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 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.
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 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%.
Product Details: Brand J.Mithra Result Time (Rapid Kits) Within 20 Minutes Test Kit Type Malaria Test Kit (Rapid) Sensitivity & Specificity Excellent as per WHO Malaria RDTs Evaluation Cat. No IR221050 Intended Use:Advantage MAL Card is a visual, rapid and sensitive immunoassay for the qualitative diagnosis of P.falciparum and other Plasmodium Species (P.vivax/ P.malariae/ P.ovale/ P.falciparum) based on pLDH antigen in human whole blood. Salient Features: Infection free- See through Device based on pLDH antigen Malaria parasite in whole blood Excellent Sensitivity & Specificity as per WHO Malaria RDTs Evaluation. Longer shelf life of 30 months at 4-30 C. Easy to interpret Colour Bands Results within 20 minutes.
Product Details: Brand J.Mithra Result Time (Rapid Kits) Within 3 Minutes Test Kit Type HCV Test Kit (Rapid) Sensitivity 100% WHO Evaluation Specificity 98.9% WHO Evaluation Cat. No HC020100 Intended Use: The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of (IgM,IgG & IgA) antibodies to Hepatitis C virus in human serum or plasma. It has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigen Salient Features: Based on Flow Through Technology, which is similar to Elisa technology because of involvement of washing steps at various levels to enhance the specificity. Use of highly purified HCV antigens for Core, NS3, NS4, NS5 immobilized on the device. Detection of all the subtypes of HCV. Results within 3 minutes. In built quality control dot which validates the test. 100% Sensitivity & 98.9% Specificity as per WHO evaluation. Shelf life : 24 months at 2-8C
Product Details: Brand Abbott Afinion Result Time (Rapid Kits) 15 min Sample Type Blood Country of Origin Made in India Requires only 20 ml of specimen Capillary tubes 20 ml Immediate point of care HbA1c results for efficient monitoring of glycemic control. The Afinion HbA1c assay is a test for quantitative determination of glycated hemoglobin (HbA1c) in human whole blood, used to monitor metabolic control in patients with diabetes. It provides the immediate test results you need for improved diabetic control, better patient outcomes, and enhanced clinic efficiencies. SHORT ASSAY TIME IN 3 MINUTES The CLIA-Waived Afinion HbA1c test gives you reliable, high quality results conveniently available when and where you need them. TIMELY TREATMENT CHANGES Diabetes can be treated and managed by healthful eating, regular physical activity, and medications to lower blood glucose levels. Lowering the HbA1c has been shown to reduce microvascular complications of diabetes and is also associated with long-term reduction in macrovascular disease. LONG SHELF LIFE OF REAGENTS Patient consultations can be carried out with confidence. The HbA1c Test Cartridge contains all reagents necessary for the measurement of glycated hemoglobin. The test has 3 months room temperature storage.
Product Details: Material Hips Usage/Application Clinical Country of Origin Made in India Sample Volume 2.5 microlitre Brand Abbott model number AFINION CRP Assay time 3 to 4 minutes Sample material Capillary blood,serum,plasma,or anticoagulated venous blood (EDTA or heparin) Measuring range 5-200 mg/L (whole blood),5-160 mg/L (serum and plasma Abbott AFINION CRP Rapid Vitro Diagnostic Test
Product Details: Usage/Application Hospital Country of Origin Made in India The Afinion Lipid Panel test and the fully automated Afinion Analyzer, give you reliable results conveniently available when and where you need them. Patient consultations can be carried out with confidence. Test for quantitative determination of Total Cholesterol, High-Density Lipoprotein (HDL) cholesterol, Low- Density Lipoprotein (LDL) cholesterol, Triglycerides (Trig), non-HDL and Chol/HDL ratio in whole blood, serum and plasma to be used in the diagnosis and treatment of lipid disorders. BENEFITS: Test for the quantitative determination of: THE IMPORTANCE OF MEASURING A LIPID PANEL Elevated cholesterol is one of the major risk factors for coronary heart disease, heart attack and stroke. As the blood cholesterol rises, so does the cardiovascular disease risk. Many patients such as those with metabolic syndrome have comorbid conditions such as high lipids and diabetes. And if other risk factors are present such as smoking, high blood pressure or diabetes, the risk increases even further. Measuring a Lipid Panel/Cholesterol is recommended by NCEP (National Cholesterol Education Program) every five years in healthy adults, more regularly if you have other risk factors, in children and youths who are at an increased risk and to evaluate the success of lipid-lowering treatment. See how POC diabetes testing significantly impacts patient care with better glycemic control, increased compliance, and improved office efficiencies. Read the presentation or download the PowerPoint for your own use.
Product Details: Number of Reactions(Preps)/Kit : 100 Brand : Siemens The Multistix 10 SG reagent strip is the reliable frontline test for detection of a broad range of conditions, from detecting urinary tract infections (UTI1) to diabetes and kidney disorders. Accurately gain a broader clinical insight into a patient's health.
Product Details: Number of Reactions(Preps)/Kit : 96 wells Brand : Abbott Usage/Application : Hospital Sample Material : Serum CAT No : 11EK10 The Panbio Dengue IgM Capture ELISA is used to detect IgM antibodies to dengue antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Panbio. Dengue IgM Capture ELISA should be used in conjunction with other dengue serology.
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 : 96 Wells Brand : InBios Sample Material : Serum Incubation Time: 60+60+60+5+10+1 Storage 2-8 C Cat No : DDMS-1 The DENV DetectTM IgM Capture ELISA is for the qualitative detection of IgM antibodies to DENV recombinant antigens in serum for the presumptive clinical laboratory diagnosis of Dengue virus infection. The assay is intended for use only in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever. The complete kit includes one 96 well strippable plate with all necessary reagents and controls. 1st Assay to Receive FDA Clearance. Performance thoroughly evaluated with clinically confirmed cases of dengue 1-4 serotypes. Excellent positive and negative agreement with WHO reference panel (>90%). Improves accuracy by monitoring background reactivity with a normal cell antigen. Employs a simple, one step ratio method of interpretation. CE Marked.
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 Cat. No : 01PE40 Panbio Dengue Early ELISA is a dengue NS1 antigen capture ELISA. It is used to detect NS1 antigen in serum as an aid to clinical laboratory diagnosis of patients with clinical symptoms consistent with dengue fever. The Dengue Early ELISA should be used in conjunction with other dengue serological assays.
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : CTK BioTech Sample : Serum / Plasma Storage : 2-8 C Cat No : AE0315 The TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay for the qualitative detection of IgM anti- Chikungunya virus in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with Chikungunya viruses. Any reactive specimen with the TRUSTwell CHIK IgM Test must be confirmed with alternative testing method(s) and clinical findings. TEST PRINCIPLE: TRUSTwell CHIK IgM Test is a solid phase enzyme linked immunoabsorbent assay based on the principle of the indirect immunoassay technique for the detection of IgM anti- Chikungunya virus in human serum or plasma. The TRUSTwell CHIK IgM Test is composed of two key components: 1) Solid microwells pre-coated with recombinant CHIK antigen(s); 2) Liquid conjugates composed of monoclonal anti-human IgM reagent conjugated with horse reddish peroxidase (HRP-anti-Human IgM conjugates). During the assay, the test specimen is first incubated with the coated microwells. IgM anti- Chikungunya virus, if present in the specimen, binds to the antigen coated on the microwell surface. In the second incubation with the HRP-anti Human IgM conjugates, the IgM antiChikungunya antibody absorbed on the surface of microwell reacts to the conjugates, forming a complexed 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 336 specimens from susceptible subjects were tested by TRUSTwell CHIK IgM and by a commercial reference ELISA kits. Relative Sensitivity: 91.3 %, (95 % CI: 73.2 % -97.6 %) Relative Specificity: 96.8 %, (95 % CI: 94.2 % -98.3 %) Overall Agreement: 96.4%, (95 % CI: 93.9 % -98.0 %).
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : CTK BioTech Sample : serum / plasma Storage : 2 - 8 C Cat No : AE0710 INTENDED USE: The TRUSTwell HBsAg ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of hepatitis B virus surface antigen (HBsAg) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HBV. Any reactive specimen with the TRUSTwell HBsAg ELISA Kit must be confirmed with alternative testing method(s) and clinical findings. TEST PRINCIPLE: TRUSTwell HBsAg ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of antibody sandwich technique for the detection of HBsAg in human serum or plasma. The TRUSTwell HBsAg ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with monoclonal anti HBsAg antibody; 2) Liquid conjugates composed of polyclonal anti-HBsAg conjugated with horse radish peroxidase (HRP-HBsAb conjugates). During the assay, the test specimen and HRP-HBsAb conjugates are incubated simultaneously with the coated microwells. HBsAg, if present in the specimen, reacts to the anti-HBsAg antibody coated on the microwell surface as well as the HRPHBsAb conjugate, 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 absorbance are read using a spectrophotometer at 450 /620-690 nm. Clinical Performance: A total of 1033 patient specimens from susceptible subjects were tested by the TRUSTwell HBsAg ELISA Kit. Relative Sensitivity:100%, Relative Specificity:99.78%, Overall Agreement:99.81%
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : CTK BioTech Sample : serum / plasma Storage : 2-8 C Cat No : AE0420 INTENDED USE: The TRUSTwell HIV Ag-Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of HIV-1 P24 antigen, anti-HIV-1 including subtype O and anti-HIV-2 antibodies (including isotype IgG, IgM and IgA) in human serum or plasma. It is intended for professional use only as an aid in the early identification of infection with HIV-1 and HIV-2 viruses. Any reactive specimen with the TRUSTwell HIV Ag-Ab ELISA Kit must be confirmed with alternative testing method(s) and clinical findings. TEST PRINCIPLE: The TRUSTwell HIV Ag-Ab ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the double antibody/antigen sandwich technique for the detection of HIV-1 P24 antigen and various antibodies against HIV-1 and/or HIV-2 antigen in human serum or plasma. The TRUSTwell HIV Ag-Ab ELISA Kit is composed by two systems: 1) Solid microwells pre-coated with Recombinant HIV-1 and HIV-2 antigens and anti-P24 antibody 2) Liquid conjugates composed of a. Recombinant HIV-1 and HIV-2 antigens conjugated with horse radish peroxidase (HRP-HIV 1+2 conjugates) and avidin conjugated with HRP (HRP-avidin conjugates) b. Anti-P24 antibody conjugated with biotin (Biotinylated P24 Ab) During the assay, the test specimen is first incubated with the coated microwells and followed by incubation with biotinylated P24 Ab. The anti-HIV-1 and anti-HIV-2 antibodies, if present in the specimen, bind to the antigens coated on the microwell surface. If P24 present in the specimen, binds to the anti-P24 antibody on the microwell surface and biotinylated P24 Ab in the solution. In the next incubation with the HRP-HIV 1+2 and HRP-avidin conjugates, the above bounded anti-HIV-1 and anti-HIV-2 antibodies and bounded P24 antigen reactive to the HRP conjugates, forming HRP-complex. 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 absorbance are read using a spectrophotometer at 450/620-690nm. Clinical Performance: A total of 1100 patient specimens from susceptible subjects were tested by the TRUSTwell HIV Ag-Ab ELISA Kit. Relative Sensitivity: 100%, Relative Specificity: 99.9%, Overall Agreement: 99.9%.
