Uvavanyo lwe-SARS-CoV-2 IgG / IgM olukhawulezayo

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

    I-SARS-CoV-2 IgM / IgG yovavanyo olukhawulezileyo lwe-Antibody

    IStrongStep®  I-SARS-CoV-2 IgM / IgG ye-Antibody Rapid Test kit isetyenziselwa ukubonwa kwe-vitro esemgangathweni kunye nokuchongwa kwesifo se-SARS-CoV-2 antibody coronavirus COVID-19 kwiserum / iplasma / iisampulu zegazi (kubandakanya igazi le-venous kunye negazi lomnwe). yezigulana ezikrokrelwayo ukuxilongwa kosulelo kunokusetyenziselwa ukufumanisa ukuba umntu uneempawu okanye umntu ongenasifo osulelayo kunye novavanyo lweemolekyuli okanye ulwazi lweklinikhi.

    Uvavanyo lilinganiselwe e-US ukusasazwa kwiilebhu eziqinisekiswe yi-CLIA ukwenza uvavanyo oluntsonkothileyo oluphezulu.

    Olu vavanyo aluzange luhlolwe yi-FDA.

    Iziphumo ezingalunganga aziluthinteli usulelo lwe-SARS-CoV-2.

    Iziphumo zovavanyo lwe-antibody akufuneki zisetyenziselwe ukuxilonga okanye ukukhuphela ngaphandle usulelo lwe-SARS-CoV-2.

    Iziphumo ezincumisayo zinokuba ngenxa yosulelo oludlulileyo okanye olukhoyo ngezifo ezingezizo ze-SARS-CoV-2 coronavirus, ezinje nge-coronavirus HKU1, NL63, OC43, okanye 229E.