* 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
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
Number of Reactions(Preps)/Kit :30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK019-30
STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.
Easy to use, Easy to read and interpret
Discrimination between HIV-1 and HIV-2 antibodies
Room temperature storage
Performance
Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)
A serology test or Antibody Rapid Test which doesn't test for the virus itself. Instead, it look for body's immune response to the virus. This test is getting popular is not only because its convenience but also because it can identify whether youâ??ve ever been exposed to SARS-CoV-2 - which would deepen our understanding of who is getting sick, particularly people who showed few or no symptoms. It could also allow people whose bodies seem to have some degree of immunity to the illness to return to work more quickly.
Please email us and get detailed factsheet, certification etc.
GOLD STANDARD for diagnosis novel coronavirus. This kit is based on one-step RT-PCR technique. Used for the in vitro qualitative detection of novel coronavirus (2019-nCoV) ORF1ab and N gene in the throat swabs, sputum specimens of suspected pneumonia patients infected by novel coronavirus, suspected clustering cases and others needing diagnosis or differential diagnosis for novel coronavirus.
No cross-reaction, sensitivity is 500 copies/ml. CFDA/CE. Applicable Instruments include ABI 7500 & LightCycler480.
Celltrion DiaTrust COVID-19 Ag Rapid Test is a lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid and receptor binding domain (RBD) antigens in direct mid-turbinate nasal swab specimens. Results are for the identification of SARS-CoV-2 nucleocapsid and RBD protein antigens.
We provide stable supply of Celltrion DiaTrustâ?¢ COVID-19 Ag Rapid Test kits in large quantities.
Available Versions: Professional and Home Use.
For serious purchasers, please contact us at sales@mtod.sg for a quotation. Price listed is only indicative and not the final.
2019-nCoV Neutralizing Antibody Test Kit
Fluorescence Immunochromatography
(Serum/plasma)
Rapid Test: Just for 15 Minutes
Accurate Result: Fluorescence immunoassay, high sensitivity
Convenient operation with smart POCT analyzers
Rate COVID-19 Vaccine immediately
Application
By testing neutralizing antibody titer after COVID-19 Vaccination,
it will be able to figure out the vaccine efficiency
Product Information
Product Name: 2019-nCoV Neutralizing Antibody Determination Kit
Methodology:Fluorescence immunoassay
Size:25 Tests/box
Storage and Validity:Stored at 2-30 within 18 months
Specimen:-Clinical fresh human serum, recommended EDTA anticoagulant plasma
Easy Operation:
1 Take 100 sample to buffer and mix 5-10s
2 Add 80 mixed sample to strip
3 Incubation time: 15 mins
4 Put strip into analyzer to test
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CAT No : RCHM-02071. The CareStar COVID-19 Antigen test is a lateral flow immunochromatographic assay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal or anterior nasal swab specimens directly collected from individuals who are either suspected of COVID-19 by their healthcare provider within first five days of symptom onset, or from individuals without symptoms or other epidemiological reasons to suspect COVID-19 when tested twice over two or three days with at least 24 hours and no more than 48 hours between tests.
