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.
The NeoPlexTM COVID-19 Detection Kit Assay is a real-time RT-PCR in vitro diagnostic test intended for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from respiratory specimens* obtained from individuals who meet COVID-19 clinical and/or epidemiological criteria. The NeoPlexTM COVID-19 Detection Kit is for use only under Emergency Use Authorization (EUA) in the US laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C.�§263a, to perform high complexity tests.
STANDARD M nCoV Real-Time Detection kit is used for rapid identification and detection of novel coronavirus (2019-nCoV) nucleic acids in human nasopharyngeal swabs and throat swab samples.
- One tube reaction for identification and detection of 2019-nCoV
- One-step Real-Time RT-PCR
- Provide all reagents required for PCR
- Designed according to WHO interim guidance for laboratory testing for 2019 novel coronavirus (2019-nCoV) in humans"
- nCoV primers/probes ORF1ab (RdRp) gene, E gene
- Provide Internal controls
- Test time : 90mins
- Specimen : Nasopharyngeal swab, Oropharyngeal swab, Sputum
- Applicable machine : CFX96. ABI7500
- CE, FDA EUA
Real-Time OneStep RT-PCR based assay system for detection of 2019-nCoV
CE-IVD
DiaPlexQâ?¢ Novel Coronavirus(2019-nCoV) Detection Kit is CE-IVD reagent. It is screening kit to detect Novel Corona Virus as 2019-nCoV from isolated total RNA. Basic principal of this kit is Real-time PCR method, which is able to detect specific target gene into total RNA. One step RT-PCR contents are progressively apply for one tube RT(Reverse Transcription) reaction and PCR amplification. You can monitoring the nucleic acid amplification result based on real time condition through the amplification plot. The Control Template (2019-nCoV) is provide as positive control to assist the clinical sample data comparison analysis.
- Detection target : 2019-nCoV ( COVID-19 )
- Target region : Orf1a, N gene
- Detection technology : Real-Time OneStep RT-qPCR
- Specimen type : Nasopharyngeal swab, Oropharyngeal swab, Sputum
- Compatible instruments : CFX96â?¢ Real-Time PCR System (Bio-Rad), ABI 7500 / 7500 Fast Real-Time PCR System (Applied Biosystems)
- PCR running time : ~ 120 mins
- Simple & Rapid detection system: OneStep Multiplex RT-qPCR based detection
- HotStart PCR: high-specificity
- Reliable system: automatic PCR control (not Internal control)
- Easy-to-use master mix: just adding template and Primer/Probe Mix
- Positive control included (Plasmid)
Our In-vitro Diagnostic product enables precise and efficient detection of the Coronavirus disease (2019-nCoV), utilizing Real-time RT LAMP PCR Real-time Reverse-Transcription Loop-mediated isothermal Amplification PCR method on nasopharyngeal swab specimen of a suspected patient.
- Detection target : 2019-nCoV ( COVID-19 )
- Target region : N gene
- Detection technology : Real-Time RT -LAMP PCR (with OneStep)
- Specimen type : Nasopharyngeal swab, Oropharyngeal swab, etc
- PCR running time : 20 mins
- Compatible PCR Device : CFX96TM Real-Time PCR System (Bio-Rad)
Key Characteristics
Rapid Detection System : Implementation of isothermal reaction method enables for 20-min test time
SYBR green Application : Fluorometric Detection enables for High Specificity
One step qRT-PCR system : en-bloc analysis without separate reverse-transcription process
User-Friendly Diagnostic System: Analysis possible only with the RNA specimen
Inclusion of Positive Control (Plasmid form)
iONEBIOs RT-LAMP PCR Kit is groundbreaking rapid and accurate; thus is the most competitive diagnostic kit for COVID-19 available in the global market.
933 Covid 19 Detection Kit Suppliers
Short on time? Let Covid 19 Detection Kit sellers contact you.
SARS-CoV-2 Antigen Detection Kit
For Nasal Swab, home testing
Colloidal Gold Method
Package Available: 1 Test/box, 5 Tests/box, 10 Tests/box, 20 Tests/box
Carton Size: 63 x 39 x39cm
Price is different based on QTY from 10K to 500K or above
Payment Term: T/T
Delivery time: 3-5 days
Price Valid: 30 days
Quality Warranty: 2 years.
We are supplying FDA's EUA approved Covid 19 Test Kit to the US.
Our COVID-19 Detection Kit is a real-time PCR based in-vitro diagnostic product intended for detection of the novel coronavirus
SARS-CoV-2 (COVID-19) RNA in sputum, bronchoalveolar lavage, oropharyngeal or nasopharyngeal smears collected from patients with
suspect viral infection
The kit is composed of Internal Positive Control (IPC), to monitor appropriate performance of amplification and detection of the kit.
Accurate detection of the viral RNA is confirmed parallelly by using Positive and Negative controls which are composed in the kit
I am representing SD Biosensor from South Korea that manufactures US FDA EUA approved Standard M nCo V Real-Time Detection Kit (COVID Testing kit). We have received US FDA EUA approval to export Covid 19 detection kit in April and can directly export from Korea.
SD Biosensor is one of the few companies that has received US FDA approvals and have already sold 1.5 million testing units to US government (Based on US government reaching out to South Korea Government for help with procuring Covid Testing kits).
I'm currently in Seoul, South Korea but I'm a US citizen helping SD Biosensor as an agent to help buyers procure these testing kits. This company has capability to manufacture over 600,000 testing units a day and have enough supplies readily available for an immediate export.
Please email me at Jinsoo.park@yahoo.com to receive US FDA EUA Approval and product information. rapid test kits which are not FDA approved are in the low to mid $20 range and the price for FDA EUA approved standard test kits are around high $20s to low $30s and depending on the contract length and quantity we have some room for negotiation. Also these kits have to be refrigerated shipped so there will be some additional cost for this.
The Rapid COVID-19 Antigen Oral Fluid Self-Test is a lateral flow test for the qualitative detection of nucleocapsid protein antigenfrom SARS-CoV-2 in oral fluid from individuals who are both symptomatic and asymptomatic.This testis intended to aid in the rapid diagnosis of Coronavirus infections. If symptoms persist despite negative test results it isrecommended to visit a healthcare professional to seek follow up care.Rapid COVID-19Antigen Oral Fluid Self-Test is intended foruse by layperson home users.
Corona Antigen Tests, single packed
On Stock in
700 000 units immediately
up to 1,2 million on the way and roll-over orders in line with producer
without engagement, subject to prior sale
We are manufacturer and supplier of high quality molecular diagnostics product among covid 19 detection kits consisting of:
1]. covid 19/sars cov 2 nucleic acid test kits to detect the covid 19 standard, uk and south africa variants (rt pcr).
2]. covid 19/sars cov 2 antigen rapid test kits.
3]. covid 19/sars cov 2 antibody (igg/igm) rapid test kits.
in addition to a product of quality, we offer very competitive price and we have high production capacities to assure a continuous supply of product without shortage..Manufacture, oem
