women health test kits, infectious diseases test kit.Transportation and shipping
Rapid antigen test kit, flua&flub antigen rapid test, malaria, dengue, hav, tb, h.p, fob, sypilis, monkey rapid test kit.Oem service
Covid 19 home test rdt, covid 19/flu combo rdt, vtm, swab, plastic ware; 96 well plate, barcode tube.
Medical test kits like hirikon hiv 1/2 saliva home test kits.
Canine cpv rapid test kit.
Rapid test kit, hiv, hbsag, hcv, malaria, dengue, typhoid.
Rapid Diagnostics Test Kit.
Rapid test, point of care testing(poct) device.
Canine CPV rapid test kit.
Antigen Kits, Dengue, Uti Test Kits.
Product Details: 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 rapid in vitro qualitative immunoassay for detection of antibodies to the Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) Clear, dependable results in 15 minutes Requires minimal training and no equipment So easy it can be used at the lowest levels of health care service Can use whole blood or serum/plasma Collection can be by fingerstick or venipuncture No refrigeration required Storage conditions 2-30�°C
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.
The performance of SARS-CoV-2 Antigen Rapid Test NOTE:Sign a contract with the distributor. If you want to sign a contract with the factory, please don't ask, Payment method : escrow bank,LC(Less than $350000ï¼? Welcome real buyers,Orders can be tested in small batches
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.
Antigen Test Kit (Colloidal Gold) Certified : US_FDA, Thai FDA, TGA, TUV, CE Marked Nasopharyngeal Swab , Oropharyngeal Swab, Limit of detection, The limit of detection has been evaluated at 0.5 ng/mL. Please note. due to high demand of product. First come, First Get terms applied. Price FOB
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
