Ikhithi yovavanyo olukhawulezayo olukhawulezayo lwe-Covid-19 yovavanyo lwe-antigen yempumlo ye-swab
UKUSETYENZISWA OKUHLOSIWEYO
I-SARS-CoV-2 ye-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 lwesigulane (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!