Ikhithi Yokuhlola Esheshayo ye-Anti SARS-CoV-2 Antigen Rapid (Ushicilelo lwe-TRFIA)

Incazelo emfushane:

I-SHANGHAI Binicare Co.,LTD yenza imikhiqizo ye-vitro diagnostic (IVD) Coronavirus, ehlanganisa ukuhlolwa kwe-antigen okusheshayo kanye nezinsiza zokuhlola i-antibody.Ifektri yethu itholakala eQingdao, kanti umnyango wezokuthengisa wehhovisi elikhulu useShanghai.Siyi-ejenti yomhlaba wonke ye-Qingdao AIBO Diagnostic Co., LTD.I-Anti SARS-CoV-2 Antigen Rapid Test Kit (TRFIA) isebenzisa ubuchwepheshe be-Time Resolved Fluorescence Immunochromatographic Assays (TRFIA) ukuthola i-SARS-CoV-2 virus nucleocapsid protein, okuyiphrotheni ebalulekile elongiwe yesakhiwo ye-SARS-CoV-2 amasampula ekhala / oropharyngeal womuntu.Ukutholwa kwe-SARS-CoV-2 nucleocapsid protein antigen kungasetshenziswa ukusiza ukuhlonza ukutheleleka kwe-coronavirus yenoveli, futhi kuyasiza ekutholakaleni kusenesikhathi kwenoveli i-coronavirus pneumonia ukutheleleka esikhathini esicashile.


Imininingwane Yomkhiqizo

Omaka bomkhiqizo

Izimiso Zokuhlola

I-SARS-CoV-2Antigen Rapid Test Kit (TRFIA) iwukuhlola isangweji le-immunofluorescent. Ukutholwa kwe-SARS-CoV-2 nucleocapsid protein antigen kungasetshenziswa ukusiza ukuhlonza ukutheleleka ngegciwane le-corona, futhi kuyasiza ekutholweni kwenoveli kusenesikhathi. i-corona virus pneumonia infection in the latent period.Umucu wokuhlola uqukethe ulwelwesi olumbozwe ngaphambili ngamasosha omzimba egundane e-anti-CoV N amaprotheni emigqeni yokuhlola.Lapho isampula lisetshenziswa emithonjeni yesampula, kwakheka amaprotheni e-SARS-CoV N nama-antibody complexes anelebula futhi akhuphuke ngomugqa.I-microsphere fluorescent probe reagent enelebula isetshenziselwa ukwenza ulayini obomvu obonakalayo onethoshi le-UV elifaniswe.Ukuba khona kwe-SARS-CoV-2 kuzobonakala ngomugqa wokuhlola obomvu obonakalayo (T) efasiteleni lemiphumela.I-Membrane imbozwe ngaphambili ngeChicken IgY kulayini wokulawula(C).Ulayini wokulawula(C) uvela ewindini ngalinye lomphumela lapho isampula ligeleza emgqeni.Ulayini Wokulawula usetshenziswa njengokulawula inqubo.Ulayini wokulawula kufanele uhlale uvela lapho inqubo yokuhlola yenziwa kahle futhi ama-reagents asebenza ngendlela ehlosiwe.Ukuhlolwa kwe-antigen okusheshayo kuyithuluzi lokuxilonga, kodwa akuhloselwe ukuqinisekisa ukutheleleka okusebenzayo noma ukuvimbela ukusulelana phakathi kwabantu abangenazo izimpawu.Zenzelwe abantu abanezimpawu ze-COVID-19, abantu abasondelene kakhulu necala le-COVID eliqinisekisiwe, kanye nokulandelela abantu abayingxenye yokugqashuka.

Ukuhunyushwa Kwe-Assay

Okokuhlaziya kwe-TRFIA-Ukutolikwa Kwemiphumela.Imiphumela ibalwa ngokuzenzakalelayo futhi iboniswe esikrinini.Imiphumela yesampula izoboniswa ivelu yesiginali kanye nelebula ethi "negative", "positive" noma "ERROR".
Ukuhunyushwa Kwemiphumela:

20201216142629_9935
Ukupakisha Izinketho

No Ukupakisha Ukucaciswa Imichilo Ikhadi le-IC (Uma uthanda) Ikhala/Oropharyngeal
I-Swab (Uma uthanda)
Isizinda
Ithubhu
Ibhodlela le-Reagent yokukhipha
1 1 ukuhlolwa / ibhokisi 1 1 1 1 1
2 5 ukuhlolwa / ibhokisi 5 1 5 5 5
3 25 ukuhlolwa / ibhokisi 25 1 25 25 25
4 50 ukuhlolwa / ibhokisi 50 1 50 50 50
20201216151015_5890

Ifekthri

ifektri (5)
ifektri (2)
ifektri (3)
3qq

  • Okwedlule:
  • Olandelayo:

  • Imikhiqizo Ehlobene