Product Details:
Number of Reactions(Preps)/Kit ; 2
Brand ; iHEALTH
Test Method : Antigen Test
Result Time (Rapid Kits) : 15mins
Sample Type : Nasal Swab
Cat. No : ICO-3000
iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
Number of Reactions(Preps)/Kit 30T
Brand CTK BioTech
ICMR Approved Yes
Result Time (Rapid Kits) 20min
CAT No : AR5001C
Details :
Utilizes Recombinant Orientia tsutsugamushi antigens.
Qualitative detection and differentiation of antibodies(IgG and IgM) against Orientia tsutsugamushi (Scrub typhus)
Compatible with Whole blood, Serum and Plasma.
Sensitivity: For IgG 95.4% and IgM 96.1%, Specificity: For IgG 96.8% and IgM 97.6%.
Results in 20 minutes.
Each kit contains:
Individually sealed foil pouches containing:
One cassette device
One desiccant
Detection buffer (tris-based buffered solution with preservatives)
Instructions for Use
FlowFlex Sars-CoV-2 Antigen Rapid Test Self Test - Single Pack
The Flowflex SARS-CoV-2 Antigen Rapid Lateral FlowTest is a lateral flow chromatographic immunoassay for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimens directly from individuals who are suspected of an active COVID-19 infection by their healthcare provider within the first seven days of the onset of symptoms.
Supplied in a single pack
Cassette Format
Detects the nucleocapsid protein antigen from SARS-CoV-2
Nasal Specimen sample. Anterior Nares Only Test (2-4cm inside the nostril)
Results in 15 minutes
CE Marked for Self Test
Used by NHS track and trace as home test
Unique ID QR code number on each cassette
Pack Contents
1 x Test Cassette with QR code and unique ID number
1 x Extraction Buffer Tube
1 x Disposable Swab
1 x Waste Bag
1 x Package Insert
Features:
Fully Home Use Approved
FDA Approved
Validation from Public Health England Porton Down.
Full Home Test Approval Granted in the UK & EU
Registered with MHRA and CE Marked.
Used and trusted by companies around the world including all UK airports and the NHS.
Cat No : 195000. TheBinaxNOWTM COVID-19 Ag Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swabs from individuals suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.
Cat. No : COVAG025-1.The GenBody COVID-19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) oranteriornasal (AN) swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first six days of symptom onset.
1752 Rapid Test Kits Suppliers
Short on time? Let Rapid Test Kits sellers contact you.
Cat No : A28523. TaqPath 1-Step Multiplex Master Mix (No ROX) is a fast, single-tube, 4X RT-qPCR mix that provides for sensitive, reproducible detection of up to four different RNA/DNA targets in a single multiplex reaction. Particularly useful for diagnostics, virus detection, and high throughput gene expression workflows, the mix includes thermostable MMLV reverse transcriptase, dNTPs, UNG, and thermostable Fast DNA polymerase all in a single tube. TaqPath is manufactured under a strong ISO13485 quality management system and is designed to produce consistent product performance lot after lot.
This single-tube, 4X format facilitates easy reaction set upâ??just add user-supplied assay and sample (Figure 1). With reproducible performance even in the presence of inhibitors, coupled with stringent quality control to minimize lot-to-lot variation, TaqPath 1-Step Multiplex Master Mix (No ROX) is a superior choice for your multiplex diagnostic testing or development needs.
High sensitivity
To enable reproducible detection of low-titer pathogen and transcripts, TaqPath 1-Step Multiplex Master Mix (No ROX) has been optimized as a higher-concentration 4X master mix that allows you to input more sample into each reaction, increasing sensitivity even in low-volume reactions. Figure 1 shows the consistency of results obtained when detecting 10 copy inputs of RNA target.
Cat. No : ICO-3000. iHealth COVID-19 Antigen Rapid Test is the simplest way to detect SARS-CoV-2 nucleocapsid protein antigen. It only takes 4 steps and 15 minutes to complete the test. The test is also non-invasive. You won't need to collect a sample from deep in your nasal cavity to get accurate results.
CAT No : Q-NCOV-01G. STANDARD Q COVID-19 Antigen Test kit is chromatographic immunoassay for the qualitative detection of SARS CoV 2 nucleocapsid antigen present in human nasal sample.
PocRoc SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) is intended for qualitative
detection of SARS-CoV-2 nucleocapsid antigen from NS specimen or VTM sample
without guanidine
The 2019-nCoV Ag Saliva Rapid Test is a lateral flow immunoassav intended for the qualitative detection of nucleocapsid protein antigen from2019-nCoV in saliva specimens directly collected from individuals who are suspected of COVID-19 by their healthcare provider within the first 7 days of symptom onset
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.
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 .
Lateral flow assay
No equipment required
Rapid results within 10 minutes
Minimally invasive specimen collection (nasopharyngeal swabs)
POC setting (i.e. in patient care settings) by medical professionals
Detects SARS-CoV-2 nucleocapsid protein antigen with ultra high performance
Identify acute infection wit 88.4% sensitive and 100% specificity
20 test/box
20 test devices
20 assay buffer
20 extraction vials and caps
20 specifimen collection swabs
1 positive and 1 negative control swabs
1 instructions for use
RAPID TEST IgG/IgM - EMERGENCY RESPONSE KIT FROM THE UNITED STATES!
The COVID-19 Rapid Test for Screening, Diagnosis, and Monitoring is a lateral flow immunoassay, a way to qualitatively assess the presence of IgG and IgM antibodies specific for SARS-CoV-2 from a person sample
Product advantages
COUNTRY OF ORIGIN
The United States
EARLY DISCOVERY
Individual test avoids cross-infection
WHOLE SPECTRUM
The cover early, mid and late phase of the disease
FAST RESULTS
10 minutes
HIGH ACCURACY
98,43%
EFFICIENCY
Two types of tests on one cassette with quick result
Affordable, easy-to-use SARS-CoV-2 test kit Affordable, easy-to-use SARS-CoV-2 test kit Application Application Rapid antigen tests perform best when the person is tested in the early stages of infection with SARS-CoV-2
when viral load is generally highest. They also may be informative in diagnostic testing situations in which
the person has a known exposure to a confirmed case of COVID-19.
Rapid antigen tests can be used for screening testing in high-risk congregate settings in which repeat testing could quickly identify persons with a SARS-CoV-2 infection to inform infection prevention and control measures,
thus preventing transmission.
Benefits Benefits
Rapid test within 15 min.
Easy operation
Good specificity
A short window
* 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
Antibody rapid test kits:
Our test kits are superior in sensitivity and specificity. All have CE and FDA registration. Now we are able to offer these same goods and services to your establishment.
Delivery 14 days.
If you are interested, please do not hesitate to contact us.
Thank you for your kind attention.
Best regards.
Chaveng Munchantip (George)
Director (Medical Supplies)
Antibody rapid test kits:
Our test kits are also superior in sensitivity and specificity. All have CE and FDA registration. Now we are able to offer these same goods and services to your establishment.
Delivery 14 days.
If you are interested, please do not hesitate to contact us.
Thank you for your kind attention.
Best regards.
Chaveng Munchantip (George)
Director (Medical Supplies)
1752 Rapid Test Kits Suppliers
Short on time? Let Rapid Test Kits sellers contact you.