The FactView Dengue NS1 Antigen test is a diagnostic assay used for the rapid detection of the non-structural protein 1 (NS1) antigen produced by the dengue virus. Here's more information about this type of diagnostic test:
Purpose: The test is used for the early detection of dengue virus infection. Dengue is a mosquito-borne viral infection caused by four closely related viruses (DENV-1, DENV-2, DENV-3, and DENV-4) transmitted by Aedes mosquitoes.
Principle: The FactView Dengue NS1 Antigen test is an immunochromatographic assay that detects the presence of the NS1 protein in a patient's blood sample. NS1 is a viral protein produced during acute dengue infection and can be detected in the bloodstream during the early stages of the disease.
Components: The test typically includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific antibodies for capturing the NS1 antigen.
Procedure: The test procedure involves collecting a small amount of blood from the patient (usually obtained via finger prick) and applying it to the sample well of the test cassette. Buffer solution is then added, allowing the blood sample to migrate along the test strip. Results are typically visible within 15-20 minutes.
Interpretation: The appearance of colored lines on the test strip indicates the presence or absence of the NS1 antigen. A visible line in the control region indicates that the test is valid. Additional lines in the test region(s) indicate positive results for NS1 antigen.
Sensitivity and Specificity: The FactView Dengue NS1 Antigen test demonstrates high sensitivity and specificity for detecting dengue virus infection during the early stages of illness. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings.
Utility: Rapid diagnostic tests like the FactView Dengue NS1 Antigen test provide a quick and convenient method for diagnosing dengue virus infection in resource-limited settings, where access to laboratory facilities and molecular testing may be limited.
Limitations: While rapid diagnostic tests are valuable tools for dengue diagnosis, they have limitations compared to more sensitive methods such as nucleic acid amplification tests (NAATs) or virus isolation. Factors such as test storage conditions, operator technique, and the stage of infection can influence test performance.
A "premium tonometer" typically refers to a high-quality, advanced device used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, which is an important indicator of eye health and is particularly crucial in conditions such as glaucoma.
Premium tonometers often incorporate advanced technology and features to provide accurate and reliable measurements of intraocular pressure. Here are some characteristics commonly associated with premium tonometers:
Accuracy: Premium tonometers are designed to provide highly accurate measurements of intraocular pressure. They often use sophisticated sensors and calibration methods to ensure precision.
Ease of Use: These tonometers are usually user-friendly, with intuitive interfaces and ergonomic designs. They may feature automated measurement functions to streamline the testing process.
Versatility: Premium tonometers may offer versatility in terms of measurement methods. For example, some tonometers use applanation tonometry, where a small probe gently flattens a portion of the cornea to measure pressure, while others may use techniques such as air puff tonometry or rebound tonometry.
Data Management: Many premium tonometers include features for storing and managing measurement data. This may include digital storage capabilities, connectivity options for transferring data to electronic medical records systems, or integration with software for analysis and reporting.
Quality Construction: Premium tonometers are typically constructed with durable materials and undergo rigorous quality control to ensure reliability and longevity.
Calibration: These devices often have built-in calibration systems or mechanisms to maintain accuracy over time. Regular calibration ensures that the measurements remain consistent and reliable.
Professional Use: Premium tonometers are commonly used in clinical settings by ophthalmologists, optometrists, and other eye care professionals who require precise intraocular pressure measurements for diagnostic and monitoring purposes.
A "premium tonometer" typically refers to a high-quality, advanced device used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, which is an important indicator of eye health and is particularly crucial in conditions such as glaucoma.
Premium tonometers often incorporate advanced technology and features to provide accurate and reliable measurements of intraocular pressure. Here are some characteristics commonly associated with premium tonometers:
Accuracy: Premium tonometers are designed to provide highly accurate measurements of intraocular pressure. They often use sophisticated sensors and calibration methods to ensure precision.
Ease of Use: These tonometers are usually user-friendly, with intuitive interfaces and ergonomic designs. They may feature automated measurement functions to streamline the testing process.
Versatility: Premium tonometers may offer versatility in terms of measurement methods. For example, some tonometers use applanation tonometry, where a small probe gently flattens a portion of the cornea to measure pressure, while others may use techniques such as air puff tonometry or rebound tonometry.
Data Management: Many premium tonometers include features for storing and managing measurement data. This may include digital storage capabilities, connectivity options for transferring data to electronic medical records systems, or integration with software for analysis and reporting.
Quality Construction: Premium tonometers are typically constructed with durable materials and undergo rigorous quality control to ensure reliability and longevity.
Calibration: These devices often have built-in calibration systems or mechanisms to maintain accuracy over time. Regular calibration ensures that the measurements remain consistent and reliable.
Professional Use: Premium tonometers are commonly used in clinical settings by ophthalmologists, optometrists, and other eye care professionals who require precise intraocular pressure measurements for diagnostic and monitoring purposes.
An "ECO tonometer" is a type of tonometer used to measure intraocular pressure (IOP) in the eye. Intraocular pressure is the fluid pressure inside the eye, and it's an important aspect of eye health to monitor, especially in conditions like glaucoma, where elevated intraocular pressure can lead to optic nerve damage and vision loss.
The "ECO" in ECO tonometer might stand for "Electronic Contact Ophthalmodynamometer." This type of tonometer typically uses electronic sensors and probes to measure intraocular pressure. Contact Method: ECO tonometers usually involve direct contact with the surface of the eye. The device gently touches the cornea to measure the pressure within the eye.
Electronic Sensors: These tonometers utilize electronic sensors to detect changes in pressure. When the probe makes contact with the cornea, it measures the force required to slightly flatten the cornea, providing a measurement of intraocular pressure.
Digital Display: ECO tonometers often have a digital display that shows the measured intraocular pressure in millimeters of mercury (mmHg) or another applicable unit.
Accuracy and Precision: These tonometers are designed to provide accurate and precise measurements of intraocular pressure, which is essential for monitoring eye health and diagnosing conditions like glaucoma.
WHO Approved, 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 4-30C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
3646 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
The MagMAX Viral/Pathogen Nucleic Acid Isolation Kit is designed to recover RNA and DNA from virus and gram-negative bacteria in samples such as blood, swabs, urine, and viral transport media (VTM). The kit utilizes MagMAX magnetic-bead technology, ensuring reproducible recovery of high-quality nucleic acid compatible with a broad range of applications, including real-time PCR, digital PCR, and next-generation sequencing.
Features of the MagMAX Viral/Pathogen Nucleic Acid Isolation Kit include:
Automation-ready protocols designed for the KingFisher Flex and KingFisher Duo Prime systems
Fast procedure allows for 96 samples to be processed in <30 minutes
Flexible protocol accommodates sample volume inputs from 200 µL to 2 mL of biofluids or transfer media
No need for carrier RNA
Elution volumes ranging from 50 to 100 µL
Cat No : 09N77-095. The Abbott RealTime SARS-C0V-2 assay is an Emergency Use Authorization (EUA) test authorized by the U.S. FDA for use by authorized laboratories, using real-time (RT) polymerase chain reaction (PCR) technology for the qualitative detection of nucleic acids from the SARS-CoV-2 virus and diagnosis of SARS-CoV-2 virus infection from individuals meeting CDC clinical and/or epidemiological testing criteria.
STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CTK Biotech's, CE Certified , the OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
Product Specification:-
Brand Name : CTK Biotech
Pkg Qty : 1
Number Of Items : 30
Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action
Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
CAT No : RK026-30. STANDARD Q HBsAg performs qualitative analysis by specifically detecting the surface protein antigens of hepatitis B virus in serum, plasma and whole blood using immunochromatography. With a simple test method, hepatitis B infection can be discriminated early, and with its high sensitivity and specificity, the screening test result can be obtained within 20 minutes.
Easy to use, Easy to read and interpret
Room temperature storage
Performance
Sensitivity : 100% (43/43) / Specificity : 100% (162/162)
CAT No : RK025-40. One step, rapid immunothematographic test for the differential detection between Plasmodium falciparum Histidine- Rich Protein II (HRP II) and Plasmodium species (P. falciparum , P vivax P. ovale, P. malariae) lactate dehydrogenase (pLDH) in human whole blood
Kit Contents:
Standard Q Malaria Pf/PV Ag cassette x 40
Specimen transfer device 3 microlitre x 40
Butter bottle 3m1 x 02
Instructions for use x 01
STANDARD Q Malaria P.f Ag qualitatively analyzes Plasmodium falciparum and CAT Cat.No : RK025-40. Plasmodium vivax antigens in whole blood using immunochromatography. The target antigen is Histidine-Rich Protein II (HRP-II) of Plasmodium faciparum and plasmodium lactate dehydrogenase (pLDH) of Plasmadium vivax, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity
Advantage:
Distinguish the infection between P.falciparum and P.vivax
Optimized on-site diagnosis with the small diagnostic kit
Able to read positive/negative infections fast and accurately with a little blood (5�µl)
Room temperature storage.
Cat No : PI19FRC25. 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 4-30C
Specimen Type Whole blood, serum, plasma
Shelf Life: 24 Months
Cat No : 11FK50. Bioline DENGUE NS1 Ag TEST FOR EARLY CLINICAL PHASE OF DENGUE INFECTION
Bioline Dengue NS1 Ag rapid test is an in vitro immunochromatographic assay designed to detect Dengue virus NS1 antigen in human serum, plasma or whole blood.
Product not available in all countries. Please check with your local sales representative regarding availability in your area.
Benefits:
Diagnosis of early acute dengue infection by detecting dengue NS1 antigen
Dengue NS1 antigen can be detected from 1 day after onset of fever
Specimen : Serum, plasma or whole blood (100�¼l)
Test result : 15~20 minutes
Specification:
Sensitivity 92.4%, Specificity 98.4%
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.
â?¢ 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)
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 : 10T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15 min
CAT No : RK013-10
One step, rapid, immunochromatographic test for the detection of IgM/IgG antibodies to four serotypes of dengue virus (DEN-1, DEN-2, DEN-3 and DEN-4) & Dengue virus NS1 antigen in human serum, plasma or whole blood.
Kit Contents:
Standard Q Dengue Ag Ab Duo cassette x 10
Specimen transfer device 10ml x 10
Butter bottle 4ml x 01
Instructions for use x 1
STANDARD Q Dengue Duo test is an immunochromatographic assay for the detection of NS1 antigen and Dengue virus-specific IgM and IgG antibodies in human serum, plasma and whole blood. By detecting the NS1 antigen, not only the initial infection can be detected, but also Dengue virus-specific IgM and IgG can be detected at the same time. Screening test results can be obtained within 15 minutes with high sensitivity and specificity.
Product Details:
Number of Reactions(Preps)/Kit :20T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 15min
CAT No : RK012-20
One step, rapid, immunochromatographic test for the detection of Dengue IgMlIgG antibodies to four senatypes of dengue virus (DEN-I, DEN-2. DEN-3 and DEN-4) in human serum, plasma or whole blood.
Kit Contents:
Standard Q Dengue IgM IgG cassette x 20
Specimen transfer device 10ml x 20
Butter bottle 4ml x 01
Instructions for use x 1
STANDARD Q Dengue IgM/IgG qualitatively analyzes IgM and IgG antibodies specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting IgM and IgG specific to Dengue virus, the primary and secondary Dengue virus infections can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Advantage:
Differential detection of IgG and IgM antibodies
Easy to use, Easy to read and interpret
Room temperature storage
Able to read positive/negative infections fast and accurately with a little amount of sample (10 �µl)
3646 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
