I-Antigen SARS-CoV-2 Antigen Rapid Test Kit (uHlelo lweTRFIA)

Inkcazelo emfutshane:

I-SHANGHAI Binicare Co., LTD ibandakanyeka kwi-vitro diagnostic (IVD) iimveliso zeCoronavirus, ezibandakanya uvavanyo lwe-antigen olukhawulezayo kunye nezixhobo zokuvavanya i-antibody.Umzi-mveliso wethu useQingdao, kwaye isebe lokuthengisa le-ofisi eyintloko liseShanghai.Siyiarhente yehlabathi yeQingdao AIBO Diagnostic Co., LTD.I-Anti SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) isebenzisa itekhnoloji ye-Fluorescence Immunochromatographic Assays (TRFIA) itekhnoloji yokufumanisa i-SARS-CoV-2 virus nucleocapsid protein, eyiprotein ebalulekileyo egciniweyo ye-SARS-CoV-2 Iisampulu zabantu ngeempumlo/oropharyngeal.Ukufunyaniswa kwe-SARS-CoV-2 ye-nucleocapsid protein antigen inokusetyenziselwa ukuncedisa ukufunyaniswa kosulelo lwe-coronavirus entsha, kwaye iluncedo ekubhaqweni kwangoko kosulelo lwenyumoniya lwe-coronavirus ngexesha elifihlakeleyo.

Thumela i-imeyile kuthi

Iinkcukacha zeMveliso

Iithegi zeMveliso

Uvavanyo lwemigaqo

I-SARS-CoV-2Antigen Rapid Test Kit (TRFIA) luvavanyo lwesangweji ye-immunofluorescent. Ukufunyanwa kwe-SARS-CoV-2 nucleocapsid protein antigen ingasetyenziselwa ukufumanisa isifo sentsholongwane ye-corona, kwaye iluncedo ekubhaqweni kwangoko kwenoveli. Usulelo lwentsholongwane ye-corona inyumoniya kwixesha elifihliweyo.Umcu wovavanyo uneenwebu eziqatywe ngaphambili ngempuku echasene ne-CoV N ye-protein ye-monoclonal antibodies kwimigca yovavanyo.Xa isampulu isetyenziswa kwisampulu yamaqula, iprotein ye-SARS-CoV N kunye neelebhile ze-antibody complexes ziyenziwa kwaye zinyuke ngomcu.I-microsphere fluorescent probe reagent ebhaliweyo isetyenziselwa ukwenza umgca obomvu obonakalayo onetotshi ye-UV ehambelanayo.Ubukho be-SARS-CoV-2 buya kuboniswa ngumgca wovavanyo obomvu obonakalayo (T) kwifestile yeziphumo.I-Membrane ifakwe ngaphambili kunye neChicken IgY kumgca wolawulo (C).Ulayini wolawulo (C) uvela kwifestile yesiphumo ngasinye xa isampulu ihambe ngomcu.Umgca woLawulo usetyenziswa njengolawulo lwenkqubo.Umgca wokulawula kufuneka uhlale ubonakala xa inkqubo yokuvavanya iqhutywe ngokufanelekileyo kwaye i-reagents isebenza njengoko ijoliswe kuyo.Uvavanyo lwe-antigen olukhawulezileyo sisixhobo sokuxilonga, kodwa asenzelwanga ukuqinisekisa usulelo olusebenzayo okanye ukuthintela usulelo phakathi kwabantu abangenazo iimpawu.Zenzelwe abantu abaneempawu ze-COVID-19, abantu abasondelelene nomntu oqinisekisiweyo we-COVID, kunye nokulandelela abantu abayinxalenye yoqhambuko.

Ukutolikwa kweAssay

Ye-TRFIA analyzer-Utoliko lweZiphumo.Iziphumo zibalwa ngokuzenzekelayo kwaye ziboniswe kwisikrini.Iziphumo zesampulu ziya kuboniswa ngexabiso lesiginali kunye neleyibhile ethi "negative", "positive" okanye "ERROR".
Ukutolikwa kweziphumo:

20201216142629_9935
Ukupakisha Iinketho

No	Ukupakisha iNgcaciso	Imihlubu	Ikhadi le-IC (Ngokuzithandela)	Ngempumlo/Oropharyngeal Swab (Ngokuzikhethela)	Ukutsalwa Umbhobho	Ibhotile yeReagent yokukhupha
1	1 uvavanyo / ibhokisi	1	1	1	1	1
2	Iimvavanyo ezi-5 / ibhokisi	5	1	5	5	5
3	Iimvavanyo ezingama-25 / ibhokisi	25	1	25	25	25
4	Iimvavanyo ezingama-50 / ibhokisi	50	1	50	50	50