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 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: 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 : 50 Brand : SD ICMR Approved : Yes Result Time (Rapid Kits) : 15 min Sample Type : Oral & Nasal Swab STANDARD E Dengue IgM ELISA analyzes IgM antibodies specific to Dengue virus in serum and plasma using enzyme linked immunosorbent assay.
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : InBios Sample Material : Serum Format : Antigen Detection Incubation Time : 60+30+20+1 Cat No : DNS1-1 The DENV DetectTM NS1 ELISA is for the early detection of Dengue virus (DENV) NS1 antigen in human serum. This test is for the presumptive clinical laboratory diagnosis of Dengue virus infection. This assay is intended for use in patients with clinical symptoms consistent with either dengue fever or dengue hemorrhagic fever. Samples collected from patients within seven (7) days after the onset of clinical symptoms should be evaluated with this assay (day 0 â?? day 7). Negative results obtained with this test do not preclude the diagnosis of dengue and should not be used as the sole basis for treatment or other patient management decision. This assay is not FDA cleared or approved for testing blood or plasma donors. The complete kit includes one 96 well strippable plate with all necessary reagents and controls. FDA Cleared & CE Marked Early NS1 antigen detection (within first 7 days onset of symptoms) Helps differentiate dengue from other flaviviruses that may cross react with dengue antibodies but not with the antigen High Sensitivity & Specificity: 86.6% PPA & 97.8% NPA with prospectively collected positive and negative confirmed clinical specimens Kit can be performed in parallel with InBiosâ?? FDA Cleared dengue IgM ELISA for presumptive diagnosis of acute or convalescent stage dengue virus.
Product Details: Quantity/Kit : 96 wells/Plate Format :Indirect Brand : InBios Incubation Time : 30 + 30 +10 + 1 Sample Type : Serum or dried blood spots Cat No : FILA-1 he Filaria DetectTM IgG4 ELISA is for qualitative detection of specific IgG4 antibodies in specimens to highlyspecific antigen IWb123 target antigen expressed primarily in infective stage larvae (L3) of the lymphatic-dwelling parasite Wuchereria bancrofti (Wb). This product is for research use only. Not for use in diagnostic procedures. The complete kit includes one 96 well strippable plate with all necessary reagents and controls. For research purposes only.
Product Details: Number of Reactions(Preps)/Kit : 96 Wells Brand : InBios Sample Material : Serum Format : ELISA Incubation Time : 30 + 30 + 5 + 10 + 1 Cat No : STMS-R The Scrub Typhus Detect IgM ELISA for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA system for the detection of IgM antibodies in human serum to OT-derived recombinant antigen. This test is for research use only. Not for use in diagnostic procedures. The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Product Details: Size 96 wells/Plate Format Indirect Incubation Time 30 + 30 + 5 + 10 + 1 Sample Type Serum Storage 2-8 C Cat No STGS-R The Scrub Typhus Detectâ?¢ IgG ELISA test for exposure to Orientia tsutsugamushi (OT; formerly Rickettsia) is an ELISA assay system for the detection of IgG antibodies in human serum to OT-derived recombinant antigen. For research use only. Not for use in diagnostic procedures. The complete kit includes one 96 well strippable plate with all necessary reagents and controls.
Product Details: Number of Reactions(Preps)/Kit ; 96 Wells Brand : InBios Format : Immunocapture Specimen : Serum Cat No : ZKM2-1 The ZIKV Detect 2.0 IgM Capture ELISA is intended for the qualitative detection of Zika virus IgM antibodies in human sera for the presumptive clinical laboratory diagnosis of Zika virus infection. The assay is intended for use only in patients with clinical signs and symptoms consistent with Zika virus infection, and/or CDC Zika virus epidemiological criteria (e.g., history of residence in or travel to a geographic region with active Zika transmission at the time of travel, or other epidemiological criteria for which Zika virus testing may be indicated). Assay results are for the presumptive detection of IgM antibodies to Zika virus (ZIKV). Positive results must be confirmed by following the latest CDC guidelines for the diagnosis of Zika virus infection. Results of this test are intended to be used in conjunction with clinical observations, patient history, epidemiological information, and other laboratory evidence to make patient management decisions. Zika IgM levels are variable over the course of the infection and may be detectable near day four post onset of symptoms and persist up to approximately 12 weeks following initial infection. Negative results may be seen in specimens collected before day four post onset of symptoms or after the window of detectable IgM closes, and therefore do not preclude the possibility of Zika virus infection, past or present. 1st Commercial serology kit to receive FDA Marketing Authorization CE Marked Differentiates Zika IgM positive patients from those infected with other flaviviruses such as West Nile or Dengue Sensitivity: >90% Specificity: >96% Results in 4 hours Tests up to 28 unknown specimens.
