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Diagnostics Solutions

Our product range includes a wide range of Advantage Chikungunya Igm Card, Diagnos HCV Bi-Dot, Vitamin D Quanti Microlisa, Vitamin B12 Quanti Microlisa, TSH Quanti Microlisa and T4 Quanti Microlisa.

Advantage Chikungunya Igm Card
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Advantage Chikungunya Igm Card

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Usage/ApplicationHospital
Results Time15 minutes
Shelf Life24 months
Packaging Size10,25,30 Tests
Packaging TypePaper 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
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Diagnos HCV Bi-Dot

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Usage/ApplicationHospital
MethodRapid
Packaging Size10-50 Test
Result Time3 min
Sensitivity100 %
Shelf Life15 months
Packaging TypePaper Box
Use ofUnique Combination of Core, NS3, NS4, NS5 antigen
Specificity99.8 %

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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Vitamin D Quanti Microlisa
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Vitamin D Quanti Microlisa

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Minimum Order Quantity: 1 Piece

Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life12 Months
Packaging TypePaper Box
Linearity Range2.70-130 ng/ml
Analytical Sensitivity2.70 ng/ml
Assay Procedure180 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/ApplicationHospital
MethodElisa
Packaging Size48 Tests
Shelf Life18 Months
Packaging TypePaper Box
Linearity Range50-2000 pg/ml
Analytical Sensitivity50 pg/ml
Assay Procedure170 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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TSH Quanti Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life18 Months
Packaging TypePaper Box
Linearity Range0.03 uIU/ml to 40 uIU/ml
Assay Procedure75 mins
Analytical Sensitivity0.03 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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T4 Quanti Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life18 Months
Packaging TypePaper Box
Analytical Sensitivity0.4 ug/dl
Assay Procedure75 mins
Linearity Range0.4 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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T3 Quanti Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life18 Months
Sensitivity1.0 ng/mL
Packaging TypePaper Box
Linearity Range0.1 ng/ml to 7.5 ng/ml
Assay Procedure75 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/ApplicationHospital
MethodElisa
Packaging Size48 Tests
Specificity99.93%
Shelf Life24 Months
Sensitivity99.35%
Packaging TypePaper Box
Assay Procedure105 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/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life12 Months
Sensitivity100%
Packaging TypePaper Box
Assay Procedure120 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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Dengue IgM Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size48-96 Tests
Specificity99.84%
Shelf Life18 Months
Sensitivity99.13%
Packaging TypePaper 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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Dengue IgG Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size48-96 Tests
Specificity99.93%
Sensitivity96.00%
Shelf Life18 Months
Packaging TypePaper 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
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HCV Tri-Dot

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MethodRapid
Packaging Size50-100 Tests
Sensitivity98.9%
Shelf Life15 months
Packaging TypePaper Box
Results Within3 minutes
Use of Highly PurifiedHCV 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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Celiac Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Specificity100%
Shelf Life12 Months
Packaging TypePaper Box
Excellent Sensitivity100%

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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Hepalisa Ultra

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Shelf Life12 Months
Packaging TypePaper Box
Antigen Sensitivity0.05 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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Advantage Mal Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size25 Tests
Result Time20 minutes
Shelf Life24 Months
Packaging TypePaper 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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Hepacard Test Kit

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Usage/ApplicationHospital
MethodRapid
Packaging Size20,100,200 Tests
Shelf Life24 Months
Sensitivity100%
Antigen Sensitivity0.5 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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Dengue Ns1 Antigen FP

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Usage/ApplicationHospital
MethodRapid
Packaging Size10-50 Tests
Sensitivity100%
Shelf Life24 Months
Packaging TypePaper 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
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HIV Tri-Dot Plus Ag

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Usage/ApplicationHospital
MethodRapid
Packaging Size10-50 Tests
Sensitivity100 %
Packaging TypePaper Box
Use ofgp-41,C terminus of gp120 for HIV-1 antibodies & gp-36 for HIV -2 antibodies
Detection of Group0 & 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
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Advantage P.f Malaria Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size25 Tests
Result Time20 minutes
Sensitivity50 -100%
Shelf Life24 Months
Packaging TypePaper 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
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Advantage Malaria Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size25 Tests
Result Time20 minutes
Shelf Life24 Months
Packaging TypePaper 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
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Advantage Malaria Pan Plus Pf Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size25-50 Tests
Result Time20 minutes
Sensitivity100%
Shelf Life24 Months
Packaging TypePaper 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
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Advantage Pan Malaria Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size25 Tests
Result Time20 minutes
Shelf Life24 Months
Packaging TypePaper 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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Diagnos Dengue Card

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Usage/ApplicationHospital
MethodRapid
Packaging Size10 Tests
Result Time20 minutes
Sensitivity91%
Shelf Life24 Months
Packaging TypePaper 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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Sensitivity99 %
Specificity99.5%
Test Results20 minutes
Shelf Life18 months
Pack Size10 Tests
Pack TypePaper Box
ApplicationHospital

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/ApplicationHospital
MethodRapid
Packaging Size25 Tests
Result Time20 minutes
Sensitivity93%
Shelf Life24 Months
Packaging TypePaper 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
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Diagnos HIV Bi-Dot

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MethodRapid
Packaging Size50-100 Test
Shelf Life15 months
Packaging TypePaper Box
Detection of GroupO & subtype C strain of HIV-1
Use of Envelope Antigengp41& C terminus of gp120 for HIV-1 & gp36 for HIV-2
Results Within3 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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Dengue NS1 Ag Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size48-96 Tests
Sensitivity99.50%
Shelf Life18 Months
Packaging TypePaper Box
Specificity100%

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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Hepalisa Test Kit

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Result Time96 Tests
Shelf Life15 months
Packaging TypePaper Box
Assay Procedure90 mins
Antigen Sensitivity0.1 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
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HIV Tri-Dot

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Packaging Size10 Tests,50 Tests and 100 Tests
Sensitivity100%
Shelf Life15 months
Differential Detection ofHIV-1 & HIV-2
Detection of GroupO & subtype C
Results Within3 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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Dengue Day 1 Test

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Usage/ApplicationHospital
MethodRapid
Packaging Size10, 30, 50 Tests
Shelf Life24 Months
Packaging TypePaper Box

Dengue Day 1 Test

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Microlisa HIV
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Microlisa HIV

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Usage/ApplicationHospital
MethodElisa
Packaging Size96 Tests
Sensitivity100 %
Shelf Life15 months
Packaging TypePaper Box
Assay Procedure90 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/ApplicationHospital
MethodRapid
Packaging Size10-50 Tests
Result Time20 minutes
Shelf Life18 Months
Packaging TypePaper 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
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Lepto IgM Microlisa

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Usage/ApplicationHospital
MethodElisa
Packaging Size48 Tests
Shelf Life12 Months
Sensitivity99.62%
Packaging TypePaper Box
Test Procedure90 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

Brandhigh quality

high quality of dengue card 

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Matrics SolutionsC 122, Sector 10, www.matricssolution.com, http://matricssolution.com/, Noida, Gautam Budh Nagar-201301, Uttar Pradesh, India

T.K. Gupta (CEO)

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