1. Nasopharynx swab specimen, non-invasive 2. Very simple to use 3. Convenient, no devices required 4. Rapid, results within 20 minutes 5. Cost-efficient 6:Listed on German BfArm ,got approval by PEI Clinical report from local CDC Sensitivity is 97.14%, Specificity is 100%, total accuracy rate is 99.68%.
The product is based on the principle of antigen-antibody reaction and immunoassay technique. The test device contains colloidal gold labeled SARS-CoV-2 recombinant protein, mouse-anti human IgG antibody immobilized in G test area, mouse-anti human IgM antibody immobilized in M test area and the corresponding antibody in quality control area (C). During the test, when the SARS-CoV-2 IgM antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgM antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. The conjugates migrate upward through capillary effect and would be captured by mouse-anti human IgM antibody immobilized in M test area subsequently and this produces a purple-red band appears in the M test area. When the SARS-CoV-2 IgG antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgG antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. Theconjugates migrate upward through capillary effect and would be captured by mouse-anti human IgG antibody immobilized in G test area subsequently and this produces a purple-red band appears in the G test area. If it is a negative sample, there is not a purple-red band appeared in the M and G test area. Regardless of the presence or absence of the SARS-CoV-2 antibody in the sample, a purple-red band will appear in the quality control area (C). The purple-red band in the quality control area (C) is a criterion for judging whether there is enough sample and whether the chromatography process is normal. It also serves as the internal control standard for reagents.
KOSTEC can supply Korean rapid test kits, which are not only faster and easier in test but alsoprovide accurater test results. Also price is very much attractive! If you have any interest in this test kits, do not hesitate to contact me. Thanks!
* NEW* Covid-19 ANTIGEN RAPID TEST KIT *NEW * with CE Mark EU APPROVED | Collodial Gold Method | 15 Minutes Rapid Covid-19 Rapid Antigen Test Kit | Collodial Gold Method Accurate: 96.1% sensitivity, 96.67% specificity compared with PCR FAST: only 15 minutes required EASY-TO-USE: no special requirements Room temperature storage MOQ 2000 units (25pcs) per unit MAX 300.000 units PER DAY Payment terms 100% TT in Advance Lead time 7 days Global delivery Results
Aflatoxin b1 rapid test for detecting aflatoxin b1 in feed. Cut-off, 20ppb Assay time: 5min Advantages: 1. No complex equipment used in the assay. 2. Farmers can use the test easily 3. Very fit for in field rapid detection 4. Whole procedure for detect a sample is no more than 10min 10 tests/kit
Hello, I have FDA approved rapid COVID 19 testing kit. Price 6$, all the certificates and the documents are Available
Canine brucella ab rapid test is a lateral flow immunoassay for quick detection of brucella canis in serum. Welcome your enquiry! Specifications Specimens: serum Shelf life: 18 months Storage temperature: room temperature(2-30c degree) 10 tests per kit, sealed in foil pouch
Hello all, Greetings from Dermaqual. Dermaqual is a Reputed French Biomedical Laboratory since 2003. We produced the world-first Coronavirus COVID-19 Rapid Test Kit "Sanitized" its based in IgG/IgG antibody. Its US FDA, CE & ISO Certified. The test kit will take only 10-15 min. to show if you are infected. We are looking for Distributors in EMEA region. If interested please send us an email at contact us.
Our COVID-19 rapid test kit can be used effectively on many levels for proper screening and strategic preparedness toward the pandemic. The test kit requires no sophisticated equipment nor laboratory settings. Our SARS-COV-2 Antibody Rapid Test Kit can be applied for screening of COVID-19 disease on the following: General practitioners and external clinics level to detect previous SARS-COV-2 viral infections on both symptomatic and asymptomatic patients. Determination of the immunity level of front-line healthcare workers, which can help in the development of pandemic preparedness strategies at national levels. Epidemiological COVID-19 surveys at national and district levels for research purposes. Airport screening for arriving /departing passengers to control the pandemic in the aviation industry. Suspected cases exclusion to minimize cost and time spent in the RT-PCR testing procedures. Screening on the national level to facilitate decision making regarding lockdown and curfew easing strategies. Phoenix Bioscience is offering a competitive price for a high-quality kit that is made in Canada and used currently to combat the pandemic in most American cities.
Singclean Covid - 19 lgG lgM Rapid Test Kit - Colloidal Method
Intended Use Package Storage Specimen Type Shelf life Time to result Detection of SARS-CoV2 antigen 20 Tests / kit 1 - 40 Nasopharynx / Nasopharyngeal 24 months from manufacture date 5 - 8 minutes
Product Name Neutrophil Gelatinase-Associated Lipid Carrier Protein (NGAL)Test Kit (Immunofluorescence Chromatography) Purpose To detect the NGAL in human plasma/serum/whole blood in vitro quantitatively.For Professional Use only. Principles of Detection The NGAL Test is a fluorescent lateral flow immunoassay. The test consists of: 1) a conjugate pad containing NGAL antibody conjugated with fluorescent microspheres and a control antibody (goat anti-chicken IgY antibody) conjugated with fluorescence microspheres, 2) a nitrocellulose membrane strip containing a test line (T line) and a control line (C line). The T line is pre-coated with anotherNGAL antibody, and the C line is pre-coated with a control line antibody (chicken IgY antibody). NGAL concentration in specimen is positively correlated with the fluorescent density of the microspheres, after the measure and calculation of the quantitative fluorescence immunoassay analyzer, then the analyzer would calculate the concentration of NGAL according to the preset calibration curve in the machine and display the result, detection unit is ng/mL. C line should appear in any cases, which indicates the reaction system is effective. Reference range Reference value: 37-180ng/mL; The reference value is verified by referring to similar products on the market. Due to ethnic and regional differences, each laboratory can establish its own reference interval according to the actual situation.
1) Zhenrui (Immediate Stock) at HKD65 per test 2) Newgene (available in 3-5 days upon order) at HKD30 per test 3) Aripa (available on 22 Feb 2022) at HKD68 per test 4) Healgen (available in 1-2 weeks) at HKD48 per test 5) Giant King (available in 1-2 weeks) at HKD48 per test 6) BioTeke (immediate available - 1M) at HKD30 per test 7) TBG (MOQ : 1M) at USD4.50 per test
Antigen Detection Rapid Lateral Flow Test (latex bead-based) AIVD Biotech's Ag test is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein (NP) antigen in direct nasal swabs from individuals suspected of infection. Description: This kit utilizes the principle of latex bead immunochromatography to qualitatively detect the Np antigen in human nasal swabs. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of suspected patients. The test contains latex bead conjugate pad and a membrane strip pre-coated with antibodies specific to the antigen on the test lines (T). If novel NP 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 anti- 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. Storage conditions 1. Store at the dark place, room temperature 18~28C with low humidity. 2. After opening the foil bag, please use the test cassette within 30 mins. 3. Expiration period 12 month 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 2~8C for up to 4 hours prior to testing. Performance Characteristics A total of 365 samples from suspected patients were tested by the RT-qPCR test. Testing results are shown in the following table: PCR AIVD Antigen Rapid Test Kit Positive Negative Positive 59 8 Negative 6 292 Total: 65 300 Sensitivity: 90.7%; Specificity: 97.3%.
500k Landed in NY weekly. Connected to second largest Sienna distributor in North America. Carton Pricing starts at $4.50. Message for Pallet and up pricing. PO-POL-Invoice-Wire-Ship/Pick Up
Our products are directly from factories, Boson, H-Guard, Flow flex, etc.
Products we have access to for the US Market OTC: iHealth 2 pack - 4-7 business days from payment AccessBio 2 pack - Available within 3-5 business days FlowFlex 1 Pack- Available for delivery after the 7th Feb Roch 5 Pack- 5 day lead time from payment SD-Biosensor 1 or 2 pack: 100,000 available daily CIF/DDP from South Korea On/Go: Weekly allocation is available on-going, Made in USA! POC: Sienna Celltrion Indicaid GenBody Spring Health OTG: ICPO x Invoice x Inspect and Pay products are available for spot purchases, at a premium price. OTG or OTW: Wire and Ship products are sold with CHAIN OF CUSTODY, AWB, BOL or other proof of Allocation... at slightly better rates. Production opportunities, on-going Allocation, or larger volumes are sold at the best price, with tiered pricing for longer duration contracts. There are financing opportunities available: Factoring ICPO x CounterSigned Invoice for Gov POs, Hospital Organizations, and Fortune 500 Companies. Everyone else must Fund Escrow, or Block Funds, with explicit verbiage guaranteeing the release once the order reaches America, clears customs, and is available for physical inspection/ delivery to the clients destination.
iHealth Tiered Pricing - PrePay or Financed 1M MOQ, 10M & >20M Aggregate Option 1- PRE-Pay & Ship PO x Invoice x Wire 100% x Ship DDP [Better Price, Money Up-front] $14, $13, $12 [.25 comms included] Option 2- Blue Chip Financed Deal ICPO x Invoice w/ POF x Countersign Invoice w/ Commitment to Release Upon Delivery [Requires Strong Buyer KYC] Option 3- Funded Escrow ICPO x Invoice x Fund Escrow/ Block Funds x Inspect & Release [Creates Security - Inspect & Pay] PO details: Ruben L Hudson Advanced Healthcare Resources LLC c/o STM Bio - Goldmanifestor Financed options - Total contract value - 1M would be 14.50 base 10M would 13.50 base 20M+ would be 12.50 base [.25 comms included]
Antigen tests are used in the diagnosis of respiratory pathogens and are immunoassays that detect the presence of a specific viral antigen, which implies current viral infection. COVID-19 Antigen Rapid Test is designed to detect the presence of viral proteins (antigens) expressed by the COVID-19 virus in a sample from the respiratory tract of a person and is gives results in a few minutes whether someone is infectious. Approved by clinical specimens and authorities, this product is intended exclusively for professional use in the laboratory and at the point-of-care. .
Our Panodyne Sars-CoV-2 Antigen rapid swab test kits offers a quick and efficient solution for the early detection of COVID-19 infection within both symptomatic and asymptomatic individuals. Uses a specially designed swab to take samples from either the nasal cavity or tonsils to reveal if a person is infected or not. Suitable for mass testing and for screening workforce in business settings.
