I-COVID-19 & Influenza A/B Rapid Test Kit

Incazelo emfushane:

Ikhithi Yokuhlola Okusheshayo ye-COVID-19 & Influenza A/B iyi-immunochromatographic ehloselwe ukutholwa ngokushesha kwe-in vitro qualitative kanye nokuhlukaniswa kwe-SARS-CoV-2, umkhuhlane A, nama-antigens omkhuhlane B kumhlinzeki wezempilo eqoqwe ngumhlinzeki we-nasopharyngeal swab kanye ne-oropharyngeal swab. , okuvela kubantu okusolwa ukuthi banegciwane lokuphefumula elihambisana ne-COVID-19 ngumhlinzeki wabo wezempilo.Izimpawu zomtholampilo kanye nezimpawu zokutheleleka ngegciwane lokuphefumula ngenxa ye-COVID-19 kanye nomkhuhlane zingafana.

I-SARS-CoV-2, i-influenza A kanye nama-antigens omkhuhlane B ngokuvamile atholakala ezibonelweni zokuphefumula ngesikhathi sesigaba esibi kakhulu sokutheleleka.Imiphumela emihle ikhombisa ukutheleleka okusebenzayo kodwa ayikukhiphi ukutheleleka ngebhaktheriya noma ukuthelelana kanye namanye amagciwane angatholwanga ukuhlolwa.Ukuxhumana komtholampilo nomlando wesiguli kanye nolunye ulwazi lokuxilonga kuyadingeka ukuze kunqunywe isimo sokutheleleka kwesiguli.I-ejenti etholiwe ingase ingabi imbangela eqondile yesifo.Imiphumela engemihle ayivimbeli i-SARS-CoV-2, umkhuhlane A, kanye/noma ukutheleleka komkhuhlane B futhi akufanele isetshenziswe njengesisekelo sodwa sokuxilongwa, ukwelashwa noma ezinye izinqumo zokuphatha isiguli.Imiphumela engemihle kufanele ihlanganiswe nokubhekwa komtholampilo, umlando wesiguli, kanye/noma ulwazi lwe-epidemiological.


Imininingwane Yomkhiqizo

Omaka bomkhiqizo

Isimiso

Ikhithi Yokuhlola Okusheshayo ye-COVID-19 & Influenza A/B isuselwe kumgomo we-qualitative immunochromatographic assay ukuze kutholwe i-SARS-CoV-2 kanye ne-Influenza A no-B kusuka kumasampula e-nasopharyngeal swab kanye namasampula e-oropharyngeal swab (I-Nasal swab kanye namasampula e-Oropharyngeal swab ) ezigulini okusolwa ukuthi zine-COVID-19 kanye/noma Umkhuhlane A kanye/noma Umkhuhlane B.

I-Strip 'COVID-19 Ag' iqukethe ulwelwesi lwe-nitrocellulose olumbozwe ngaphambili ngamasosha omzimba egundane alwa ne-SARS-CoV-2 kulayini wokuhlola (umugqa we-T) kanye nama-anti-mouse polyclonal antibodies kulayini wokulawula (umugqa C).Iphedi ye-conjugate ifuthwe ngesixazululo esibhalwe ngegolide (igundane le-monoclonal antibodies anti-SARS-CoV-2).I-Strip 'Flu A+B' iqukethe ulwelwesi lwe-nitrocellulose olugqitshwe ngaphambili ngamasosha omzimba egundane e-anti-Influenza A emgqeni 'A', amasosha omzimba egundane alwa nomkhuhlane B emgqeni 'B' kanye namasosha omzimba e-polyclonal embuzi avuliwe. ulayini wokulawula (umugqa C).Iphedi ye-conjugate ifuthwe ngesisombululo esibhalwe ngegolide (ama-mouse monoclonal antibodies anti-influenza A no-B)

Uma isampula liku-SARS-CoV-2 positive, ama-antigen esampula asabela ngama-anti-SARS-CoV-2 monoclonal amasosha omzimba abhalwe ngegolide ku-Strip 'COVID-19 Ag' ebikade yomiswe ngaphambili ku-conjugate pad. .Izingxube zibe sezithwetshulwa kulwelwesi ngamasosha omzimba e-SARS-CoV-2 ahlanganiswe ngaphambili futhi umugqa obomvu uzobonakala emigqeni ekhombisa umphumela omuhle.

Uma isampula inguMkhuhlane A kanye/noma B positive, ama-antigen esampula asabela nge-anti-Influenza A ebhalwe ngegolide kanye/noma amasosha omzimba e-monoclonal ku-Strip 'Flu A+B', omiswe ngaphambilini i-conjugate pad.Izingxube zibe sezithwetshulwa kulwelwesi ngamasosha omzimba oMkhuhlane A kanye/noma ama-B ahlanganiswe ngaphambili kanye nomugqa obomvu uzobonakala emigqeni yawo ekhombisa umphumela omuhle.

Uma isampuli inegethivu, abukho ubukhona be-SARS-CoV-2 noma i-Influenza A noma i-Influenza B noma ama-antigens akhe angaba khona ekuhlanganiseni okungaphansi komkhawulo wokutholwa (LoD) lapho imigqa ebomvu ingeke ivele khona.Ukuthi isampula liphozithivu noma cha, emicu emi-2, imigqa engu-C izohlala ivela.Ukuba khona kwale migqa eluhlaza kusebenza njengalokhu: 1) ukuqinisekisa ukuthi ivolumu eyanele yengezwa, 2) ukuthi kutholakala ukugeleza okufanele kanye 3) nokulawula kwangaphakathi kwekhithi.

Izici Zomkhiqizo

Ukusebenza kahle: 3 ekuhlolweni oku-1

Imiphumela esheshayo: imiphumela yokuhlolwa emizuzwini eyi-15

Okuthembekile, ukusebenza okuphezulu

Kalula: Ukusebenza okulula, akukho mishini edingekayo

Isitoreji Esilula: Izinga lokushisa legumbi

Ukucaciswa Komkhiqizo

Isimiso I-Chromatographic immunoassay
Ifomethi Ikhasethi
Isitifiketi CE
Isifanekiso I-swab yamakhala / i-Nasopharyngeal swab / i-Oropharyngeal swab
Ukucaciswa 20T / 40T
Izinga lokushisa lesitoreji 4-30 ℃
Impilo yeshelufu Izinyanga ezingu-18

Uku-oda Ulwazi

Igama lomkhiqizo Pakisha Isifanekiso
I-COVID-19 & Influenza A/B Rapid Test Kit 20T / 40T I-swab yamakhala / i-Nasopharyngeal swab / i-Oropharyngeal swab

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