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)
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COVID-19 Ag Rapid Test Device is an in vitro diagnostic rapidtest for the qualitative detection of antigen (Ag) in humannasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. COVID-19 Ag RapidTest Device is for professional use only and is intended to be used asan aid in the diagnosis of
COVID-19 serology test.Cellex qSARS-CoV-2 IgG/IgM Rapid Test.qSARS-CoV-2 IgG/IgM Rapid Test Cassette.FDA Grants Emergency Authorization for First Rapid Antibody Test for COVID-19
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.
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.
Universal Transport Medium -Kit is a specially designed transport system to collect and transport viruses in an active form to the laboratory for isolation. It is designed to maintain the viability and virulence of the viral sample.
Appearance-Orange cultured clear solution, pH at 25 C=7.0 0.5
3mL of Media in a sterilized tube with two swabs in a kit
Features 1) Easy to use 2) Flexible Transport Temperature Ranges 3) Long-term preservation
4) Cost-efficient
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
The PocRoc SARS-CoV-2 Neutralizing Antibody Rapid Test Kit is developed for in vitro qualitative detection of SARS-CoV-2 neutralizing antibodies in human serum, plasma, or whole blood samples.
SARS-CoV-2 Neutralizing antibody is an important marker for assessing the effectiveness of the SARS-CoV-2 vaccines. The reagent is for neutralizing antibody detection in samples from individuals after vaccine injection or recovered from COVID-19. PocRoc�® SARS-CoV-2 Neutralizing Antibody Rapid Test Kit has great significance for the development of SARS-CoV-2 vaccines, evaluation of effectiveness, and evaluation of neutralizing antibody levels in human bodies.
For Medical Professional Use Only!
TEST PROCEDURE
Do not open the sealing strip until you are ready to perform a test, and the single-use test is suggested to be used under a low environment humidity (RHâ?¤70%) within 1 hour.
1. Allow all the components of the kit and specimens to reach room temperature prior to testing.
2. Take out the test card and place it on a clean dry surface.
3. Identify the test card for each specimen.
4. Use a dropper to deliver one drop (~40�¼l) of serum, plasma, or whole blood samples into the sample well on the test card, followed by one drop (~40l) of sample buffer.
5. Start the timer and read the result immediately after 15 minutes, and the result after 30 minutes is invalid.
