SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold Immunochromatography) Product Description SARS-COV2 Antigen Rapid Test Card contains a gold-labeled novel coronavirus N protein monoclonal antibody pre-coated on the bonding pad and a paired novel coronavirus N protein monoclonal antibodies �xed in the test line (T) and corresponding antibodies in the quality control line (C). SARS-COV2 Antigen Rapid Test Kit can detect the virus from the rst phase of infection (2-3 days before potential symptom onset) to the last phase of infection (7-10 days after potential symptom onset). Used to test COVID-19 antigen Card-like format detects the nucleocapsid (N) protein of the virus. Gold-labelled SARS-CoV-2 N protein monoclonal antibodies immobilized on the test area, with corresponding antibodies in the quality control area. Swabbed specimens from the nasopharynx or oropharyngeal, result in 15 minutes Product Features Non-invasive Simple to use Convenient, no devices required Rapid, get a result in 15 minutes Stable, with high accuracy Inexpensive, cost-efficiency Related News On 26th Jan 2021, report from PEI of an official test that The Federal Institute for Drugs and Medical Devices (Bundesinstitut fr Arzneimittel und Medizinprodukte, BfArM) authorized to perform, declared that Lepu Medical SARS-CoV-2 Antigen Rapid Test Kit has fulfilled all the minimum criteria for antigen tests conducted by PEI in consultation with the Robert Koch-Institut (RKI). In March 2021, German BfArM approved Lepu Medical SARS-CoV-2 antigen rapid test kit for home use. The test kit makes the coronavirus detection procedures rapid and easy.
his kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Tylosin (TYL) in the sample such as poultry tissue, honey. Specification 96wells per kit
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Aflatoxin B1 (AFB1) in the sample such as grains and feed.
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Nitroimidazoles (NMZ) in the sample such as tissue, honey and eggs.
This kit adopts the method of indirect competitive enzyme-linked immunoassay (ELISA) to detect Tetracyclines (TCs) in the sample such as tissue, honey and eggs. Technique Data Kit Sensitivity: 0.05ppb (ng/mL) Reactive Mode: 37�ºC, 30min~30min~15min Detection Limits: Sample Detection Limits Tissue, liver, eggs 2ppb Honey 2ppb Urine 0.5ppb Milk 2ppb Milk powder 4ppb Cross-reaction rate: Tetracyclines..................â?¦.....100% Oxytetracycline ...............â?¦...107% Chlorotetracycline..................16.7% Doxycycline ..................â?¦.......4.2% Sample Recovery rate: Sample Recovery rate Tissue, liver, egg 75�±20% Honey 80�±20% Urine 80�±20% Milk, Milk powder 75�±20% Our products related to Bovine disease detection mainly include the following Zearalenone (ZON/ZEN) ELISA Kit Aflatoxin B1 (AFB1) ELISA Kit Deoxynivalenol � (DON) ELISA Kit Aflatoxin M1 (AFM1) ELISA Kit Total Aflatoxin � (AFT) ELISA Kit T2 Toxin (T2) ELISA Kit Fumonisin B1 � (FB1) ELISA Kit Ochratoxin A (OTA) ELISA Kit Shenzhen Finder Biotech Co., Ltd. is a a high-tech enterprise located in Shenzhen, China. Our company is engaged in rapid detection of food safety (such as residue detection of veterinary drugs, additives, hormones, mycotoxins), rapid diagnosis of animal diseases and related product development. There are hundreds of products. Secondly, the diagnostic kits and test cards for animal diseases mainly for livestock and poultry have been widely used in Animal Husbandry Government Department, scientific research institutions and universities, which provides a strong basis and guarantee for monitoring immunity and diagnosis.
New Arrival Pass Management Kiosk for Temperature Measurement & Face Recognition, Specially designed for COVID-19/Coronavirus. Introduction ONT-SV-1081D, pass management vertical module of temperature measurement & face recognition uses Rockchip RK3288 / RK3399 / Qualcomm MSM8953 high-performance hardware platform, equipped with industrial-class binocular camera, live face recognition technology and infrared thermal imaging module to support face-with-mask identify. It also supports expansion of various peripherals such as ID card readers, fingerprint readers, etc., which can be applied to gate passages and attendance system to achieve safe and efficient access control for personnel. Features 1. 8-inch IPS full-view LCD display. 2. Industrial-class appearance, waterproof and dustproof design which is stable and reliable. 3. Supports 30,000 face database. The 1: 1 comparison recognition rate is more than 99.7%, the 1: N comparison recognition rate is more than 96.7%@0.1% misrecognition rate, and the live detection accuracy rate is 98.3%@1% misrejection rate. Face recognition pass speed is less than 1 second. 4. Supports accurate face recognition and comparison while wearing a mask. 5. Using industrial-grade binocular wide dynamic camera, night infrared and LED dual photo flood lamp. 6. Support processors with strong performance: Rockchip RK3288 quad-core processor, Rockchip RK3399 six-core processor and Qualcomm MSM8953 octa-core processor. 7. Supports human body temperature detection and temperature display. The best temperature detection distance is 0.5 meters. The longest distance at which body temperature can be measured is 1 meter. The measurement error is plus or minus 0.5 â??. 8. It only takes a few seconds for detection, and supports automatic alarm for body temperature abnormality. 9. Attendance temperature measurement data is exported in real time. 10. Supports various peripheral expansions such as ID card reader, fingerprint reader, IC card reader, two-dimensional code reader, etc. 11. The documentation is complete and supports secondary development. 12. Support system level, APP offline level, APP + background network level multiple API docking.
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Elisa Kit.
HIV Antigen/antibody for ELISA recombinant antigen HIV-1 gp41+gp120 HIV-1 gp41 HIV-2 gp36 HIV-1+2 gp41+gp120+gp36 HIV-1 P24 HIV-1 gp41+gp120-HRP conjugate HIV-2 gp36-HRP conjugate antibody Monoclonal Anti-HIV P24 Polyclonal Anti-HIV P24 Biotin HIV Antigen/antibody for Rapid test recombinant antigen HIV-1 gp41+120 HIV-2 gp36 HIV-1+2 gp41+36+120 antibody Monoclonal Anti-HIV P24 Polyclonal Anti-HIV P24 Fapon Biotech provide gene engineering recombinant antigens and antibodys of HIV type 1¿¬¿«2 and group O, which can be used in ELISA and Rapid Test Kit, with high sensitive specific and stability.
HCV recombinant antigen for ELISA HCV NS3 HCV Core HCV Coreú½NS3+NS4+NS5 HCV Coreú½NS3+NS4+NS5ú¡HRP Conjugate for Rapid test HCV Core+NS3+NS4+NS5 (IgG indirect) HCV Core+NS3+NS4+NS5 (for coating, Sandwich) HCV Core+NS3+NS4+NS5 (for conjugating, Sandwich) Fapon Biotech provide gene engineering recombinant antigens of HCV, which can be used in ELISA, Rapid Test Kit and research, with high sensitive specific and stability.
Covid 19 products, vtm, nucleic acid detection kit, nucleic acid extraction kit, the nucleic acid isolation system, quantitative real time pcr system, sars cov 2 nucleic acid detection kit, rapid test antigen kit, igg/igm antibody kit.Transportation and shipping
Covid 19 antigen rapid test kit.
Antigen tests, nasopharyngeal swabs, oral swabs, vtm/ utm kits, saliva kits, etc..
COVID test kit.
Animal disease (veterinary )diagnostics elisa kit ,colloidal gold rapid test kit and pcr tests, (swine/poultry/pet/ruminants) food safety elisa test kit & colloidal gold rapid test kit (), human ivd and medical equipments, analyzer.Oem solution or distributorship
Intended use: AIVD COVID-19(SARS-CoV-2) IgG/IgM Rapid Test is a single use, rapid device for qualitative detection of total antibodies against 2019 novel coronavirus (SARS-CoV-2) in human serum, plasma or whole blood specimens. The kit is intended for screening of patients suspected for infection with SARS-CoV-2, and as an aid in the diagnosis of the coronavirus disease 2019 (COVID-19). Descriptionï¼? Novel coronavirus pneumonia (NCP) or SARS-COV-2, that was officially named by the WHO as â??Corona virus disease 2019â?? (COVID-19), is a respiratory infection caused by a new virus that was first identified in late 2019. IgM/IgG Rapid Kit can specifically detect IgM and IgG antibodies of COVID-19, covering the entire course of infection and recovery period of patients. This approach improves the overall diagnosis of COVID-19 in both acute and recovery phases of illness. This kit utilizes the principle of colloidal gold immunochromatography to qualitatively detect the new coronavirus (COVID-19) IgG / IgM antibodies in human serum and plasma. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of COVID-19 suspected patients. This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well, and then add the required amount of a diluent. The IgG / IgM antibodies in the sample will interact with the colloidal gold-labeled COVID-19 recombinant antigen on the conjugate pad. Then the conjugate pad will release re-solubilized conjugate onto the nitrocellulose membrane. The nitrocellulose membrane (NC membrane) diffuses it forward. As the sample moves along the device binding reagents situated on the nitrocellulose membrane bind to the target at the test line. If the sample contains a COVID-19 IgG antibodies, they will bind to the colloidal gold-labeled novel coronavirus recombinant antigen, diffuse forward, and then react with the anti-human IgG antibodies immobilized on the NC membrane detection line (T2 line). Similarly, if the specimen contains IgM antibodies to COVID-19, the antibodies will react with antigen-coated particles, the conjugate migrate laterally forward, and cause a colored line (T1 line). The darker the color of colloidal gold on the test line, the higher the concentration antibodies to COVID-19 in the sample. Accuracy:ï¼?> 90% Specificity: 97% Basic Protocolï¼? 1. Remove the test specimen, required reagents from storage conditions, and equilibrate to room temperature. 2. Unpack the aluminum foil bag, place the test horizontally on the table and number it. 3. Add 10ul serum, plasma or whole blood sample to the sample well with a pipette or a dropper. Slowly add 2 drops of sample dilution (about 60uL) to the sample well. 4. Read the results within 10-15 minutes after adding the sample, and the results will be invalid after 30 minutes.
Description This kit utilizes fluorescence quantitative probe-based PCR and guarantees a high specificity to ensure accurate one-step identification of ORF1ab and N genes of 2019-nCoV. The kit offers a highly sensitive test with a limit of detection as low as 500 copies/ml. The results are available within 1.5 hour. Kit Contents (48 Tests /Kit) Dual Enzyme solution A 50 µl Dual Ncvo-O / N reaction solution A 1 ml Dual Ncvo-O / N positive control A 200 µl Dual Negative control A 200µl Applicable equipment ABI series, Bio-Rad, Roche series and other fluorescent real-time PCR instruments. Specimens requirements Specimen type: nasopharyngeal swab from suspected infection; virus cell culture fluid, etc. Basic Protocol 1. Sample preparation. Take the test sample and extract the RNA nucleic acid according to the instructions of the nucleic acid extraction kit. The nucleic acid extraction product should be stored at -20 C. 2. Reaction mixture preparation According to the total number of test samples, the number of PCR reaction tubes needed is. N = number of samples + 1 negative control + 1 positive control. The following protocol is recommended for a 20 µl reaction volume. If the volume of reaction changes, please adjust proportionally. Components Volume Dual Enzyme solution A 1 µl Dual Ncvo-O / N reaction solution A 19µl Final Volume: 20 µl 3. Sample adding. Add 5 µl each of the extracted RNA, positive and of negative control to corresponding reaction tubes. After assembling all the components, cover the tube caps and gently mix the contents of the tube, mix well, and centrifuge briefly. 4. Perform quantitative PCR Place the reaction tube inside a real-time PCR instrument. Set the channel and sample information, reaction system volume 25 µl. Select the following channels: FAM channel for nCOV-ORF1ab, VIC channel for nCOV-N. Perform quantitative PCR using recommended cycling parameters settings: Step Temperature Time Number of cycles Fluorescence Detector 1 50C 15 min 1 Off 2 95C 3 min 1 Off 3 95C 10sec 45 Off 60C 30 sec On Result analysis: 1) Set the baseline: Generally, it is set to 6-15cycle for ABI 7500, 7700 and other instruments, 3-15cycle for PE5700, and 6-12cycle for MJ Research Option2. Under special circumstances, the baseline can be adjusted accordantly. 2) Set the threshold: The threshold line just exceeds the highest point of the negative control amplification curve (random noise line).
AIVD Biotechs COVID-19 Ag test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein (NP) antigen from SARS-CoV-2 in direct nasal swabs from individuals suspected of COVID-19. Description This kit utilizes the principle of latex bead immunochromatography to qualitatively detect the new coronavirus (COVID-19) Np antigen in human nasal swabs. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of COVID-19 suspected patients. The test contains latex bead conjugate pad and a membrane strip pre-coated with antibodies specific to SARS-CoV-2 antigen on the test lines (T). If SARS-CoV-2 antigen is present in the specimen, a visible band appears on the test lines (T) as antibody-antigen-antibody latex bead complex forms. The control line (C) is used for procedural control and should always appear if the test is performed correctly. This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well. If sample contains the antigen, it will interact with the latex bead-labeled COVID-19 anti-SARS-COV-2 NP antibodies on the conjugate pad. Required components 1. A foil pouch with a desiccant and a single-use test card, 1 piece 3. Sterile swab, 1 piece 3. Extraction buffer tube (1 ml), 1 tube. 4. Instructions for use, 1 piece. Specimen requirements: 1. Nasopharyngeal swab specimen. 2.Specimen should be tested as soon as possible upon collection. If the sample has to be stored, store the swab sample at room temperature for up to 1 hour or 2~8â?? for up to 4 hours prior to testing. Specimen preparation 1. Insert the extraction buffer tube into the tube rack, make sure that the sample tube is firmly upright and touches the bottom of the rack. 2. Insert the swab into an extraction buffer tube. 3. Gently stir the swab in the tube, and then left swab inside the tube for 1 minute or Mix on the vortex mixer for about 30 seconds, 4. The sample should be tested immediately after collection. If it cannot be tested in time, it should be stored in the virus transport matrix. The specimens can be stored at 2-8C for 4 hours Basic Protocol Step 1: If the sample is refrigerated, remove the sample to be tested and the required reagents from the storage conditions, equilibrate to room temperature (15~30C) Step 2: When preparing to test, open the aluminum foil bag, take out the test card, and lay it flat on a table. Step 3: Mark the sample number on the test card, Step 4: Using pipette add 50ul of the sample into a sample well on the device, Step 5: Read the result within 15 minutes, Please read the result after 15 minutes. After observing and recording the result, please discard the test card to avoid affecting the result judgment. Do not read test results after 30 minutes. It may give false results.
Viral transport medium(vtm) includes non inactivated disposable virus sampling tube(non inactivated vtm) and inactivated isposable virus sampling tube(inactivated vtm), nucleic acid extraction reagent kit(rna dna extraction reagent kit) includes nucleic acid extraction reagent kit 64t(auto) and nucleic acid extraction reagent kit 96t(auto), nucleic acid extractor(nucleic acid extraction system) includes automatic nucleic acid extractor with model no.nfast 32a and nfast 96, pcr test reagent kit includes rt pcr test reagent kit and freeze dried rt pcr test reagent kit, pcr system(pcr instrument) we have ma 6000 fluorescence quantification real time pcr system, ma 1630q fluorescence quantification real time pcr system, etc..
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