoated onto the sample pad of the strip. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient D-Dimer in the specimen, a colored band will form at the test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.

Cardiovascular series 100-10000ng/ml Plasma/Whole blood Plasma100ul Whole blood120ul 15Min.

Tuna Fish Oil is one of the richest known sources of DHA, which plays a central role in the development of the brain and the central nervous system. Scientific studies have shown that children receiving an ample supply of DHA perform better on intelligence tests than do those who lack sufficient DHA in their diets. Following is the standard specification, which can be amended to meet customer's requirements. Product no. HT403 Tuna Fish Oil Pale yellow oil is produced from fresh tuna. It is refined and deodorized. 200 ppm natural tocopherols are added to the oil. The Tuna fish oil complies with EU legislation on contaminants in foodstuffs. The Tuna fish oil can be fortified with vitamins A, D and E, antioxidants and flavors. The Tuna fish Oil is packed under nitrogen and can be delivered in drums, IBC, flexitanks or tank containers

The FactView Vitamin D Rapid Test Device is a diagnostic assay used for the qualitative detection of Vitamin D levels in blood samples. Here's more information about this type of diagnostic test: Purpose: The test is used for the rapid detection of Vitamin D deficiency or insufficiency. Vitamin D is essential for bone health, immune function, and various other physiological processes in the body. Principle: The FactView Vitamin D Rapid Test Device is typically an immunochromatographic assay that detects the presence of Vitamin D in a patient's blood sample. The test device contains specific antibodies or receptors that bind to Vitamin D molecules, leading to the formation of visible test lines. Components: The test kit usually includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific reagents for capturing Vitamin D molecules. 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 a few minutes. Interpretation: The appearance of colored lines on the test strip indicates the presence or absence of Vitamin D in the blood sample. A visible line in the control region indicates that the test is valid. Additional lines in the test region(s) indicate positive results for Vitamin D. Sensitivity and Specificity: The FactView Vitamin D Rapid Test Device demonstrates sensitivity and specificity for detecting Vitamin D levels within a certain range. 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 Vitamin D levels provides valuable information for assessing Vitamin D status, identifying deficiency or insufficiency, and guiding patient management decisions. Vitamin D deficiency is associated with various health problems, including bone disorders, immune dysfunction, and increased risk of certain diseases. Limitations: While rapid diagnostic tests are useful for Vitamin D screening, they have limitations compared to more accurate laboratory methods such as liquid chromatography-mass spectrometry (LC-MS). Factors such as test sensitivity, specificity, and the influence of interfering substances can affect test performance. Overall, the FactView Vitamin D Rapid Test Device is a convenient tool for assessing Vitamin D levels, allowing for timely intervention and management of Vitamin D-related health conditions. However, results should be interpreted carefully in conjunction with clinical evaluation and other laboratory tests.

Product Details: Brand : Boditech Med Incorporated Size : 25 T Samples : Human serum/plasma/ control Specimen volume : 75 Microliter stored at ; 4 - 30 DegreeC Cat No ; CFPC-44 T3 Assessing to diagnosis & to monitor thyroid diseases(T3) This test assesses the level of T3 in the blood to diagnose thyroid dysfunction, help to receive appropriate treatment, and help to confirm the treatment effect through periodic measurement. INTENDED USE : ichroma T3 is a fluorescence Immunoassay (FIA) for the quantitative determination of triiodothyronine (total T3) in human serum/plasma. It is useful as an aid in management and monitoring of determination of thyroid disorders. For in vitro diagnostic use only. PRINCIPLE : The test uses a competitive immunodetection method. In this method, the analyte in the sample binds to the fluorescence labeled (FL) 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 T3 and bovine serum albumin (BSA) is immobilized and interferes with the binding of analyte and fluorescence labeled (FL) antibody. If more analytes exist in the sample, less detection antibodies are accumulated, resulting in less fluorescence signal. MATERIALS SUPPLIED : REF CFPC-44 Components of ichroma T3 Cartridge Box: - Cartridge 25 - Detector tube 25 - Detector diluent 2 - ID chip 1 - Instruction for Use 1

Product Details: Brand : Boditech Med Incorporated Size : 25 T Specimen : Human serum/plasma/ control Specimen volume : 75 microliter stored at 4 - 30 DegreeC. Cat No : CFPC-26 T4 Assessing to diagnosis & to monitor thyroid diseases(T4) Thyroxine (T4) is a type of thyroid hormone. An abnormal amount of T4 may indicate thyroid disease. The T4 test measures total T4, including T4 bonded to protein and free T4. A T4 test will help determine what type of problem is affecting the thyroid. INTENDED USE : ichroma T4 is a fluorescence Immunoassay (FIA) for the quantitative determination of thyroxine (T4) in human serum/plasma. It is useful as an aid in management and monitoring of thyroid disorder. 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 detector, to form the complex as sample mixture. This complex is loaded to migrate onto the nitrocellulose matrix, where the covalent couple of T4 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. MATERIALS SUPPLIED : REF CFPC-26 Components of ichroma T4 Cartridge Box: - Cartridges 25 - ID Chip 1 - Insert 1 - Detector tube (Granule) 25 - Detector diluent (5.5 mL) 1