Description Foot-and-mouth disease virus (FMDV) causes an acute vesicular disease of cloven-hoofed animals and continues to be a threat to livestock worldwide with outbreaks causing severe economic losses. RIDX FMDV 3Diff/PAN Ag Combo Test Kit is a lateral flow chromatographic immunoassay for the qualitative detections of all 7 serotypes antigens of FMDV in bovine or porcine samples. 3Diff Ag Test: FMDV 3Diff detects FMDV Asia1, type A, and type O antigens. Three test lines (AS, A, O) and the control (C) line on the surface of the device. PAN Ag Test: FMDV PAN detects all 7 serotypes (type O, type A, type C, Asia1, SAT1, SAT2, and SAT3) of FMDV antigens. The test line (PAN) and the control (C) line on the surface of the device. If the FMDV antigens exist in the sample, that bind to the gold-conjugated FMDV antibodies. The complexes move through the membrane by capillary force and respond to the FMDV antibodies on the test line, resulting in a red line. The control line indicates that the test is performed correctly. The highly selective and sensitive four monoclonal antibodies to FMDV are used as capture and detector in RIDX�® FMDV 3Diff/PAN Ag Combo Test Kit. These antibodies are capable of detecting FMDV antigens in bovine and porcine samples with high accuracy. Specimen Bovine or porcine saliva, tissue or vesicular fluid around lip, tongue, gums, nose, or hoof Components FMDV 3Diff/PAN Ag combo test device (10 tests) Disposable swab (10 ea) Sample dilution buffer (1 vial) Disposable dropper (10 ea) Sample tube (10 ea) Features Clinical Sensitivity 1. Type O 88.2% (n=60/68) vs. PCR 2. Type A 100% (n=70), Asia1 100% (n=62), SAT1 100% (n=20), SAT2 100% (n=20), SAT3 100% (n=20), C 100% (n=20), in spiking samples with virus (titer: 1.0x105 TCID50/ml or higher) Clinical Specificity 1. Type O, type A and PAN: Bovine 100% (n=92), Swine 100% (n=400) 2. Type Asia1: Bovine 100% (n=92), Swine 99.5% (n=398/400) Differential diagnosis of 3 different serotypes (O, A, Asia1) of FMDV Concurrent diagnosis both of viral common antigens (all 7 serotypes) and serotype-specific antigens (O, A, Asia1) Packages 10 Tests/Kit 12 Kits/Box (120 Tests/Box) or 40 Kits/Box (400 Tests/Box)
This is Product is very demand due to pandamic situation. We are supplying ICMR approved ,CE certified product
We are supplier of ICMR approved ,CE certified test kits for Dengue and Malaria with international standard
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: 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
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
Minimum order - 5000 units Port - Shanghai, Ningbo Payment - T/T, L/C 25 pieces * One step test for the Novel Corona-virus (COVID19) (2019nCov) lg
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.
Product name:FIV Ab/FeLV Ag Combo Rapid Test Kit MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification:Â ISO9001 Packing: 10pcs/box
Product name:Canine Heartworm Antigen Rapid Test (CHW Ag) MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification:Â ISO9001 Packing: 10pcs/box
Product name:CPV Ag+CCV Ag+Giardia Ag Combo Rapid TestC MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification:Â ISO9001 Packing:Â 10pcs/box
Product name:Canine Pregnancy@Relaxin Rapid Test (Relaxin) MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification:Â ISO9001 Packing: 10pcs/box
Product name:Giardia Antigen Rapid Test (Giardia Ag) MOQ: 1PCS Use: Vet Diagnosis Assay Time:Â 5 - 10 minutes Shelf life:Â 18-24 Months Specimen: Serum Plasma Feces, vomit Sensitivity: 99.8% Storage:Â 2-30 Degree Certification: ISO9001 Packing:Â 10pcs/box
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. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY 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. REAGENTS AND MATERIALS -Test devices, with disposable droppers -Assay buffer -Cotton swabs -Products Manual STORAGE AND STABILITY 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.
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.
Rapid Antibody kit used for testing to detect the neutralized Antibodies in Patrons.
Covid19 Antigen testing kit is used for test patrons on Covid19 symptoms.
For in vitro qualitative detection of SARS-CoV-2 nucleocapsid antigen in nasal (NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days after onset of symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, not for at-home testing. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, or 2019-nCoV) is an enveloped non-segmented positive-sense RNA virus. It is the cause of coronavirus disease (COVID-19), which is contagious in humans. SARS-CoV-2 has several structural proteins including spike (S), envelope (E), membrane (M), and nucleocapsid (N). The antigen is generally detectable in upper respiratory samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but the clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out a bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Negative results should be treated as presumptive, which do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient's recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. For in vitro diagnostic use only. For professional use only .
