The Total Thyroxine (T4) ELISA is a solid-phase enzyme-linked immunosorbent assay based on the principle of the competitive ELISA technique for quantitative determination of Thyroxine in human serum.
The three main kit components are:
1) Solid microwells pre-coated with anti-T4
2) T4 Calibrators
3) Liquid T4 Enzyme Conjugate Mixture comprised of T4 labelled with horseradish peroxidase (T4-HRP)
Product Freature:
Analytical Sensitivity: 176 aµg/dL at 2-SD
Specificity: No cross-reactivity or interference with
d-Thyroxine 10 aµg/mL
d-Triiodothyronine 100 aµg/mL
Iodotyrosine 100 aµg/mL
Diiodotyrosine 100 aµg/mL
TBG 50 aµg/mL
Human Albumin 50 aµg/mL
Phenylbutazone 25 aµg/mL
Phenytoin 50 aµg/mL
ASA 500 aµg/mL
Acetaminophen 500 aµg/mL
Accuracy: correlation coefficient 0.98 with a reference method
Intra Assay Precision: CV a?¤ 5.9%
Inter Assay Precision: CV a?¤ 7.6%
Product Specification :
Anti-T4 Ab Coated Microwells
Total T4 Calibrators:
C1 (0 ng/mL)
C2 (2.0 ng/mL)
C3 (5.0 ng/mL)
C4 (10.0 ng/mL)
C5 (15.0 ng/mL)
C6 (25.0 ng/mL)
Total T4 Assay Control
Total T4 Enzyme Concentrate
Enzyme Buffer
Wash Buffer Concentrate
TMB Substrate
Stop Solution
Product Insert
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.
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.
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.
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%
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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 %
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%
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)
Product Details:
Number of Reactions(Preps)/Kit 100T
Brand Abbott
Usage/Application Hospital
Result Time (Rapid Kits) 30 Min
Sample Type Blood
CAT No : 7D2343
DETERMINE HIV-1/2
Rapid HIV screening tested by billions and proven by practice. Determine HIV-1/2 test detects a wide variety of HIV subtypes (refer to IFU). This versatility helps healthcare workers across the world diagnose individual infection, monitor HIV prevalence, and enable fast linkage to care.
With its simple one-step procedure for serum/plasma or two-step procedure for whole blood, the Determine HIV-1/2 is quick and easy to use, delivering clear, dependable results in just 15 minutes.
PRODUCT INFORMATION
Method: Lateral flow
Time to results: 15 minutes
Storage conditions: 2-30C (36-86F)
Shelf-life: 18 months
Sample types: Serum/Plasma/Whole blood
SPECIFICITY
Overall 99.75%
Number of Reactions(Preps)/Kit 25T
Brand Premier
Result Time (Rapid Kits) 15 - 20
Certified WHO Aproved
CAT No : I20FRC25
First Response HIV 1+2 / Syphilis Combo Card Test is intended for use by healthcare professionals and trained user. It is a rapid, qualitative screening, in vitro diagnostic test for the detection of antibodies (IgG & IgM) specific to HIV (type 1 & 2) and Treponema pallidum in human serum, plasma or venous and capillary whole blood.
Sensitivity: 100%
Specificity: 100%
Storage at 4-30 C
Rapid Result time - 15 to 25 Minutes.
Detects antibodies specific to HIV and Syphilis.
Specimen Type Whole blood, Serum, Plasma
Shelf Life: 24 Months
Product Details:
Number of Reactions(Preps)/Kit 30 T
Brand Premier
Result Time (Rapid Kits) 15 min
CAT No; PI05FRC30
Certified WHO Aproved
First Response HIV 1-2.O Card Test (Ver. 2.0) is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative screening, in vitro diagnostic test for detection of antibodies specific to HIV-1 (including Group O) and HIV-2 in human serum, plasma or venous and capillary whole blood.
Product specifications :
Sensitivity: 100%
Specificity: 100%
Detects antibodies specific to HIV-1 (including Group O) and HIV-2.
Rapid Result time - 15 to 25 Minutes.
Storage at 4-30 C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
Number of Reactions(Preps)/Kit 25 T
Brand Premier
Result Time (Rapid Kits) 20 - 25 Min
Certified WHO Approved
CAT No; PI08FRC25
First Response Syphilis Anti-TP Card Test is intended for use by healthcare professionals and qualified laboratory personnel. It is a rapid, qualitative, screening, in vitro diagnostic test for the detection of antibodies of all classes specific to Treponema pallidum in human serum, plasma or Venous or capillary whole blood.
Product specifications :
100% - Specificity
100% - Sensitivity
Detects antibodies specific to Treponema pallidum
Rapid Result time within 20-25 Minutes
Storage at 4-30 C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
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
Product Details:
Brand Abon
No of test per kit 100
HCG Urine Pregnancy Test measures the presence of the pregnancy hormone (HCG) in your urine for the early detection of pregnancy.
Number of Reactions(Preps)/Kit 100
Brand Abbott
Usage/Application Hospital
By detecting early markers of Hepatitis B infection, the Alere Determine HBsAg helps to diagnose acute infection and confirm chronic infection - allowing healthcare professionals to initiate prompt and appropriate follow-up action for infected patients.
Rapid in-vitro qualitative ICT for detection of HBsAg
Sample Type: Serum/Plasma/Whole Blood
Sample Volume: 50µL
Early marker of infection- helps in diagnosis
Facilitates appropriate follow-up of infected patients
Collection can be done by fingerprick or venipuncture
Clear, dependable results in 15 minutes
Quick Reference Card for the detection of HBsAg in
In primary infection with the dengue virus, IgM antibody becomes detectable about five days after disease onset, when circulating virus declines in the blood. IgM level rises quickly to peak at about 2 weeks and declines to undetectable levels after 2-3 months In secondary infections, IgM response is typically at a lower level compared to that in a primary infection. Early diagnosis of dengue infection (especially in primary dengue infection) High accuracy with all dengue serotypes (DEN1,2,3, and 4) Simple and easy to use: All necessary reagents included in the kit Shelf life and storage temperature: 18 months from the date of manufacturing at 2-8 C Included in the WHO Bulk Procurement Scheme Performance: Sensitivity 96.4 %, Specificity 98.9 % (vs. HAI test).
Product Details:
Brand ACON
Size 50 Test
Cat. No ACKCRDPC3
Product Description :
Acon Pregnancy Test Strip (HCG) is a one step pregnancy test kit containing test strip. The urine sample is to be collected in a clean, dry container and almost half test strip should be dropped inside the container. The first urine sample of the day is preferred. The pack insert should be thoroughly read before use. To know how to use and read test results. Acon pregnancy test strip detects pregnancy in just 5 minutes.
Features & Specifications :
One Step Pregnancy Test Strip
Easy to Use
Quick Result in just 5 minutes
Pack of 3 Test Strips
For more info, please refer the product pack for usage instructions
Product Details:
Number of Reactions(Preps)/Kit 20T
Brand Abbott
Result Time (Rapid Kits) 10 -20 min
Sample Material Fecal
Cat. No 14FK10
Bioline* Rotavirus test is an immunochromatographic assay for the detection of Group A rotavirus in human fecal specimens. The test utilizes two kinds of antibody in a solid phase sandwitch immunochromatography to detect group specific proteins, including the major inner capsid protein, present in Group A rotaviruses.
Early detection of rotavirus antigen group A all serotype
Shelf life and storage temperature: 18 months from the date of manufacturing at1-30 C
Performance: Sensitivity : 94 %, Specificity 98.3 % (vs. RT-PCR)
Number of Reactions(Preps)/Kit : 25T
Brand : Abbott
Usage/Application : Hospital
Results : 15 min
Sample type : Blood
Cat. No : 08FK50
Bioline TB Ag MPT64TEST TO DISCRIMINATE BETWEEN M. TUBERCULOSIS COMPLEX AND MOTT(NTM)
Bioline TB Ag MPT64 is a immunochromatographic identification test for the M. Tuberculosis complex. Biochemical, immunological and molecular biological characterization of Mycobacterium tuberculosis has led to the identification of several antigens which may be useful in the development of improved diagnostic methods in order to discriminate between the M. tuberculosis complex and mycobacteria other than M. tuberculosis (MOTT bacilli). 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.
Performance
Sensitivity: 98.6 %, Specificity: 100 % (vs. Isolated culture method)
Simple, rapid assay using mouse monoclonal anti-MPT64
Rapid discrimination between the M. tuberculosis complex and other mycobacterium
Identification of the M. tuberculosis complex in combination with culture systems based on liquid media
Specimen : Solid cultures (colony, condensation fluid) or liquid cultures
Time to result : 15 minutes
1-30 C for 18 months
Product Details:
Number of Reactions(Preps)/Ki : 25T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits): 10-15 mins
CAT No : RK055-25
STANDARD Q COVID-19 Ag is a rapid Immunochromatographic assay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
Qualitatively detects specific antigens to SARS-CoV-2 present in Human Nasopharynx.
The test should be used as an aid in early diagnosis of symptomatic cases in healthcare setting having ILI.
Validated by ICMR & AIIMS
Sensitivity of 84.38 % & Specificity of 100%
Sample Type- Human Nasopharyngeal swab (No other sample recommended)
Results in 15-30 mins
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