Product Details:
Number of Reactions(Preps)/Kit 30T
Brand Abbott
Usage/Application Hospital
Result Time (Rapid Kits) 15 mins
Cat. No 02FK10I30
Bioline HCVHEPATITIS C VIRUS TEST
When speed matters, choosing a highly sensitive rapid HCV test with a safe fingerstick procedure can make a difference.
In the global effort to eliminating viral hepatitis, fast detection in a wide range of settings and linkage to care are critical for achieving successful outcomes
Bioline HCV test is a immunochromatographic rapid test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood.
Specification:
Specimen :
- Serum, Plasma, Whole Blood (10 �¼l) for 02FK10, 02FK10CE, 02FK16, 02FK16CE, 02FK17, 02FK17CE, 02FK11
- Serum or Plasma (10 l) for 02FK12
Sensitivity :
- 99.3% (95% CI: 97.9 - 99.8%) for 02FK10CE, 02FK16CE, 02FK17CE
- 99.3% (95% CI: 96.1 - 99.9%) for 02FK10, 02FK16, 02FK17
- 100 % (97.6 - 100 %) for 02FK11, 02FK12
Specificity :
- 100% (95% CI: 99.7 - 100 %) for 02FK10CE, 02FK16CE, 02FK17CE
- 98.1% (95% CI: 94.5 - 99.4%) for 02FK10, 02FK16, 02FK17
- 99.4 % (98.7 - 99.7 %) for 02FK11, 02FK12
Shelf life: 24 months at 1-30C
Qualitative immunochromatographic assay
Recombinant HCV core, NS3, NS4, NS5 Ag used as capture materials
Cat No.02FK10I30. SD BIOLINE HCV test is an immunochromatographic rapid visual test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood Immobilized material: Recombinant HCV Core, NS3, NS4, NS5 Ag Specimen Type: Serum, Plasma, Whole blood Sample Volume: 10MuL Shelf Life: 24months Storage: 2-30oC Performance: Sensitivity: 99.5% and Specificity: 98% One Step Hepatitis C Virus Test.
HCV Test Kit
HCV rapid diagnostics test kits(ce & iso)
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: Number of Reactions(Preps)/Kit 96 Wells Brand CTK BioTech Sample serum or plasma Storage 2 - 8 C Cat No : AE0510 INTENDED USE: The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of IgG to Hepatitis C virus (HCV) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with HCV. Any reactive specimen with the TRUSTwell HCV IgG ELISA Kit must be confirmed with alternative testing method(s) and clinical findings. TEST PRINCIPLE: The TRUSTwell HCV IgG ELISA Kit is a solid phase enzyme linked immunosorbent assay based on the principle of the indirect EIA technique for the detection of the IgG to HCV in human serum or plasma. The TRUSTwell HCV IgG ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with recombinant HCV antigens; 2) Liquid conjugates composed of mouse anti-human IgG conjugated with horse radish peroxidase (HRP-anti Human IgG conjugates). During the assay, the test specimen is first incubated with the coated microwells. The IgG anti HCV, if present in the specimen, bind to the antigens coated on the microwell surface. In the second incubation with the HRP-anti-human IgG conjugates, the IgG antibodies absorbed on the surface of microwell react to the HRP-anti-human IgG 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 1108 patient specimens from susceptible subjects were tested by the TRUSTwell HCV IgG ELISA Kit. Relative Sensitivity:100%, Relative Specificity:99.81%, Overall Agreement:99.82%.
Product Details: Usage/Application Hospital shelf life 18 months SD BIOLINE Syphilis 3.0 test is a solid phase immunochromatographic assay for the qualitative detection of antibodies of all isotypes (IgG, IgM, IgA) against Treponema pallidum (TP). Specimen: Serum, Plasma, Whole Blood Sample Volume: 10MuL Serum / Plasma and 20MuL Whole blood Recombinant TP, 15kDa, 17kDa antigens used as captures and detectors The optimal choice for mass screening program No need preprocessing and equipments Storage: Room temperature (2-30 degree C) Performance: Sensitivity: 99.3% Specificity: 99.5% One Step Syphilis Antibody Rapid test Ordering Information Cat No. Description Type Pack size 06FK10I50 SD Bioline Device 50 Tests Syphilis 3.0
Cat. No : 11FK45. SD BIOLINE Dengue Duo (Dengue NS1 Ag + IgG/IgM) The SD BIOLINE Dengue Duo kit is a rapid, an in-vitro immunochromatographic, one step assay designed to detect both dengue virus NS1 antigen and antibodies to Dengue virus (Dengue IgG/IgM) in human serum, plasma or whole blood. SD BIOLINE Dengue Duo rapid test contains two test devices (left side ; Dengue NS1 Ag test, right side ; Dengue IgG/IgM test). The SD BIOLINE Dengue Duo kit is intended only for an initial screening test and reactive samples should be confirmed by a supplemental assay such as RT-PCR, IgM / IgG ELISA or HI (Hemagglutination inhibition) test. Detect Dengue Ag and Ab simultaneously at once. Cover acute to convalescence stage Performance: Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM) Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM) In primary infection with the dengue virus, IgG antibody appears a few days after IgM. In primary infections, IgG antibodies are produced at a lower level compared to IgM but will persist for many years after infection. In secondary infections, IgG response may rise quickly before or simultaneously with an IgM response and will become the predominant immunoglobulin isotype in secondary infections.
Cat No. 08FK50. SD BIOLINE TB Ag MPT64 Rapid is a rapid immune chromatographic identification test for the M. tuberculosis complex. M. tuberculosis has been known to secrete more than 33 different proteins. One of the predominant proteins, MPT64 was found in the culture fluid of only strains of the M. tuberculosis complex. Rapid discrimination between the M. tuberculosis complex and MOTT bacilli Identification of the M. tuberculosis complex in combination with culture systems Sample: Colony, Condensation fluid(Solid cultures) or Liquid cultures Interpretation time: 15minutes Detection limit: 105CFU/ml.
Product Details: Number of Reactions(Preps)/Kit 30T Brand Abbott ICMR Approved Yes Result Time (Rapid Kits) 20Min Self Time 24 months Cat. No 03FK10CE Bioline HIV 1/2 3.0HIV 1/2 ANTIBODY TEST Bioline HIV 1/2 3.0 test is an immunochromatographic assay for the differential and qualitative detection of all isotypes (IgG, IgM, IgA) antibodies specific to HIV-1 including subtype O and HIV-2 simultaneously, in human serum, plasma or whole blood. Benefits: Highly sensitive even to IgM during early infection stage Differentiated test result between HIV type I and II by clear band formation (3-lines) Specimen : Serum, Plasma (10l), or Whole blood (20 l) 24 months at 1-30 Specification: Sensitivity : 100% Specificity : 99.8%