Ikhithi yakwa-SARS-CoV-2 Antigen

  • SARS-CoV-2 Antigen Rapid Test

    Ukuhlolwa Okusheshayo Kwe-SARS-CoV-2

    I-Dual Biosafety System Device ye-SARS-CoV-2 Antigen Test isetshenziselwa ukuthola ikhwalithi ye-novel coronavirus (SARS-CoV-2) nucleocapsid (N) antigen kumasampuli womuntu we-Throat / Nasopharyngeal swab in vitro. Ikhithi kufanele isetshenziswe kuphela njengenkomba yokungezelela noma isetshenziswe ngokuhlangana nokutholwa kwe-nucleic acid ekutholeni amacala okusolwa we-COVID-19. Ayikwazi ukusetshenziswa njengesisekelo sodwa sokuxilongwa nokushiywa ngaphandle kweziguli ze-pneumonitis ezitheleleke nge-coronavirus yenoveli, futhi ayifanele ukuhlolwa kwabantu abaningi. Amakhithi afanele kakhulu ukusetshenziselwa ukuhlolwa okukhulu emazweni nasezifundeni lapho ukuqubuka kwenoveli coronavirus kusakazeka ngokushesha, kanye nokunikeza ukuxilongwa nokuqinisekiswa kokutheleleka nge-COVID-19.

    OKUBALULEKILE: Lo mkhiqizo uhlose ukusetshenziselwa ubuchwepheshe kuphela, HHAYI UKUZIVIVINYA NOMA UKUHLOLA EKHAYA!

  • Dual Biosafety System Device for SARS-CoV-2 Antigen Rapid Test

    Idivayisi Yesistimu Ye-Dual Biosafety ye-SARS-CoV-2 Antigen Rapid Test

    I-Dual Biosafety System Device ye-SARS-CoV-2 Antigen Test isetshenziselwa ukuthola ikhwalithi ye-novel coronavirus (SARS-CoV-2) nucleocapsid (N) antigen kumasampuli womuntu we-Throat / Nasopharyngeal swab in vitro. Ikhithi kufanele isetshenziswe kuphela njengenkomba yokungezelela noma isetshenziswe ngokuhlangana nokutholwa kwe-nucleic acid ekutholeni amacala okusolwa we-COVID-19. Ayikwazi ukusetshenziswa njengesisekelo sodwa sokuxilongwa nokushiywa ngaphandle kweziguli ze-pneumonitis ezitheleleke nge-coronavirus yenoveli, futhi ayifanele ukuhlolwa kwabantu abaningi. Amakhithi afanele kakhulu ukusetshenziselwa ukuhlolwa okukhulu emazweni nasezifundeni lapho ukuqubuka kwenoveli coronavirus kusakazeka ngokushesha, kanye nokunikeza ukuxilongwa nokuqinisekiswa kokutheleleka nge-COVID-19. Ukuhlolwa kukhawulelwe kumalabhorethri aqinisekiswe ngaphansi kwemithetho yeziphathimandla zikazwelonke noma zendawo.

  • System Device for SARS-CoV-2 & Influenza A/B Combo Antigen Rapid Test

    Idivayisi Yesistimu ye-SARS-CoV-2 ne-Influenza A / B Combo Antigen Rapid Test

    IStrongStep® System Device ye-SARS-CoV-2 & Influenza A / B Combo Antigen Rapid Test isebenzisa i-chromatographic lateral flow test. Kunemichilo emithathu kudivayisi ethola i-SARS-CoV-2, uhlobo lomkhuhlane u-A nohlobo lomkhuhlane B ngokulandelana, i-Latex conjugated antibody (Latex-Ab) ehambelana ne-SARS-CoV-2 / Flu A / Flu B ayomile ukuphela komugqa ngamunye we-nitrocellulose ulwelwesi. Ama-antibody e-SARS-CoV-2 / Flu A / Flu B ayibhondi e-Test Zone (T) kanti i-Biotin-BSA iyisibopho e-Control Zone (C) emgqeni ngamunye. Lapho isampula lengezwa, lifuduka ngokusabalalisa kwe-capillary ukuvuselela i-latex conjugate. Uma ekhona kusampula, ama-antigen e-SARS-CoV-2 / Flu A / Flu B azobopha ngama-antibodies amancane ahlanganisiwe akha