The PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is an immunofluorescent sandwich assay. It can detect the virus with very high sensitivity and specificity.
When the sample is applied to the sample wells, SARS-CoV N protein and labeled antibody complexes are formed and travel up the strip. The labeled microsphere fluorescent probe reagent is used to form a visible red line with a matched UV flashlight.
The presence of SARS-CoV-2 will be indicated by a visible red test line (T) in the result window. The membrane is pre-coated with Chicken IgY on the control (C) line. Control (C) line appears in each result window when the sample has flowed through the strip.
The PocRoc SARS-CoV-2 Antigen Rapid Test Kit(Colloidal Gold)is used for qualitative detection of SARS-CoV-2 virus nucleocapsid protein, which is an important conserved structural protein of SARS-CoV-2 in human nasal/ oropharyngeal samples.
The detection of SARS-CoV-2 nucleocapsid protein antigen can be used to assist the diagnosis of novel coronavirus infection and is helpful for the early detection of novel coronavirus pneumonia infection in the latent period.
TBG SARS-CoV-2 Neutralizing Antibody Qualitative Rapid Test(colloidal gold) Now with the detection before and after vaccination, TBG''s company has a neutralizing antibody detection reagent, that it can be used as the effective rate detection of antibody before and after vaccination. No matter how the vaccine is administered, The Neutralizing Antibody Qualitative Rapid Test will be used. Our test kits for COVID-19 as below are still effective to detect the infection of new COVID-19 variant B.1.1.7and The new variant has no effect on the detection performance of products
SARS-CoV-2 IgG/IgM Rapid Test Kit
Intended Use: To detect IgM and IgG antibodies against N and S protein of SARS-CoV-2 in whole blood, serum and plasma
Product Format:Â 25 tests/kit
Kit Contents: test card, diluent, capillary, lancet, and instruction for use.
Storage/Stability: 2 C to 30C for 12 months.� eproducibility /Precision
100% Concordant across 3 lots with CV ±5%
Performance Comparison (A)
China Validation Test
Positive Samples 100 / 102
Sensitivity: 98.04%
Negative Samples 491/492
Specificity: 99.80%
Overall Accuracy: 99.49%
Performance Comparison (B)
Positive Samples 23 / 25
Sensitivity: 92%
Negative Samples 25 / 25
Specificity: 100%
Overall Accuracy: 96%
SARS-CoV-2 Antigen Rapid Test (Nasopharyngeal swab samples)
SARS-CoV-2 Antigen Rapid Test Saliva)
We have two fast screening reagents for routine detection. One is the antibody iggigm detection reagent (that is, blood for three minutes) One is antigen rapid screening test reagent (the same is three minutes can use nasal mucosa, oral mucosa, and saliva three detection methods) 1.SARS-CoV-2 antigen testing can detect infection earlier than antibody testing 2.SARS-CoV-2 antigen testing can detect SARS-CoV-2 and all mutant virus strains 3.Easy operation and quick results 4.The result is clear. C-line and T-line determines the infection and the result is easy to read 5.The colloidal gold method has stable performance and is not interfered by environmental and experimental conditions 6.Application: for human throat swab , nasal swab and sputum extract Our test kits for COVID-19 as below are still effective to detect the infection of new COVID-19 variant B.1.1.7and The new variant has no effect on the detection performance of products
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Rapid Antigen and Antibody test kit covid 19
Manufacturer: Shenzhen Lvshiyuan Biotechnology Co., Ltd / Green Spring Brand
The time required: 15 -20 minutes
Detect the virus 3 days after the infection
Accuracy: High
Specificity: High
Cost Saving : Low cost
HCG Test is an immunochromatographic assay designed for qualitative determinatrion of human chronic gonadotropin (hCG) in urine for the detection of pregnancy. Human chorionic gonadotropin is a glycopeptide hormone produced by the placenta during pregnancy. The apprearance and rapid rise in the concentration of hCG in the woman''s urine makes it good pregnancy marker. Usually, concentration of hCG in urine is at least 25mlU/ml within seven to ten days after conception.
Justifying our reputation in this market, we are readily immersed in the arena of offering to our patrons a broad consignment of HCG Tests Kits.
Minimum order - 5000 units.
Port - Shanghai, Ningbo
Payment - T/T, L/C
Coronavirus Ag rapid test cassette (swab)
* Rapid testing for SARS-Cov-2 antigen within 15 minutes
* Facilitates patient treatment decisions quickly
* Simple time saving procedure
* All necessary reagents provided & no equipment needed
* High sensitivity and specificity
20 tests per kit.
Storage - 2 to 30 degrees C.
Shelf life - 24 months
Specimen type - Nasal or throat swab.
The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogs feces or vomit specimen.
Assay Time: 5-10 minutes
The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen.
The kit can be stored at room temperature (4-30C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight.
TEST PROCEDURE
-Collect dogs fresh feces or vomit with the cotton swab from dogs anus or from the ground.
-Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction.
-Take out the test device from the foil pouch and place it horizontally.
-Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device.
-Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.
INTERPRETATION OF RESULTS
-Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague.
-Negative (-): Only clear C line appear. No T line.
-Invalid: No colored line appears in C zone. No matter if T line appears.
PRECAUTIONS
-All reagents must be at room temperature before running the assay.
-Do not remove test cassette from its pouch until immediately before use.
-Do not use the test beyond its expiration date.
-The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
-All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states.
LIMITATION
Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.
The Canine Parvo Virus Antigen Rapid Test is a lateral flow immunochromatographic assay for the qualitative detection of canine Parvo virus antigen (CPV Ag) in dogâ??s feces or vomit specimen.
Assay Time: 5-10 minutes
The Canine Parvo Virus Antigen Rapid Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window for the observation of assay running and result reading. The testing window has an invisible T (test) zone and a C (control) zone before running the assay. When the treated sample was applied into the sample hole on the device, the liquid will laterally flow through the surface of the test strip and react with the pre-coated monoclonal antibodies. If there is CPV antigen in the specimen, a visible T line will appear. The C line should always appear after a sample is applied, which indicates a valid result. By this means, the device can accurately indicate the presence of Parvo virus antigen in the specimen.
The kit can be stored at room temperature (4-30�°C). The test kit is stable through the expiration date marked on the package label. DO NOT FREEZE. Do not store the test kit in direct sunlight.
TEST PROCEDURE
-Collect dogâ??s fresh feces or vomit with the cotton swab from dogâ??s anus or from the ground.
-Insert the swab into the provided assay buffer tube. Agitates it to get efficient sample extraction.
-Take out the test device from the foil pouch and place it horizontally.
-Suck the treated sample extraction from the assay buffer tube and place 3 drops into the sample hole â??Sâ?? of the test device.
-Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.
INTERPRETATION OF RESULTS
-Positive (+): The presence of both â??Câ?? line and zone â??Tâ?? line, no matter T line is clear or vague.
-Negative (-): Only clear C line appear. No T line.
-Invalid: No colored line appears in C zone. No matter if T line appears.
PRECAUTIONS
-All reagents must be at room temperature before running the assay.
-Do not remove test cassette from its pouch until immediately before use.
-Do not use the test beyond its expiration date.
-The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
-All specimens are of potential infection. It must be strictly treated according to the rules and regulations by local states.
LIMITATION
Canine Parvo Virus Antigen Rapid Test is for in vitro veterinary diagnosis use only. All result should be considered with other clinical information available with veterinarian. It is suggested to apply a further confirmative method when positive result was observed.
Dr. Guard is space sterilization and deodorant using pure chlorine dioxide.
[Dr. Guard]
* Sterilization test against COVID-19 showed a high result of 99.99% effectiveness
* Registered as a disinfectant for general disinfection in the Central Defense Countermeasures Headquarters of Korean government
* Corona 19 self-disinfecting environment approved product
* Completed safety check test and the only product certified by the Ministry of Environment
* Registered with the FDA. Safety verification completed in WHO.
* With proven technical skills, Dr. Guard has been recognized for its effectiveness in removing germs and odors.
* Obtained certifications from honorable global health institutions such as CE, FDA, PFDA and KEMENKES
[ClO2 Chlorine Dioxide]
* Chlorine Dioxide (ClO2) is a World Health Organization (WHO) recognized safety class A-1 safety material.
As a sanitary disinfectant already in Korea under the Drinking Water Management Act of 1999. It is soluble in chlorine dioxide. This is because there is no problem even when used for drinking water.
* The fatal drawback is that it is difficult to commercialize because it vaporizes quickly and is not easy to manufacture in gaseous form. However, since the sterilizing and deodorizing power is strong, manufacturers have added additional additives (sulfur, surfactant, etc.) for long-term storage.
* So, to make pure chlorine dioxide, special and difficult differentiated technology is required. Dr. Guard is a pure chlorine dioxide product made by a purely Korean technology by an honest company.
[Germs that can be sterilized by Dr. guard]
COROPNA-19 virus, N1N1, Pneumococcus, Dermatophyte, Norovirus, Pseudomonas aeruginosa, Fungi, Salmonella typhi, Staphyococcus aureus, Legionella
[Applications of Dr. Guard]
Using pure silicon dioxide chlorine sterilizing and deodorizing agent, we use the best technology in producing Dr. Guard for variety of purposes.
Bedroom, Bathroom, Refrigerator, Kitchen
No alcohol, No cancerous agents, No preservatives
Air purification, Antivirul action
[How to use Dr. Guard]
The stick contains main solution�?� and an ample (secondary solution)
1. Bend central part of the stick.
2. Once the ample inside the stick cracks, shake it enough to mix the power with the solution well.
3. As it turns yellow, the active ingredients are released to the surface of the stick.
4. After 3~4 weeks of usage, dispose stick into normal trash bag once solution inside turns transparent.
Strengths of antigen rapid test: FAST & EASY
(Compared with PCR test)
People could RAPIDLY & EASILY be tested as a prerequisite to school attendance, work, or travel.
FAST
--PCR test - the swab test looks for viral RNA - may take days to perform.
--Antigen test might take only 15-30 minutes to complete.
EASY
--PCR test swabs must be sent to laboratory to be performed by experienced technicians, it requires expensive and specialized equipment and can take days to get result.
-- Antigen test can be run in an office or at home in about 15-30 minutes. The sampling process is FAST & EASY and requires very little expertise. Similar tests are done routinely in clinics for influenza all the time.
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