The FactView HBsAg Strip is a diagnostic assay used for the qualitative detection of hepatitis B surface antigen (HBsAg) in human serum or plasma samples. Here's more information about this type of diagnostic test:
Purpose: The test is used for the diagnosis of hepatitis B virus (HBV) infection. HBsAg is a protein present on the surface of HBV particles and is the earliest serological marker of acute HBV infection. Detection of HBsAg indicates active HBV infection.
Principle: The FactView HBsAg Strip is typically an immunochromatographic assay that utilizes specific antibodies to capture HBsAg molecules in a patient's serum or plasma sample. The test is based on the principle of antigen-antibody binding, where HBsAg in the sample binds to specific antibodies immobilized on the test strip, resulting in the formation of visible test lines.
Components: The test kit usually includes test strips, sample droppers, buffer solutions, and desiccants. The test strips contain specific reagents and antibodies for capturing HBsAg from the serum or plasma sample.
Procedure: The test procedure involves collecting a small amount of serum or plasma from the patient and adding it to the sample well of the test strip. Buffer solution is then added, allowing the 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 HBsAg in the patient's serum or plasma sample. A visible line in the control region indicates that the test is valid. An additional line in the test region indicates a positive result for HBsAg.
Sensitivity and Specificity: The FactView HBsAg Strip demonstrates high sensitivity and specificity for detecting HBsAg in serum or plasma samples. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings.
Utility: The qualitative detection of HBsAg provides valuable information for diagnosing HBV infection, assessing disease status, and guiding patient management decisions. HBsAg positivity indicates active viral replication and infectiousness.
Limitations: While HBsAg testing is a valuable diagnostic tool, it has limitations, including the potential for false-positive results in low-prevalence populations and the inability to differentiate between acute and chronic HBV infection based solely on HBsAg positivity.
Overall, the FactView HBsAg Strip is an important tool for diagnosing HBV infection, allowing for timely intervention and management of patients with HBV-related liver disease. It aids in the prevention of HBV transmission and the implementation of control measures to reduce the burden of hepatitis B worldwide.
The FactView Typhoid IgG/IgM Rapid Test Kit is a diagnostic assay used for the qualitative detection of IgG and IgM antibodies specific to Salmonella typhi, the bacterium that causes typhoid fever. Here's more information about this type of diagnostic test:
Purpose: The test is used for the rapid diagnosis of typhoid fever, a bacterial infection caused by Salmonella typhi. Typhoid fever is characterized by fever, abdominal pain, headache, and other symptoms, and it can lead to serious complications if not treated promptly.
Principle: The FactView Typhoid IgG/IgM Rapid Test Kit is an immunochromatographic assay that detects the presence of IgG and IgM antibodies in a patient's blood sample. IgM antibodies are typically produced during the acute phase of infection, while IgG antibodies are produced later during the convalescent phase.
Components: The test kit usually includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific antigens for capturing IgG and IgM antibodies against Salmonella typhi.
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 IgG and IgM antibodies against Salmonella typhi. A visible line in the control region indicates that the test is valid. Additional lines in the test region(s) indicate positive results for IgG and/or IgM antibodies.
Sensitivity and Specificity: The FactView Typhoid IgG/IgM Rapid Test Kit demonstrates sensitivity and specificity for detecting typhoid fever. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings.
Utility: The rapid detection of IgG and IgM antibodies against Salmonella typhi provides valuable information for diagnosing acute or recent typhoid fever infections, determining immune status, and guiding patient management decisions.
Limitations: While rapid diagnostic tests are useful for typhoid fever diagnosis, they have limitations compared to more sensitive methods such as blood culture or molecular testing. Factors such as test sensitivity, specificity, and the timing of specimen collection can influence test performance.
Overall, the FactView Typhoid IgG/IgM Rapid Test Kit is an important tool for diagnosing typhoid fever, allowing for timely patient management and implementation of control measures. However, results should be interpreted carefully in conjunction with clinical evaluation and other laboratory tests.
The FactView Dengue IgG/IgM Antibody Combo test is a diagnostic assay used for the simultaneous detection of both IgG and IgM antibodies produced by the immune system in response to dengue virus infection. Here's more information about this type of diagnostic test:
Purpose: The test is used for the diagnosis of dengue virus infection in patients presenting with symptoms consistent with dengue fever or other dengue-related illnesses. 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 IgG/IgM Antibody Combo test is an immunochromatographic assay that detects the presence of both IgG and IgM antibodies in a patient's blood sample. IgM antibodies are typically produced during the acute phase of infection, while IgG antibodies are produced later during the convalescent phase and provide long-term immunity.
Components: The test typically includes test cassettes, sample droppers, buffer solutions, and desiccants. The test cassettes contain pre-coated membranes with specific antigens for capturing IgG and IgM antibodies.
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 IgG and IgM antibodies. A visible line in the control region indicates that the test is valid. Additional lines in the test region(s) indicate positive results for IgG and/or IgM antibodies.
Sensitivity and Specificity: The FactView Dengue IgG/IgM Antibody Combo test demonstrates high sensitivity and specificity for detecting dengue virus infection. However, like all diagnostic tests, false-positive and false-negative results are possible and should be interpreted in conjunction with clinical findings.
Utility: The rapid detection of IgG and IgM antibodies against dengue virus provides valuable information for diagnosing acute or recent dengue virus infection, determining immune status, and guiding patient management decisions.
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.
1482 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
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
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)
1482 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
