Uhlu Olujwayelekile Lokuhlola Ukuhlolwa Okusheshayo kwe-Antigen
Uhlu Olujwayelekile Lokuhlola Ukuhlolwa Okusheshayo kwe-Antigen
Ukukhishwa kusuka kumbiko wokuhlola umtholampilo we-3rd Part
I-Immuno Biotech Antigen Rapid Test iyi-Assay engasetshenziselwa ukutholwa kwe-SARSCOV - 2 Ukutheleleka. Lokhu kubona kuvivinya ubukhona be-SARS - I-COV - 2 n - Amaprotheni yi-Swab specimen. Kulolu cwaningo, i-immuno biotechI-Antigen Rapid Testyahlolwa nge-roche sars - Cov - 2 ngokusheshaIsivivinyo se-AntigenNasal ne-PCR. IPerkinelmer Reverse realcriptase real time polymerase chain reaction (RT - I-RT - QPCR) isetshenziselwe ukuhlaziywa okungafani. Sekukonke, i-80 engemihle ne-40 yesikhathi esihle - Amasampula ayi-19 afakiwe kulokhu kuqhathanisa. Ukuzwela kwe-Immuno BiotechI-Antigen Rapid Testwayezimisele ukuba ngu-92,5% (95% CI: 86,4% - 96,0%). Ngezansi kwenani le-CP le-32.6 ukuzwela kwakungu-100%. Ukucaciswa okungu-100% (95% CI: 96,9% - 100%) nokunemba kwama-97,5% CI: 95% CI: 95% CI: 95,1% - 99,1% - 99,1%). Ukuhlolwa okusheshayo kwe-Immuno nge-antigen esheshayo kutholakele zonke izinhlobo eziyishumi nantathu zakwa-SARS - I-Cov - 2 Iphaneli Ehlukile 1 no-2. Kodwa-ke, okuhlukile 2730 kwatholwa njengenhle. Ukuhlushwa okuphansi okuphansi bekungaphezulu kuka-140.000 DPCR amakhophi / ml. Ukuhlolwa okusheshayo kwe-Roche Antigen kwadingeka impela imiphumela efanayo futhi yathola amasampula afanayo ane-FALL. Ngaphezu kwalokho, ukuhlolwa okusheshayo kwe-Roche Antigen kwakhombisa umkhawulo wokutholwa okuzungeza amakhophi angama-140.000 DPCr amakhophi / ml. Ukusebenza kokuhlolwa okusheshayo kwe-Antigen kuyafana kulokhu kuhlolwa.
Ungakhathazeka ngokuthi imikhiqizo yethu ingabona i-ACOVID ehlanganisiwe - Izinhlobo eziyi-19?
Ngaphandle kwe-covic delta strain, muva nje, abakwa-SARS - I-COV - 2 entsha ehlukile ye-Omicron (B.1.1.529) Izingqinamba zazisakazeka zivela eNingizimu Afrika nasemhlabeni wonke futhi zenza kube nzima ukuvikela nokulawula. Izindawo zokuguqulwa kwe-NucLeocapsid Protein (n Amaprotheni) zitholakala ku-DEL31 / 33, P13L, R203K, kanye ne-G204r, indawo ye-A173, i-NTD esifundeni) ibonwa ngababili bethu. Ngakho-ke, abakwa-SARS - I-Cov - 2 Antigen Rapid Test (COVID - 19 AG) inekhono ngokweqiniso lokutholwa kwa-SARS - I-2 New Vavint Omicron Strains.
Okwamanje, abakwa-SARS bethu - I-Cov - 2 Antigen Rapid Test (COVID - 19 AG)namanje ukusebenzaAbathintekayo amabala ahlukile kumaprotheni abo, kufaka phakathi okuhlukile e-UK B.1.1.7, iBrazil Variant P.1.351, kanye ne-India variants B.1.617 no-B.1.617.2.
Mayelana nekhwalithi yeI-COVID - 19 3 ku-1 Antigen Test Omicron Delta ngokushesha Test ?
Kusukela ekuqaleni kwendawo - Ubhubhane lwaba-19, izilingo zethu zasebenzisa ubuchwepheshe babo ukuthuthukisa imikhiqizo ehlobene nokutholwa kwe-COVID - 19. UkusukaI-COVIAL IGG / IGM AntiBODY TEST to Cavid Antigen Testna-Caving NUETRATIZING ANTIBODY TEST. Sibe nomthelela emzameni othobekile emsebenzini wokuvimbela ubhubhane emhlabeni.
I-Immuno Covion Antigen Test isetshenziswa ezikhungweni zokuhlola kanye nezibhedlela ku-I-Argentina, Germany, Italy, iRomania, ePoland, i-United Kingdom, eDenmark nakwamanye amazwe. Siyadunyiswa ukuthola ukwethembana nokwazisa ngemikhiqizo yethu evela kochwepheshe abavela emazweni ahlukahlukene.
Mayelana ne-Immunobio
Singukuphakama kwezwe lonke - I-Tech Enterprise enowakho ukukhiqizwa, R & D, kanye nokuthekelisa amaqembu.
Kusukela ukugqashuka kwe-New Vovisious Esekupheleni kuka-2019, sesiqalile ukuthuthukisaI-COVID - Ukuhlolwa okungu-19imikhiqizo.
NgoFebhuwari 2020, ezinyangeni ezi-2 nje, sathuthukisa ngempumelelo IGG / IGM Antibody Test futhi ukhombise ukusekelwa okuqinile e-Argentina.
Ngo-Agasti 2020, sathuthuka ngempumelelo I-COVIC - I-19 Antigen Test futhi unikeze okuphezulu - Imikhiqizo yekhwalithi eya eJalimane.
Ukubona ukuthi i-Covid - I-19 ingaba yi-su offines ekwazi ukudedelwa kuphela ngokugoma umuthi, nokuthi imigomo yangaphambilini ayizange iqinisekiswe ngokuphelele yi-populaion, saqala ukwethula Ukuvikelwa kokuhlolwa kwe-antibod. Ukuqinisekisa ukusebenza kahle kwemithi yokugoma kulelo ngakunye kunezela ungqimba lokuvikelwa ekuvinjelweni kwesifo.
Inqubo yokuhlola
Vumela idivaysi yokuhlola, i-specimen, buffer, kanye / noma izilawuli ukulingana nokushisa kwegumbi (15 - 30 ° C) ngaphambi kokuhlolwa.
1. Letha isikhwama sokushisa segumbi ngaphambi kokuvula. Susa idivaysi yokuhlola kusuka esikhwameni esivaliwe bese uyisebenzisa ngokushesha okukhulu.
2. Beka idivaysi yokuhlola endaweni ehlanzekile nevundlile. Buyisela emuva ishubhu leqoqo le-specimen, khipha amaconsi ama-3 we-specimen elungiselelwe ku-specimen kahle () Hlola ikhasethi bese uqala isibali sikhathi.
Bheka umfanekiso ngezansi.
3. Lindela umugqa onemibala ukuze uvele. Funda imiphumela ngemizuzu eyi-10. Ungahumushi umphumela ngemuva kwemizuzu engu-15.
Lapho kukhiqizwa khona ama-kits wokuhlola?
Isitshalo sokukhiqiza se-GMP
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