I-COVID-19/Flu A&B Rapid Immunoassay Yokutholwa Okuqondile,
I-COVID-19/Flu A&B Immunoassay Esheshayo Yokutholwa Okuqondile,
Ukusetshenziswa Okuhlosiwe
I-SARS-CoV-2 & Influenza A/B Antigen Combo Rapid Test Kit (Lateral chromatography) izosetshenziswa ngokuhambisana nokubonakaliswa komtholampilo kanye neminye imiphumela yokuhlolwa kwaselabhorethri ukusiza ekuxilongweni kweziguli ezinezinsolo ze-SARS-CoV-2 noma zoMkhuhlane A. /B ukutheleleka.Ukuhlolwa kufanele kusetshenziswe ochwepheshe bezokwelapha kuphela.Ihlinzeka kuphela ngomphumela wokuhlolwa wokuqala futhi ezinye izindlela zokuxilonga eziqondile kufanele zenziwe ukuze kutholwe ukuqinisekiswa kokutheleleka kwe-SARS-CoV-2 noma Umkhuhlane A/B.Okokusetshenziswa kochwepheshe kuphela.
Isimiso Sokuhlola
I-SARS-CoV-2 & Influenza A/B Antigen Combo Rapid Test Kit (Lateral chromatography) iyi-lateral flow chromatographic immunoassay.Inemiphumela emibili yeWindows.Kwesokunxele ama-antigen akwa-SARS-CoV-2.Inemigqa emibili eboshwe ngaphambili, "T" Umugqa Wokuhlola kanye nomugqa "C" Wokulawula kulwelwesi lwe-nitrocellulose.Kwesokudla kunewindi lomphumela we-FluA/FluB, inemigqa emithathu eboshwe ngaphambili, ulayini we-“T1” FluA Test, “T2” FluB Test line kanye “C” Control line kulwelwesi lwe-nitrocellulose.
Igama Lomkhiqizo | Ikati.Cha | Usayizi | Isifanekiso | I-Shelf Life | Trans.& Sto.Temp. |
I-SARS-Cov-2 & Influenza A&B Antigen Rapid Test Kit(Immunochromatographic Assay) | B005C-01 | 1 test/kit | I-Nasalpharyngeal Swab, i-Oropharyngeal Swab | Izinyanga ezingama-24 | 2-30℃ / 36-86℉ |
B005C-05 | Izivivinyo ezi-5/ikhithi | ||||
B005C-25 | Izivivinyo ezingama-25/ikhithi |
Tshekisa ikhanda lesiguli emuva ngamadigri angu-70.Faka ngokucophelela i-swab ekhaleni kuze kube yilapho i-swab ifika ngemuva kwekhala.Shiya i-swab ekhaleni ngalinye imizuzwana emi-5 ukuze umunce uketshezi.
1. Khipha ishubhu lokukhipha ekhithi kanye nebhokisi lokuhlola esikhwameni sefilimu ngokuklebhula inotshi.Zibeke endizeni enezingqimba.
2. Ngemva kokuthatha isampula, cwilisa i-smear ngaphansi kwezinga loketshezi lesampula yokukhipha ibhafa, zungezisa bese ucindezela izikhathi ezi-5.Isikhathi sokucwilisa se-smear okungenani ama-15s.
3. Khipha i-swab bese ucindezela unqenqema lweshubhu ukuze ukhame uketshezi ku-swab.Phonsa i-swab kudoti oyingozi webhayoloji.
4. Lungisa ikhava ye-pipette ngokuqinile phezulu kweshubhu lokumunca.Bese uvula ngobumnene ishubhu yokukhipha izikhathi ezi-5.
5. Dlulisa amaconsi angu-2 kuya kwangu-3 (cishe u-100 ul) wesampula endaweni yesampula yebhendi yokuhlola bese uqala isibali sikhathi.Qaphela: uma amasampula afriziwe asetshenziswa, amasampula kufanele abe negumbi lokushisa.
Ngemuva kwemizuzu eyi-15, funda imiphumela ngokubuka.(Qaphela: UNGAYIFUNDI imiphumela ngemva kwemizuzu engu-20!)
1.SARS-CoV-2 Umphumela Omuhle
Amabhendi anombala avela kukho kokubili kulayini wokuhlola (T) nolayini wokulawula (C).Kubonisa a
umphumela omuhle wama-antigen e-SARS-CoV-2 esibonelweni.
2.FluA Umphumela Omuhle
Amabhendi anombala avela kukho kokubili kulayini wokuhlola (T1) nolayini wokulawula (C).Ibonisa
umphumela omuhle wama-antigen e-FluA kusampula.
3.FluB Umphumela Omuhle
Amabhendi anombala avela kukho kokubili kulayini wokuhlola (T2) nolayini wokulawula (C).Ibonisa
umphumela omuhle wama-antigen e-FluB kusampula.
4.Umphumela Ongemuhle
Ibhendi enombala ivela kulayini wokulawula (C) kuphela.Ibonisa ukuthi
ukugcwala kwama-antigen e-SARS-CoV-2 kanye ne-FluA/FluB awekho noma
ngaphansi komkhawulo wokutholwa wokuhlolwa.
5.Umphumela Ongavumelekile
Alikho ibhande elinemibala elibonakalayo elivela kulayini wokulawula ngemva kokwenza uhlolo.I
izikhombisi-ndlela kungenzeka azilandelwanga kahle noma ukuhlolwa kungenzeka kube nakho
iwohloka.Kutuswa ukuthi isifanekiso siphinde sihlolwe.
Igama Lomkhiqizo | Ikati.Cha | Usayizi | Isifanekiso | I-Shelf Life | Trans.& Sto.Temp. |
I-SARS-CoV-2 & Influenza A/B Antigen Combo Rapid test kit (Lateral chromatography) | B005C-01 | 1 test/kit | I-Nasalpharyngeal Swab | Izinyanga ezingu-18 | 2-30℃ / 36-86℉ |
B005C-05 | Izivivinyo ezi-5/ikhithi | ||||
B005C-25 | Izivivinyo ezingama-25/ikhithi |
Ukuhlolwa kwe-COVID-19/Flu A&B kuyi-lateral flow immunoassay eyenzelwe i-in vitro ngokushesha, ikhwalithi kanye kanye
ukutholwa kanye nokwehlukaniswa kwe-nucleocapsid antigen kwa-SARS-CoV-2, umkhuhlane A kanye/noma umkhuhlane B ngokuqondile kusukela ngaphambili.
izibonelo ze-swab zamakhala noma ze-nasopharyngeal ezitholwa kubantu, okusolwa ukuthi banegciwane lokuphefumula.
ngokuhambisana ne-COVID-19 ngomhlinzeki wabo wezempilo, phakathi nezinsuku ezinhlanu zokuqala kwezimpawu.Izimpawu zomtholampilo kanye
izimpawu zokutheleleka ngegciwane lokuphefumula ngenxa ye-SARS-CoV-2 kanye nomkhuhlane zingafana.Ukuhlola kunqunyelwe kulabhorethri
kuqinisekiswe ngaphansi kwe-Clinical Laboratory Improvement Amendments ka-1988 (CLIA), 42 USC §263a, ehlangabezana
izimfuneko zokwenza izivivinyo eziyinkimbinkimbi, eziphakeme, noma eziyekiwe.Lo mkhiqizo ugunyaziwe ukuthi usetshenziswe endaweni Yokunakekela
(POC), okungukuthi, ezilungiselelweni zokunakekelwa kwesiguli ezisebenza ngaphansi kwesitifiketi sokuyekelela se-CLIA, Isitifiketi Sokuthobela, noma Isitifiketi
Ukugunyazwa.