Products We Offer
- Advantage Chikungunya Igm Card
- Diagnos HCV Bi-Dot
- Vitamin D Quanti Microlisa
- Vitamin B12 Quanti Microlisa
- TSH Quanti Microlisa
- T4 Quanti Microlisa
- T3 Quanti Microlisa
- Chikungunya IgM Microlisa
- 4th Generation Microlisa HIV Ag & Ab
- Dengue IgM Microlisa
- Dengue IgG Microlisa
- HCV Tri-Dot
- Celiac Microlisa
- Hepalisa Ultra
- Advantage Mal Card
- Hepacard Test Kit
- Dengue Ns1 Antigen FP
- HIV Tri-Dot Plus Ag
- Advantage P.f Malaria Card
- Advantage Malaria Card
- Advantage Malaria Pan Plus Pf Card
- Advantage Pan Malaria Card
- Diagnos Dengue Card
- Advantage Leptospira IgM & IgG Card
- Advantage Dengue NS1 Ag Card
- Diagnos HIV Bi-Dot
- Dengue NS1 Ag Microlisa
- Hepalisa Test Kit
- HIV Tri-Dot
- Dengue Day 1 Test
- Microlisa HIV
- Advantage Typhi Igm & Igg Card
- Lepto IgM Microlisa
- Dengue Ns1 Card Test
Diagnostics Solutions

Advantage Chikungunya Igm Card
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Results Time | 15 minutes |
Shelf Life | 24 months |
Packaging Size | 10,25,30 Tests |
Packaging Type | Paper Box |
Advantage Chikungunya IgM Card is a one step Immunochromatographic assay based on sandwich principle. The test sample is introduced which flows laterally through an absorbent pad where it mixes with the conjugate. If the sample contains Chikungunya specific IgM antibodies, it forms a complex with the conjugate. The complex then migrates through the nitrocellulose membrane by capillary action. When the complex meets the line of immobilized capture reagents (Test Line ’T’), it generates a pink purple line, indicating that the sample is reactive .To serve as a procedural control, an additional control line ‘C’ has been immobilized at a distance from the test line on the strip. If the test is performed correctly, this will result in the formation of a pinkish-purple line at the control region upon contact with the conjugate.
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Diagnos HCV Bi-Dot
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10-50 Test |
Result Time | 3 min |
Sensitivity | 100 % |
Shelf Life | 15 months |
Packaging Type | Paper Box |
Use of | Unique Combination of Core, NS3, NS4, NS5 antigen |
Specificity | 99.8 % |
The 4th Generation DIAGNOS HCV BI-DOT is a visual, rapid, sensitive and qualitative in vitro diagnostic test for the detection of antibodies to Hepatitis C Virus in human serum or plasma. The 4th Generation DIAGNOS HCV BI-DOT has been developed and designed with increased sensitivity for core and NS3 antibodies using a unique combination of modified HCV antigens.
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 12 Months |
Packaging Type | Paper Box |
Linearity Range | 2.70-130 ng/ml |
Analytical Sensitivity | 2.70 ng/ml |
Assay Procedure | 180 mins |
Vitamin D Quanti Microlisa is an enzyme immuno assay based on delayed competitive ELISA. First samples are incubated with assay diluent to release vitamin-D from binding protein in the sample. Vitamin D biotin conjugte is added in the microwells.
During incubation endogenous 25-OH vitamin D of a sample competes with a 25-OH vitamin D3-biotin conjugate for binding of the anti-vitamin D antibodies immobilized on the plate (this delayed competition increases the sensitivity for low concentration vitamin-D samples). Incubation is followed by a washing step to remove unbound components. During a second incubation, binding of 25-OH vitamin D-Biotin is detected by enzyme conjugate (peroxidase labelled streptavidin). Washing is followed.In the third incubation color reaction is started by addition of substrate and stopped after a defined time. The color intensity is inversely proportional to the concentration of 25-OH vitamin D in the sample.
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Vitamin B12 Quanti Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48 Tests |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Linearity Range | 50-2000 pg/ml |
Analytical Sensitivity | 50 pg/ml |
Assay Procedure | 170 mins |
Vitamin B12 Quanti Microlisa is an enzyme immuno assay based on competitive ELISA. First samples have to be pre-treated and separate in glass test tubes with working denaturation reagent to extract the vitamin B12 as circulating B12 is bound to binding protein in-vivo. After denaturation and neutralization, treated sample is added in the microwells. During incubation, endgenous vitamin B12 of a sample competes with the vitamin B12 biotinylated conjugate for binding of anti-vitamin B12 antibodies which is immobilized on the plate (this delayed competition increases the sensitivity for low concentration Vitamin B12 samples). Incubation is followed by a washing step to remove unbound components. During a second incubation, binding of Vitamin B12-Biotin is detected by enzyme conjugate (peroxidase labelled streptavidin). Washing is followed. In the third incubation color reaction is star ted by addition of substrate and stopped after a defined time. The color intensity is inversely proportional to the concentration of Vitamin B12 in the sample.
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TSH Quanti Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Linearity Range | 0.03 uIU/ml to 40 uIU/ml |
Assay Procedure | 75 mins |
Analytical Sensitivity | 0.03 uIU/ml |
TSH Quanti Microlisa is an enzyme immuno assay based on sandwich ELISA.Microwells are coated with anti-TSH antibodies. Sample is added to the microwell followed by addition of enzyme conjugate (anti-TSH labelled with HRP). Binding of TSH is detected by enzyme conjugate. Incubation is followed by a washing step to remove unbound components. The color reaction is started by addition of substrate and stopped after a defined time. The color intensity is directly proportional to the concentration of TSH in the sample.
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T4 Quanti Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Analytical Sensitivity | 0.4 ug/dl |
Assay Procedure | 75 mins |
Linearity Range | 0.4 ug/dl to 25 ug/dl |
T4 Quanti Microlisa is an enzyme immuno assay based on competitive ELISA.Microwells are coated with anti-thyroxine antibodies. Sample is added to the microwell followed by addition of enzyme conjugate (T4 labelled with HRPO). Binding of T4 is detected by Enzyme Conjugate. Incubation is followed by a washing step to remove unbound components. The color reaction is started by addition of substrate and stopped after a defined time. The color intensity is inversally proportional to the concentration of T4 in the sample.
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T3 Quanti Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 18 Months |
Sensitivity | 1.0 ng/mL |
Packaging Type | Paper Box |
Linearity Range | 0.1 ng/ml to 7.5 ng/ml |
Assay Procedure | 75 mins |
T3 Quanti Microlisa is an enzyme immuno assay based on competitive ELISA.Microwells are coated with anti-triiodothyronin antibodies. Sample is added to the microwell followed by addition of enzyme conjugate (T3 labelled with HRPO). Binding of T3 is detected by Enzyme Conjugate. Incubation is followed by a washing step to remove unbound components. The color reaction is started by addition of substrate and stopped after a defined time. The color intensity is inversally proportional to the concentration of T3 in the sample.
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Chikungunya IgM Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48 Tests |
Specificity | 99.93% |
Shelf Life | 24 Months |
Sensitivity | 99.35% |
Packaging Type | Paper Box |
Assay Procedure | 105 mins |
Chikungunya IgM Microlisa is designed for in vitro qualitative detection of Chikungunya IgM in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for Chikungunya.
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4th Generation Microlisa HIV Ag & Ab
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 12 Months |
Sensitivity | 100% |
Packaging Type | Paper Box |
Assay Procedure | 120 mins |
4TH GENERATION MICROLISA HIV Ag & Ab test is an enzyme immunoassay based on "Sandwich ELISA". HIV envelop proteins gp41 representing immunodominant epitopes and anti-p24 antibodies are coated into microtiter wells. Specimens and controls are added to the microtiter wells and incubated. Antibodies to HIV-1 and HIV-2 if present in the specimen, will bind to the specific antigens absorbed onto the surface of the wells. The plate is then washed to remove unbound material. Horseradish peroxidase (HRPO) conjugated gp41, C-terminus of gp120 of HIV-1 and gp36 of HIV-2 and anti-p24 antibodies is added to each well. The conjugate will bind to HIV antigen-antibody or anti-p24 antibody-antigen complex present. Finally substrate solution containing chromogen and hydrogen peroxide is added to the wells and incubated. A blue colour will develop in proportion to the amount of HIV-1 and/or HIV-2 antibodies and /or HIV-1 p24 antigen present in the specimen. The colour reaction is stopped by a stop solution. The enzyme substrate reaction is read by EIA reader for absorbance at a wavelength of 450 nm. If the sample does not contain HIV-1 or HIV-2 antibodies or HIV-1 p24 antigen, then enzyme conjugate will not bind and the solution in the wells will be either colourless or only a faint background colors develops.
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Dengue IgM Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48-96 Tests |
Specificity | 99.84% |
Shelf Life | 18 Months |
Sensitivity | 99.13% |
Packaging Type | Paper Box |
Dengue IgM Microlisa test is an enzyme immunoassay based on "CAPTURE ELISA". Anti-human IgM antibodies are coated onto microtiter wells. Specimens and controls are added to the microtiter wells and incubated. Antibodies to Dengue if present in the specimen, will bind to the anti- human IgM antibodies adsorbed onto the surface of the wells. The plate is then washed to remove unbound material. Horseradish peroxidase (HRPO) conjugated Dengue antigen (DEN-4) is added to each well. This dengue antigen conjugate will bind to dengue specific IgM antibodies which is complex with anti-human IgM antibodies. Finally substrate solution containing chromogen and hydrogen peroxide is added to the wells and incubated. A blue colour will develop in proportion to the amount of dengue antibodies present in the specimen. The colour reaction is stopped by a stop solution. The enzyme substrate reaction is ready by EIA reader for absorbance at a wavelength of 450 nm. If the sample does not contain dengue IgM antibodies then enzyme conjugate will not bind and the solution in the wells will be either colourless or only a faint background colour develops.
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Dengue IgG Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48-96 Tests |
Specificity | 99.93% |
Sensitivity | 96.00% |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Dengue IgG Microlisa is designed for in-vitro qualitative detection of Dengue IgG antibodies in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for DENGUE. The kit detects all four subtypes; DEN1, DEN2, DEN3 & DEN4 of Dengue Virus.
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HCV Tri-Dot
Rs 1 / UnitGet Latest Price
Method | Rapid |
Packaging Size | 50-100 Tests |
Sensitivity | 98.9% |
Shelf Life | 15 months |
Packaging Type | Paper Box |
Results Within | 3 minutes |
Use of Highly Purified | HCV antigens for Core,NS3,NS4,NS5 immobilized on the device |
The 4th Generation HCV TRI-DOT is a rapid, visual, sensitive and qualitative in vitro diagnostic test for the detection of 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.
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Celiac Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Specificity | 100% |
Shelf Life | 12 Months |
Packaging Type | Paper Box |
Excellent Sensitivity | 100% |
Celiac Microlisa is an in-vitro qualitative enzyme immunoassay for the detection of anti tTG IgA antibodies in Human Serum or Plasma. The assay is intended to be used as an aid in the recognition and diagnosis of Celiac disease.
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Hepalisa Ultra
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Shelf Life | 12 Months |
Packaging Type | Paper Box |
Antigen Sensitivity | 0.05 ng/ml |
4TH Generation Hepalisa Ultra is a solid phase enzyme linked immunosorbent assay (Elisa) based on the “Direct sandwich” principle. The microwells are coated with Monoclonal antibodies with high reactivity for HBsAg. The samples are added in the wells followed by addition of enzyme conjugate (polyclonal antibodies linked to Horseradish Peroxidase (HRPO)). A sandwich complex is formed in the well wherein HBsAg (from serum sample) is ‘’trapped’’ or ‘’sandwiched’’ between the antibody and antibody HRPO conjugate. Unbound conjugate is then washed off with wash buffer. The amount of bound peroxidase is proportional to the concentration of HBsAg present in the sample. Upon addition of the substrate buffer and chromogen, a blue colour develops. The intensity of developed blue colour is proportional to the concentration of the HBsAg in the sample. To limit the enzyme-substrate reaction, stop solution is added and a yellow colour develops which is finally read at 450 nm spectrophotometrically.
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Advantage Mal Card
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25 Tests |
Result Time | 20 minutes |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
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.
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Hepacard Test Kit
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 20,100,200 Tests |
Shelf Life | 24 Months |
Sensitivity | 100% |
Antigen Sensitivity | 0.5 ng/ml |
HEPACARD is visual, rapid, sensitive and accurate one step immunoassay for the qualitative detection of Hepatitis B surface antigen (HBsAg) in Human serum or plasma.The assay is intended to be used as an aid in the recognition and diagnosis of acute infections and chronic infectious carriers of the Hepatitis B Virus(HBV).
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Dengue Ns1 Antigen FP
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10-50 Tests |
Sensitivity | 100% |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Dengue NS1 Antigen FP is an immunoassay based on the "sandwich" principle. Dengue NS1 antigen device contains two lines; "C" (Control Line) & "T" (Dengue NS1 Antigen detection Test Line). Test line is coated with anti-dengue NS1 antibodies. When a sample is added to the device, Dengue NS1 antigen if present in the sample will bind to the anti-dengue NS1 gold colloid conjugate making antigen antibodies complex. On addition of assay buffer, this complex migrates along the membrane to the test region and forms the visible pink line at "T" as antibody-antigen-antibody gold conjugate complex.
The intensity of the test band in the device will vary depending upon the amount of antigen present in the sample. The appearance of any pink/red colour in test region should be considered as reactive for Dengue NS1 antigen. A red procedural control line should always develop in the test device window to indicate that the test has been performed properly.
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HIV Tri-Dot Plus Ag
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10-50 Tests |
Sensitivity | 100 % |
Packaging Type | Paper Box |
Use of | gp-41,C terminus of gp120 for HIV-1 antibodies & gp-36 for HIV -2 antibodies |
Detection of Group | 0 & subtype C of HIV-1 |
The 4th Generation HIV TRI-DOT + Ag test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 p24 antigen and HIV-1 & HIV-2 antibodies (IgG) in Human Serum or Plasma. The test is a screening test for p24 antigen (HIV-1), anti-HIV-1 & anti-HIV-2 and is for in vitro diagnostic use only. It is intended for screening of blood donors or other individuals at risk for HIV-1 & HIV-2 infection and for clinical diagnostic testing.
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Advantage P.f Malaria Card
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25 Tests |
Result Time | 20 minutes |
Sensitivity | 50 -100% |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Advantage P.f Malaria Card is an immunoassay based on the "Sandwich principle" . Colloidal gold is conjugated to monoclonal anti- Pf specific HRP-2 antibody. The test uses monoclonal anti-Pf HRP-2 antibody (test line F) immobilized on a nitrocellulose strip. The test sample is added to the device. On addition of assay buffer, the red blood cells get lysed.If the sample contains P.falciparum the colloidal gold conjugate complexes the Pf specific HRP-2 in the lysed sample. This complex migrates through the nitrocellulose strip by capillary action. When the complex meets the line of the corresponding immobilized antibody, the complex is trapped forming a purplish pink band which confirms a reactive test result. Absence of a coloured band in the test region indicates a negative test result. To serve as a procedural control an additional line of anti-mouse antibody has been immobilized on the strip as control.
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Advantage Malaria Card
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25 Tests |
Result Time | 20 minutes |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Advantage Malaria Card is a visual, rapid and sensitive immunoassay for the qualitative differential detection of P.falciparum (HRP-2) and P.vivax (pLDH) malaria antigen in human blood only.
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Advantage Malaria Pan Plus Pf Card
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25-50 Tests |
Result Time | 20 minutes |
Sensitivity | 100% |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Advantage Malaria Pan Plus Pf Card is an immunoassay based on the "Sandwich” principle. The conjugate contains colloidal gold conjugated to Pf specific monoclonal anti- HRP-2 antibody and monoclonal anti-pan specific pLDH antibody. The test uses monoclonal anti-Pf HRP-2 antibody (test line F) & monoclonal anti-pan specific pLDH antibody (test line P) immobilized on a nitrocellulose strip. The test sample is added to the device. On addition of assay buffer, the red blood cells get lysed. If the sample contains P.falciparum or P.vivax/P.malariae/P.ovale, the colloidal gold conjugate complexes the Pf specific HRP-2/ Pan specific pLDH in the lysed sample. This complex migrates through the nitrocellulose strip by capillary action. When the complex meets the line of the corresponding immobilized antibody, the complex is trapped forming a purplish pink band which confirms a reactive test result. Absence of a coloured band in the test region indicates a negative test result. To serve as a procedural control an additional line of anti-mouse antibody has been immobilized on the strip as control.
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Advantage Pan Malaria Card
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25 Tests |
Result Time | 20 minutes |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Advantage Pan Malaria Card is a rapid, visual and sensitive immunoassay for the qualitative diagnosis of all four Plasmodium Species (P.falciparum/P.vivax/P.malariae/P.ovale) based on pLDH antigen in human whole blood only.
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Diagnos Dengue Card
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10 Tests |
Result Time | 20 minutes |
Sensitivity | 91% |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Diagnos Dengue card test is based on immunochromatographic test principle for the differential detection of Dengue IgM/IgG antibodies.
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 red particles coated with Dengue proteins. As this sample/particle mixture migrates along the length of the test, the anti-dengue IgG or IgM antibody particle complex is captured by the relevant IgG and /or IgM test bands located in the test device 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 device will vary depending upon the amount of antigen /antibody present in the sample. The appreance 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.
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Advantage Leptospira IgM & IgG Card
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Sensitivity | 99 % |
Specificity | 99.5% |
Test Results | 20 minutes |
Shelf Life | 18 months |
Pack Size | 10 Tests |
Pack Type | Paper Box |
Application | Hospital |
Advantage Leptospira IgM & IgG card test is based on Immunochromatographic assay principle. The test sample is introduced to and flows laterally through an absorbent pad where it mixes with the conjugate. If the sample contains Leptospira specific IgM and/or IgG antibodies, it forms a complex with the conjugate. The complex then migrates through the nitrocellulose membrane by capillary action. When the complex meets the immobilized antibodies (Test line ‘M & G’), it generates a red line, indicating that the sample is reactive. To serve as a procedural control, an additional control line ‘C’ has been immobilized at a distance from the test line on the strip. If the test is performed correctly, this will result in the formation of a red line at the control region upon contact with the conjugate.
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Advantage Dengue NS1 Ag Card
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 25 Tests |
Result Time | 20 minutes |
Sensitivity | 93% |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Advantage Dengue NS1 Ag card test is based on immunochromatographic test principle for the detection of Dengue NS1 antigen. 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 “T” as antibody-antigen-antibody gold colloid forms.
The intensity of the test bands in the device will vary depending upon the amount of antigen present in the sample. The appreance of any pink. red colour in a specific test region should be considered as positive for that particular antigen. A red procedural control line should always develop in the test device window to indicate that the test has been performed properly.
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Diagnos HIV Bi-Dot
Rs 1 / UnitGet Latest Price
Method | Rapid |
Packaging Size | 50-100 Test |
Shelf Life | 15 months |
Packaging Type | Paper Box |
Detection of Group | O & subtype C strain of HIV-1 |
Use of Envelope Antigen | gp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2 |
Results Within | 3 minutes |
The DIAGNOS HIV BI-DOT Test is a visual, rapid, sensitive and accurate immunoassay for the detection of HIV-1 & HIV-2 antibodies (IgG) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane.The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
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Dengue NS1 Ag Microlisa
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48-96 Tests |
Sensitivity | 99.50% |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Specificity | 100% |
Dengue NS1 Ag Microlisa is a solid phase enzyme linked immunosorbent assay (ELISA) based on the "Direct Sandwich" principle. The microwells are coated with Anti-Dengue NS1 antibodies with high reactivity for Dengue NS1 antigen. The samples are added in the wells followed by addition of enzyme conjugate (monoclonal anti-dengue NS1 antibodies linked to Horseradish peroxidase (HPRO)). A sandwich complex is formed in the well wherein dengue NS1 (from serum sample) is ‘’trapped’’ or ‘’sandwiched’’ between the antibody and antibody HRPO conjugate. Unbound conjugate is then washed off with wash buffer. The amount of bound peroxidase is proportional to the concentration of dengue NS1 antigen present in the sample. Upon addition of the substrate buffer and chromogen, a blue colour develops. The intensity of developed blue colour is proportional to the concentration of dengue NS1 antigen in sample. To limit the enzyme-substrate reaction, stop solution is added and a yellow colour develops which is finally read at 450 nm spectrophotometrically.
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Hepalisa Test Kit
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Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Result Time | 96 Tests |
Shelf Life | 15 months |
Packaging Type | Paper Box |
Assay Procedure | 90 mins |
Antigen Sensitivity | 0.1 ng/ml |
HEPALISA is a solid phase enzyme linked immunosorbent assay based on the Direct Sandwich Elisa principle. The microwells are coated with Monoclonal antibodies with high reactivity for HBsAg. The samples are added in the wells followed by addition of enzyme conjugate (polyclonal antibodies linked to Horseradish Peroxidase (HRPO). A sandwich complex is formed in the well wherein HBsAg (from serum sample) is "trapped" or "sandwiched" between the antibody and antibody HRPO conjugate. Unbound conjugate is then washed off with wash buffer. The amount of bound peroxidase is proportional to the concentration of HBsAg present in the sample. Upon addition of the substrate buffer and chromogen, a blue colour develops. The intensity of developed blue colour is proportional to the concentration of HBsAg in sample. To limit the enzyme-substrate reaction, stop solution is added and a yellow colour develops which is finally read at 450 nm spectrophotometrically.
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HIV Tri-Dot
Rs 1 / UnitGet Latest Price
Packaging Size | 10 Tests,50 Tests and 100 Tests |
Sensitivity | 100% |
Shelf Life | 15 months |
Differential Detection of | HIV-1 & HIV-2 |
Detection of Group | O & subtype C |
Results Within | 3 minutes |
The HIV TRI-DOT test is a visual, rapid, sensitive and accurate immunoassay for the differential detection of HIV-1 & HIV-2 antibodies (IgG) in human serum or plasma using HIV-1 & HIV-2 Antigens immobilized on an immunofiltration membrane. The test is a screening test for Anti HIV-1 and HIV-2 and is for in vitro diagnostic use only.
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Dengue Day 1 Test
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10, 30, 50 Tests |
Shelf Life | 24 Months |
Packaging Type | Paper Box |
Dengue Day 1 Test
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Microlisa HIV
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 96 Tests |
Sensitivity | 100 % |
Shelf Life | 15 months |
Packaging Type | Paper Box |
Assay Procedure | 90 mins |
Microlisa HIV test is an enzyme immunoassay based on Indirect Elisa. HIV envelop proteins gp-41, C terminus of gp-120 for HIV-1 and gp-36 for HIV-2 representing Immunodominant epitopes are coated onto microtiter wells. Specimens and controls are added to the microtiter wells and incubated. Antibodies to HIV-1 and HIV-2 if present in the specimen, will bind to the specific antigens adsorbed onto the surface of the wells. The plate is then washed to remove unbound material. Horseradish peroxidase (HRPO) conjugated anti-human IgG is added to each well. This conjugate will bind to HIV antigen-antibody complex present. Finally substrate solution containing chromogen and hydrogen peroxide is added to the wells and incubated. A blue colour will develop in proportion to the amount of HIV-1 and / or HIV-2 antibodies present in the specimen. The colour reaction is stopped by stop solution. The enzyme substrate reaction is read by EIA reader for absorbance at a wavelength of 450 nm. If the sample does not contain HIV-1 or HIV-2 antibodies then enzyme conjugate will not bind and the solution in the wells will be either colorless or only a faint background colour develops.
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Advantage Typhi Igm & Igg Card
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Usage/Application | Hospital |
Method | Rapid |
Packaging Size | 10-50 Tests |
Result Time | 20 minutes |
Shelf Life | 18 Months |
Packaging Type | Paper Box |
Advantage Typhi IgM & IgG Card is a lateral flow immunochromatographic assay. The test uses anti-human IgM antibody (test line M) and anti-human IgG (test line G) immobilised on a nitrocellulose strip. The conjugate contains colloidal gold conjugated to S. typhi antigen. When a specimen followed by assay buffer is added to the sample well S. Typhi specific IgM &/or IgG antibodies if present, will bind to S. Typhi antigen gold conjugate making antigen antibodies complex. This complex migrates through nitrocellulose membrane by capillary action. When the complex meets the line of the corresponding immobilized antibody (anti-human IgM &/or anit-human IgG) the complex is trapped forming a purplish pink band which confirm a reactive test result. Absence of a coloured band in the test region indicates a non reactive test result. A red procedural control line should always develop in the test device window to indicate that the test has been performed properly.
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Lepto IgM Microlisa
Rs 1 / UnitGet Latest Price
Usage/Application | Hospital |
Method | Elisa |
Packaging Size | 48 Tests |
Shelf Life | 12 Months |
Sensitivity | 99.62% |
Packaging Type | Paper Box |
Test Procedure | 90 mins |
Lepto IgM Microlisa is designed for in-vitro qualitative detection of Leptospira IgM in human serum or plasma and it is used as a screening test for testing of collected blood samples suspected for Leptospirosis.
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Dengue Ns1 Card Test
Rs 55 / PieceGet Latest Price
Brand | high quality |
high quality of dengue card
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