Ikhithi yovavanyo olukhawulezayo olukhawulezayo lwe-Covid-19 yovavanyo lwe-antigen yempumlo ye-swab
UKUSETYENZISWA OKUHLOSIWEYO
I-SARS-CoV-2 i-Antigen Rapid Test (i-Colloidal Gold) yenzelwe ukufunyaniswa komgangatho we-SARS-CoV-2 Antigen (iprotein ye-Nucleocapsid) kwisampulu ze-swab zempumlo kwi-vitro.Iziphumo ezilungileyo zibonisa ubukho be-antigen ye-SARS-CoV-2.Kufuneka ifunyaniswe ngakumbi ngokudibanisa imbali yesigulana kunye nolunye ulwazi loxilongo .Iziphumo ezilungileyo azibandakanyi usulelo lwebhaktheriya okanye olunye usulelo lwentsholongwane.Iintsholongwane ezifunyenweyo azingoyena nobangela uphambili weempawu zesifo.Iziphumo ezibi azilubandakanyi usulelo lwe-SARS-CoV-2, kwaye akufuneki ibe kuphela kwesiseko sonyango okanye izigqibo zolawulo lwezigulane (kubandakanywa nezigqibo zolawulo losulelo).Nika ingqalelo kwimbali yoqhagamshelwano yamva nje yesigulana, imbali yonyango kunye neempawu ezifanayo kunye neempawu ze-COVID-19, ukuba kuyimfuneko, kuyacetyiswa ukuba uqinisekise ezi sampuli ngovavanyo lwe-PCR kulawulo lwesigulana.Yeyabasebenzi baselabhoratri abafumene isikhokelo okanye uqeqesho lobuchwephesha kwaye banolwazi lobuchwephesha lokuxilongwa kwe-in vitro, kunye nabasebenzi abafanelekileyo abafumene ulawulo losulelo okanye uqeqesho lokonga.
Wamkelekile kuqhagamshelwano ngeenkcukacha ezithe vetshe!