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Top Supplier Cities : -   Chennai   Mumbai  
Oct-12-22
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Product Details:
Number of Reactions(Preps)/Kit : 250 Rxns Per Box
Brand : HiMedia
Storage Temperature : 15 DegreeC to 25 DegreeC
Elution Volume : 50 to 80 microliter
Cat. No : MB615
Description
This kit carries out efficient extraction of viral RNA from wide range of viral strains like Dengue, Chikungunya and viral pathogen of animals. Sample is first lysed under the highly denaturing conditions provided by Buffer HRL to inactivate RNases and to
Used For
HiPur Viral RNA Miniprep Purification Kit can be used for isolation of viral RNA from a wide variety of viruses, but performance may vary depending on virus type
Oct-12-22
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Product Details:
Brand : SD Biosensor
Test Method : Antigen Test
Pack Type : 25
Cat. No : RK081-25
Oct-12-22
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Product Details:
Brand ; Genbody
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Packaging Size : 25 Test Kits /Box
CAT No : COVAG025
GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in nasopharyngeal and oropharyngeal swab from human.
Oct-12-22
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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
Oct-12-22
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Product Details:

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
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Oct-11-22
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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
Oct-11-22
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Product Details:

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

human serum/plasma or whole blood

Ordering Information

Cat No. Description Type Pack size

7D2543 Alere Determine HBsAg Strip 100 Tests
Oct-11-22
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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.
Oct-11-22
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Product Details:

Number of Reactions(Preps)/Kit 30T
Brand Abbott
Usage/Application Hospital
Result Time (Rapid Kits) 15 mins
Cat. No 02FK10I30
Bioline HCVHEPATITIS C VIRUS TEST
When speed matters, choosing a highly sensitive rapid HCV test with a safe fingerstick procedure can make a difference.

In the global effort to eliminating viral hepatitis, fast detection in a wide range of settings and linkage to care are critical for achieving successful outcomes

Bioline HCV test is a immunochromatographic rapid test for the qualitative detection of antibodies specific to HCV in human serum, plasma or whole blood.

Specification:

Specimen :
- Serum, Plasma, Whole Blood (10 �¼l) for 02FK10, 02FK10CE, 02FK16, 02FK16CE, 02FK17, 02FK17CE, 02FK11
- Serum or Plasma (10 l) for 02FK12
Sensitivity :
- 99.3% (95% CI: 97.9 - 99.8%) for 02FK10CE, 02FK16CE, 02FK17CE
- 99.3% (95% CI: 96.1 - 99.9%) for 02FK10, 02FK16, 02FK17
- 100 % (97.6 - 100 %) for 02FK11, 02FK12
Specificity :
- 100% (95% CI: 99.7 - 100 %) for 02FK10CE, 02FK16CE, 02FK17CE
- 98.1% (95% CI: 94.5 - 99.4%) for 02FK10, 02FK16, 02FK17
- 99.4 % (98.7 - 99.7 %) for 02FK11, 02FK12
Shelf life: 24 months at 1-30C
Qualitative immunochromatographic assay
Recombinant HCV core, NS3, NS4, NS5 Ag used as capture materials
Oct-11-22
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Product Details:

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
Oct-11-22
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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
Oct-11-22
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Product Details:

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
Oct-11-22
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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%
Oct-11-22
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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)
Oct-11-22
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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
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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
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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
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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
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Product Details:

Number of Reactions(Preps)/Kit : 50T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
Sample Type : Blood
Country of Origin : Made in India
STANDARD E Dengue NS1 Ag ELISA analyzes Dengue NS1 antigens in serum and plasma using enzyme linked immunosorbent assay.

Simple and easy to use: All necessary reagents included in the kit
Highest accuracy with all dengue serotypes(DEN1,2,3, and 4)
Able to detect antigens in samples with high sensitivity and specificity
Performance
Sensitivity : 91.4% (181/198) / Specificity : 98.2% (221/225)
Oct-11-22
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Product Details:

Number of Reactions(Preps)/Kit : 96 Wells
Brand : CTK BioTech
Sample ; Serum
Storage : 2-8 C
Cat No : E1030
The RecombiLISA TSH ELISA is a solid phase enzyme linked immunosorbent assay for the quantitative determination of the levels of Thyroid Stimulating Hormone (TSH) in human serum.

The RecombiLISA TSH ELISA is intended for professional use as an aid in the diagnosis of thyroid dysfunction. TSH values should not be the only factor in the determination of thyroid status, and all other available clinical and epidemiological information should be considered for an accurate diagnosis.

Recommended for use:

Any person presenting with signs or symptoms of hypo or hyperthyroidism
Any person presenting with an enlarged thyroid gland (goiter)
Pregnant women for first trimester screening
Any person requiring regular monitoring of treatment
Normally, thyroid function is first assessed by detection of TSH levels in the blood.

The monoclonal anti-TSH antibody coated on the surface of the microwells specifically recognizes the junction between the �± and �² subunits. The HRP-conjugated monoclonal anti-TSH antibody detects the �² subunit only.

Combining the measurement of TSH with the thyroid hormones (T3/T4) can provide more information for the determination of thyroid status.

Product Features :

Sensitivity: Detects TSH levels as low as 0.035 �µIU/mL
Specificity: No cross reactivity detected with related hormones: FSH, LH and hCG
Linearity: 1:128 dilution on 36 IU/mL sample
Precision: intra assay precision: CV 7.5%; inter assay precision: CV 8.0 %
Accuracy: R2= 0.986 against Roche TSH Chemiluminescence Immunoassay
Hook effect: No hook effect up to 8000 IU/mL
Interference: not affected by Hemoglobin 500mg/dL, Diltiazem 15uM, Bilirubin 20 mg/dL, Erythromycin 81.6uM, Triglycerides 3g/dL, Verapamil 4.4uM, HAMA 52.5ng/mL, T3 100ng/mL, RF 215IU/mL, T4 100ug/dL, Acetaminophen 1324uM
Calibration: Human TSH WHO 3rd International Standards (81/565 NIBSC)
Calibrators: 0, 0.5, 2.0, 5.0, 10, 20, 40 �µIU/mL in biological matrix
Shelf life: 18 months
Assay time: 80 minutes.

Product Specifications:
Anti-TSH Ab coated microwells
TSH standard S1
TSH standard S2
TSH standard S3
TSH standard S4
TSH standard S5
TSH standard S6
TSH standard S7
HRP-anti-TSH conjugates
TMB substrate
Wash buffer (30X concentrate)
Stop solution
ELISA working sheet
Product insert
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