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
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.
Sensitivity 25 miu
Features:
Precise design
Durable
Good quality
5090 Diagnostic Kits Suppliers
Short on time? Let Diagnostic Kits sellers contact you.
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.
We can provide Covid-19 Rapid Antigen Test. Test with reliable results within minutes. Made in the USA. Lateral flow assay, No equipment required, Results within 10 minutes, minimally invasive specimen collection, nasal swab, POC (in patient care setting). Detects SARS-CoV2 nucleocapsid protein antigen with ultra high performance. Identifies acute infection with 88.4% sensitivity and 100% specificity. Complies with FDA. Principals or Buyer's Mandates only. No broker chains. FOB or CIF. Minimum order 500000 test please.
