I-SARS-CoV-2

  • Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    Inoveli Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit

    I-coronavirus yenoveli iyigciwane le-RNA, eliqukethe amaprotheni nama-nucleic acid. Leli gciwane lingena emzimbeni womuntu ophethe (umuntu), lingene kumaseli ngendawo ebophayo ehambelana ne-receptor ACE2, bese liyaziphindaphinda kumaseli aphethe, okwenza amasosha omzimba omuntu aphendule kubahlaseli bakwamanye amazwe futhi akhiqize amasosha omzimba athile. Ngakho-ke, i-vial nucleic acid nama-antigen, nama-antibodies athile abhekene ne-coronavirus yenoveli angasetshenziswa njengama-biomarker athile wokuthola i-coronavirus yenoveli. Ngokuthola i-nucleic acid, ubuchwepheshe be-RT-PCR busetshenziswa kakhulu.

    I-Novel Coronavirus (SARS-CoV-2) Multiplex Real-Time PCR Kit yenzelwe ukuthi isetshenziselwe ukuthola ukutholakala kwekhwalithi ye-SARS_CoV-2 virus RNA ekhishwe kuma-nasopharyngeal swabs, oropharyngeal swabs, sputum kanye ne-BALF ezigulini ezihambisana ne-FDA / CE Uhlelo lokukhishwa kwe-IVD namapulatifomu we-PCR aqokiwe abhalwe ngenhla.

    Ikhithi yenzelwe ukusetshenziswa ngabasebenzi abaqeqeshiwe elebhu

  • SARS-CoV-2 IgM/IgG Antibody Rapid Test

    Ukuhlolwa Okusheshayo Kwe-SARS-CoV-2 IgM / IgG

    IStrongStep®  I-SARS-CoV-2 IgM / IgG Antibody Rapid Test kit isetshenziselwa ukutholakala kwekhwalithi ye-in vitro kanye nokuhlonza isifo se-SARS-CoV-2 antibody coronavirus COVID-19 kuma-serum / plasma / amasampula egazi lonke (kufaka phakathi igazi le-venous kanye negazi lokuhlaba ngomunwe) ezigulini ezisolwayo ukuxilongwa kokutheleleka kungasetshenziselwa ukuxilonga abantu abanezimpawu noma abangenazimpawu abanokutheleleka okunamandla nokuhlolwa kwamangqamuzana noma imininingwane yezempilo.

    Ukuhlolwa kukhawulelwe e-US ukusatshalaliswa kumalabhorethri aqinisekiswe yi-CLIA ukwenza ukuhlolwa okuphezulu kakhulu.

    Lokhu kuhlolwa akukabuyekezwa yi-FDA.

    Imiphumela emibi ayikuvimbeli ukutheleleka okunamandla kwe-SARS-CoV-2.

    Imiphumela evela ekuhlolweni kwe-antibody akufanele isetshenziselwe ukuxilonga noma ukukhipha ukutheleleka okunamandla kwe-SARS-CoV-2.

    Imiphumela emihle ingabangelwa ukutheleleka okwedlule noma kwamanje ngezinhlobo ezingezona ze-SARS-CoV-2 coronavirus, njenge-coronavirus HKU1, NL63, OC43, noma i-229E.

  • 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