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Jun-24-22
 
Cat No : 05FK80I40. The SD BIOLINE Malaria Ag P.f/Pv test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.

Specomen: Whole blood

Time to result: 15 -30 minutes

Storage: 1-40 degree C for 24 months

Performance: Sensitivity: Pf-99.7%, Pv-95.5%

Specificity: 99.5 %

Optimal screening test for Plasmodium falciparum and Plasmodium vivax.
Jun-24-22
 
CAT No : 7D2343. A rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2)

Clear, dependable results in 15 minutes

Requires minimal training and no equipment

So easy it can be used at the lowest levels of health care service

Can use whole blood or serum/plasma

Collection can be by fingerstick or venipuncture

No refrigeration required

Storage conditions 2-30C
Jun-24-22
 
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.
Jun-24-22
 
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.
Jun-24-22
 
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.
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Jun-24-22
 
The Alere SD BIOLINE Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein II (HRP-II) antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood.

Optimal screening test for P.falciparum and other Plasmodium species

Ordering Information
Cat No. Description Type Pack size

05FK63I01 SD Malaria Device 1 Test
Jun-27-22
 
CAT No : PI19FRC25. First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40C.
Specimen Type- Whole Blood.
Oct-10-22
 
Product Details:
Number of Reactions(Preps)/Kit : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : 09FIL10D

Filariasis Ag Test Kit Contents:
Test Device in a foil pouch with desiccant
Disposable dropper
Instruction for use
Oct-10-22
 
Product Details:
Brand : Boditech Med Incorporated
Size : 25 Test
Samples : Whole blood
Sample volume : 75 Microliter
Cat No : CFPC-38
Storage Temperature ; 4 - 30 DegreeC
HbA1c
Assessing the level of glycated hemoglobin in the blood

This test is certified by NGSP (National Glycohemoglobin Standardization Program). It helps diabetic diagnosis, treatment, and prognosis by measuring the glycated hemoglobin concentration (%) in a small amount of blood over the past 3 months.

INTENDED USE

ichroma HbA1c is a fluorescence Immunoassay (FIA) for the quantitative determination of HbA1c(Hemoglobin A1c) in human whole blood. It is useful as an aid in management and monitoring of the longterm glycemic status in patients with diabetes mellitus. 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 antigen-antibody complex and leads to stronger intensity of fluorescence signal on detector antibody. Instrument for ichromaâ?¢ tests displays the content of glycated hemoglobin in terms of percent of the total hemoglobin in blood.
Oct-10-22
 
Product Details:
Brand : Boditech Med Incorporated
Size : 25 T
Samples : Human whole blood/serum/ plasma
Sample volume : 50 Microliter
stored at 4 - 30 DegreeC
Cat No : CFPC-65
Troponin I (Tn-I) Plus
Early diagnosis of myocardial infarction with high sensitivity

Troponin I (Tn-I) Plus can diagnose myocardial infarction and myocardial necrosis at an early stage with high sensitivity by accessing Tn-I level in the blood, thus can help prevent progression to more severe cases.

INTENDED USE:

ichroma Tn-I Plus is a Fluorescence Immunoassay (FIA) for the quantitative determination of cardiac troponin-I (Tn-I) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of acute myocardial infarction (AMI).

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 Tn-I concentration in the sample.

MATERIALS SUPPLIED :


REF CFPC-65

Components of ichroma Tn-I Plus

Cartridge Box:

- Cartridge 25

- 50L Capillary tube 25

- ID chip 1

- Instruction for Use 1

Buffer Box

For ichorma II

- Detector (Capped with plastic lid) 25

- Diluent 1

For ichroma 50

- Detector (Sealed with aluminum foil) 25

- Diluent 1
Oct-10-22
 
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
Oct-11-22
 
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.
Oct-11-22
 
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.
Oct-11-22
 
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%
Oct-11-22
 
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Bran : CTK BioTech
Sample Material : serum or plasma
Storage : 2-8 C
Cat. No : AE0310
The Dengue IgM ELISA Kit is a solid-phase enzyme-linked immunosorbent assay for the qualitative detection of IgM anti-dengue viruses (DEN1, 2, 3, 4) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of acute infection with dengue viruses.

TEST PRINCIPLE:

The Dengue IgM ELISA Kit is a solid-phase enzyme-linked immunosorbent assay based on the principle of the capture immunoassay methodology for the detection of IgM anti-dengue virus in human serum or plasma. The Dengue IgM ELISA Kit is composed of two key components: 1) Solid microwells pre-coated with mouse monoclonal anti-human IgM antibody. 2) Conjugate working solution composed of dengue antigen and HRP-anti-dengue conjugates. During the assay, the test specimen is first incubated in the coated microwell. IgM antidengue, if present in the specimen, binds to the anti-human IgM antibodies coated on the microwell surface, and any unbound specimen is then removed by a wash step. During a second incubation with HRP-anti-dengue conjugate working solution, the IgM anti-dengue absorbed on the surface of microwell binds to the conjugate through dengue antigen, forming a conjugate complex. Unbound conjugates are then removed by washing. After addition of the TMB substrate, the presence of the conjugate complex is shown by development of a blue color resulting from a reaction between the enzyme and substrate. This reaction is then quenched by addition of the Stop Solution, and the absorbance value for each microwell is determined using a spectrophotometer at 450/620-690 nm.

Accuracy of Detection :
A total of 491 patient specimens were collected from susceptible subjects and tested by Dengue IgM ELISA Kit and by a commercial leading brand EIA.


Relative Sensitivity: 90.8% (95% Confidence Interval = 85.5 - 94.4%) Relative Specificity: 95.9% (93.1 - 97.7%) Overall Agreement: 94.1% (91.6 - 95.9%).
Oct-11-22
 
Product Details:
Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample : serum or plasma
Storage : 2 - 8 C
Cat No : AE0610
INTENDED USE:

The TRUSTwell Syphilis Ab kit is a solid phase enzyme linked immunosorbent assay for the qualitative detection of antibodies (IgG, IgM, IgA) against Treponema pallidum (Tp) in human serum or plasma. It is intended for professional use only as an aid in the diagnosis of infection with Tp. Any reactive specimen with the TRUSTwell Syphilis Ab ELISA Test must be confirmed with alternative testing method(s) and clinical findings.

TEST PRINCIPLE:

The TRUSTwell Syphilis Ab ELISA Test is a solid phase enzyme linked immunosorbent assay based on the principle of the double antigen sandwich technique for the detection of antibodies to Tp in human serum or plasma. The TRUSTwell Syphilis Ab ELISA Test is composed of two key components: 1) Solid microwells pre-coated with recombinant Tp antigens; 2) Liquid conjugates composed of recombinant Tp antigens conjugated with horseradish peroxidase (HRP-Tp conjugates).

During the assay, the test specimen and HRP-Tp conjugates are incubated simultaneously with the coated microwells. Antibodies (IgG, IgM, or IgA) to Tp if present in the specimen, reacts to the Tp antigens coated on the microwell surface as well as the HRP-Tp conjugates, 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 absorbances are read using a spectrophotometer at 450 /620-690 nm.

Clinical Performance:

A total of 1132 patient specimens from susceptible subjects were tested by the TRUSTwell Syphilis Ab ELISA Kit.

Relative Sensitivity:100%,
Relative Specificity:99.8%,
Overall Agreement:99.82%.
Oct-11-22
 
Product Details:

Number of Reactions(Preps)/Kit 25T
Brand Abbott
Time To Result 15 Min
Result Time (Rapid Kits) 15 min
Sample Type Blood
Cat. No 05FK80
Bioline MALARIA Ag P.f/P.vTEST FOR PLASMODIUM FALCIPARUM AND PLASMODIUM VIVAX
The Bioline Malaria Ag P.f/P.v test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 (HRP-2) antigen of Plasmodium falciparum and Plasmodium lactate dehydrogenase (pLDH) of Plasmodium vivax in human whole blood.

BENEFITS

Differential diagnosis between Plasmodium falciparum and
Plasmodium vivax
Useful for the region where P.v and P.f are both dominant
Differentiate P.f mono infection from P.f/P.v co-infection
WHO prequalified
Specimen : Whole blood (5 l)
Time to result : 15 minutes (up to 30 minutes)
1-40C for 24 months
Performance:
P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5%
P.v (pLDH) : Sensitivity 95.5 %, Specificity 99.5%
Oct-11-22
 
Product Details:

Brand Abbott
Usage/Application Hospital
Results 30 min
Test Type Rapid Test
shelf life 24 months
Cat. No 05FK63I01
Bioline MALARIA Ag P.f/PanTEST FOR P.FALCIPARUM AND OTHER PLASMODIUM SPECIES
The Bioline Malaria Ag P.f/Pan test is a rapid, qualitative and differential test for the detection of histidine-rich protein 2 HRP2 antigen of Plasmodium falciparum and common Plasmodium lactate dehydrogenase (pLDH) of Plasmodium species in human whole blood.

Benefits:

Distinguish P.f infection from other species (P.v, P.m or P.o)
Useful in regions where all malaria species are circulating
WHO prequalified
Specimen : Whole blood (5 l)
Time to result : 15 minutes (up to 30 minutes)
1-40C for 24 months
Performance:
- P.f (HRP2) : Sensitivity 99.7 %, Specificity 99.5 %
- Pan (pLDH) : Sensitivity 95.5 %, Specificity 99.5 %
Oct-11-22
 
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%
Oct-11-22
 
Product Details:
Number of Reactions(Preps)/Kit 10
Brand Abbott
Result Time (Rapid Kits) 15 mins
Results 15 - 20 min
Cat. No 11FK45
Bioline DENGUE DUO (DENGUE NS1 Ag + IgG/IgM)TEST FOR DENGUE INFECTION
The Bioline Dengue Duo kit is a rapid, in-vitro immunochromatographic assay designed to detect both dengue virus NS1 antigen and IgG/IgM antibodies against dengue virus in human serum, plasma or whole blood. Bioline Dengue Duo rapid test contains two test devices (left side; Dengue NS1 Ag test, right side; Dengue IgG/IgM test).

Benefits:

Simultaneous detection of Dengue Ag & Ab
Cover all clinical stages from acute phase to convalescence phase of infection
Fast test result : 15~20 min
Convenient storage condition : 1~30C
Specification:
Performance
- Sensitivity : 92.4% (Dengue NS1 Ag), 94.2% (Dengue IgG/IgM)
- Specificity : 98.4%(Dengue NS1 Ag), 96.4% (Dengue IgG/IgM)
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