COVID-19/Flu A&B Rapid Immunoassay ukuze ibonwe ngokuthe ngqo,
I-COVID-19/Flu A&B Rapid Immunoassay yokuFumana ngokuNgqo,
Ukusetyenziswa okucetywayo
I-SARS-CoV-2 kunye ne-Influenza A/B Antigen Combo Rapid Test Kit (Lateral chromatography) iza kusetyenziswa kunye nokubonakaliswa kweklinikhi kunye nezinye iziphumo zovavanyo lwaselabhoratri ukunceda ukuxilongwa kwezigulana ekurhaneleka ukuba yi-SARS-CoV-2 okanye i-Influenza A. /B usulelo.Uvavanyo kufuneka lusetyenziswe kuphela ziingcali zonyango.Ibonelela kuphela ngesiphumo sokuqala sovavanyo kwaye ezinye iindlela ezikhethekileyo zokuxilongwa kufuneka zenziwe ukuze kufunyanwe uqinisekiso lwe-SARS-CoV-2 okanye usulelo loMkhuhlane A/B.Ukusetyenziswa kobuchwephesha kuphela.
Umgaqo woVavanyo
SARS-CoV-2 & Influenza A/B Antigen Combo Rapid Test Kit (Lateral chromatography) yi-lateral flow chromatographic immunoassay.Ineziphumo ezimbini zeWindows.Ngasekhohlo kwii-antigens ze-SARS-CoV-2.Inemigca emibini egqitywe ngaphambili, "T" Umgca wovavanyo kunye no "C" Umgca wokulawula kwi-nitrocellulose membrane.Ngakwesokudla yifestile yesiphumo seFluA / FluB, inemigca emithathu efakwe ngaphambili, "T1" umgca woVavanyo lweFluA, "T2" umgca woVavanyo lweFluB kunye no "C" Umgca wokulawula kwi-nitrocellulose membrane.
Igama lemveliso | Ikati.Hayi | Ubungakanani | Umzekelo | Beka ubomi kwishelufa | Trans.& Sto.Temp. |
I-SARS-Cov-2 kunye ne-Influenza A&B Antigen Rapid Test Kit (Immunochromatographic Assay) | B005C-01 | Uvavanyo olu-1/ikhithi | I-Nasalpharyngeal Swab, i-Oropharyngeal Swab | Iinyanga ezingama-24 | 2-30℃ / 36-86℉ |
B005C-05 | Iimvavanyo ezi-5/ikhithi | ||||
B005C-25 | Iimvavanyo ezingama-25/ikhithi |
Nyakazisa intloko yesigulana ngasemva kwiidigri ezingama-70.Ngononophelo faka i-swab kwimpumlo de i-swab ifike ngasemva empumlweni.Shiya i-swab kwimpumlo nganye imizuzwana emi-5 ukufunxa incindi.
1. Susa ityhubhu yokukhupha kwikhithi kunye nebhokisi yokuvavanya kwisikhwama sefilimu ngokukrazula inotshi.Zibeke kwinqwelomoya ethe tye.
2. Emva kwesampulu, cwilisa i-smear ngaphantsi kwinqanaba le-liquid ye-sample extraction buffer, jikeze kwaye ucinezele amaxesha ama-5.Ixesha lokuntywila le-smear ubuncinci be-15s.
3. Susa i-swab kwaye ucinezele i-edge yetyhubhu ukuze ukhuphe ulwelo kwi-swab.Phosa iswabhu kwinkunkuma eyingozi yebhayoloji.
4. Lungisa ikhava yepipette ngokuqinileyo phezulu kwityhubhu yokufunxa.Emva koko ujike ngobunono ityhubhu yokukhupha5 amaxesha.
5. Dlulisa i-2 ukuya kwi-3 yehla (malunga ne-100 ul) yesampuli kwindawo yesampula yebhendi yokuvavanya kwaye uqale i-timer.Qaphela: ukuba iisampulu ezikhenkcezisiweyo zisetyenzisiwe, iisampuli kufuneka zibe nobushushu begumbi.
Emva kwemizuzu eyi-15, funda iziphumo ngokubonakalayo.(Qaphela: SUKUFUNDA iziphumo emva kwemizuzu engama-20!)
1.SARS-CoV-2 Iziphumo Ezincumisayo
Iibhendi ezinemibala zivela kumgca wokuvavanya zombini (T) kunye nomgca wokulawula (C).Ibonisa a
iziphumo ezilungileyo ze-SARS-CoV-2 antigens kumzekelo.
2.Isiphumo esihle seFluA
Iibhendi ezinemibala zivela kumgca wokuvavanya zombini (T1) kunye nomgca wokulawula (C).Ibonisa
isiphumo esihle kwii-antigens ze-FluA kumzekelo.
3.Isiphumo esihle seFluB
Iibhendi ezinemibala zivela kumgca wokuvavanya zombini (T2) kunye nomgca wokulawula (C).Ibonisa
isiphumo esihle kwii-antigens ze-FluB kwi-specimen.
4.Isiphumo esibi
Ibhendi enemibala ibonakala kumgca wolawulo (C) kuphela.Ibonisa ukuba
Uxinzelelo lwe-SARS-CoV-2 kunye ne-FluA/FluB antigens azikho okanye
ngaphantsi komda wokubhaqwa kovavanyo.
5.Isiphumo esingasebenziyo
Akukho bhendi enemibala ebonakalayo ibonakala kumgca wokulawula emva kokwenza uvavanyo.I
Izalathiso zinokungalandelwa ngokuchanekileyo okanye uvavanyo lunokuba nalo
iye yaba mandundu.Kucetyiswa ukuba lo mzekelo uphinde uvavanywe.
Igama lemveliso | Ikati.Hayi | Ubungakanani | Umzekelo | Beka ubomi kwishelufa | Trans.& Sto.Temp. |
I-SARS-CoV-2 kunye nomkhuhlane we-A/B Antigen Combo Rapid test kit (Lateral chromatography) | B005C-01 | Uvavanyo olu-1/ikhithi | I-Nasalpharyngeal Swab | Iinyanga ezili-18 | 2-30℃ / 36-86℉ |
B005C-05 | Iimvavanyo ezi-5/ikhithi | ||||
B005C-25 | Iimvavanyo ezingama-25/ikhithi |
Uvavanyo lwe-COVID-19/Flu A&B luvavanyo lokugobhoza kwegazi olusecaleni olulungiselelwe i-in vitro ekhawulezayo, esemgangathweni ngaxeshanye
ukubhaqwa kunye nokwahlulwa kwe-nucleocapsid antigen ukusuka kwi-SARS-CoV-2, umkhuhlane A kunye / okanye umkhuhlane B ngqo ukusuka ngaphambili.
Iimpumlo okanye i-nasopharyngeal swab specimens ezifunyenwe kubantu, abarhanelwa usulelo lwentsholongwane yokuphefumla.
Ngokuhambelana ne-COVID-19 ngumboneleli wabo wezempilo, kwisithuba seentsuku ezintlanu zokuqala kweempawu.Iimpawu zeklinikhi kunye
Iimpawu zosulelo lwentsholongwane yokuphefumla ngenxa ye-SARS-CoV-2 kunye nomkhuhlane zinokufana.Uvavanyo lulinganiselwe kwiilabhoratri
eqinisekisiweyo phantsi kweClinical Laboratory Improvement Amendments of 1988 (CLIA), 42 USC §263a, edibana ne
iimfuno zokwenza uvavanyo oluphakathi, oluphezulu, okanye oluyekiweyo lokuntsokotha.Le mveliso igunyaziswe ukuba isetyenziswe kwindawo yokuKhathalela
(POC), oko kukuthi, kwiindawo zokhathalelo lwesigulane ezisebenza phantsi kweSiqinisekiso sokuValwa kwe-CLIA, iSatifikethi sokuThotyelwa, okanye iSatifikethi se-CLIA.
Ukuvunywa.