(COVID-19) Ikhithi yokuhlola ye-IgM/IgG Antibody Rapid (Latex Chromatography)
Ukusetshenziswa Okuhlosiwe
Okokutholwa ngokushesha, okufanelekile kwe-anti-acute respiratory syndrome 2 (SARS-CoV-2) IgG/IgM yamasosha omzimba egazini lomuntu lonke, isampula ye-serum noma i-plasma.Ukuhlolwa kuzosetshenziswa njengosizo ekuhlonzweni kwesifo sokutheleleka nge-coronavirus, esidalwa yi-SARS-CoV-2.Ukuhlolwa kunikeza imiphumela yokuhlolwa yokuqala.Imiphumela engemihle ayikuvimbeli ukutheleleka kwe-SARS-CoV-2 futhi ayikwazi ukusetshenziswa njengesisekelo sodwa sokwelashwa noma esinye isinqumo sokuphatha.Ukusetshenziswa kwe-in vitro diagnostic kuphela.
Isimiso Sokuhlola
Isekelwe kumgomo wokubamba i-immunoassay ukuze kutholwe amasosha omzimba e-COVID-19 IgG/IgM egazini lomuntu lonke, i-serum ne-plasma.Lapho isampula yengezwa kudivayisi yokuhlola, isampula izomuncwa kudivayisi ngokwenza i-capillary, ihlanganiswe ne-SARS-CoV-2 recombinant antigen-color latex conjugate futhi igeleze kulwelwesi olumbozwe ngaphambili.
Okuqukethwe Okuyinhloko
Izingxenye ezinikeziwe zibalwe kuthebula.
| Ingxenye REF REF | B001C-01 | B001C-25 |
| Hlola Ikhasethi | 1 ukuhlola | 25 izivivinyo |
| Kuyalahlwa | 1 isiqephu | 25 ama-pcs |
| Isampula Lysis Isixazululo | 1 ithubhu | 25 amashubhu |
| Imiyalo Yokusetshenziswa | 1 isiqephu | 1 isiqephu |
| Isitifiketi Sokuhambisana | 1 isiqephu | 1 isiqephu |
Ukugeleza Kokusebenza
Uma i-reagent igcinwe esiqandisini ku-4-8℃, susa ikhadi le-reagent bese uilibrate ekamelweni lokushisa imizuzu engaphezu kwe-30.
1. Vula isikhwama se-aluminium foil sekhadi lokuhlola.Susa ikhadi lokuhlola bese ulibeka livundlile etafuleni.
2. Sebenzisa i-pipette ukuze ufune isampula (i-serum, i-plasma noma igazi eliphelele) bese wengeza u-10μL embobeni yesampula yekhadi lokuhlola, bese wengeza isixazululo sesampula esingu-60μL ngokushesha.Qala ukubala.
3. Ngemuva kwemizuzu eyi-15, funda imiphumela ngokubuka.(Qaphela: UNGAYIFUNDI imiphumela ngemva kwemizuzu engu-20!)
Ukuhunyushwa komphumela
1.Umphumela ongemuhle
Uma kuphela ulayini wokulawula ikhwalithi uvela futhi imigqa yokuhlonza u-G no-M ingabonisi, kusho ukuthi alikho i-anti-coronavirus yenoveli etholakele futhi umphumela uba negethivu.
2. Umphumela Omuhle
2.1 Uma kokubili ulayini wokulawula ikhwalithi C kanye nolayini wokuhlonza ongu-M kuvela, kusho ukuthi kutholwa i-antibody ye-IgM ye-coronavirus yenoveli, futhi umphumela uba positive ku-antibody ye-IgM.
2.2 Uma kokubili ulayini wokulawula ikhwalithi C kanye nolayini wokuhlonza u-G kuvela, kusho ukuthi kutholwa i-antibody ye-IgG ye-coronavirus yenoveli futhi umphumela uba positive ku-antibody ye-IgG.
2.3 Uma kokubili ulayini wokulawula ikhwalithi C kanye nemigqa yokuhlonza u-G no-M ivela, kusho ukuthi amasosha omzimba e-coronavirus IgG ne-IgM ayatholwa, futhi umphumela uba muhle kuwo womabili amasosha omzimba e-IgG ne-IgM.
3. Umphumela Ongavumelekile
Uma ulayini wokulawula ikhwalithi C ungenakubonwa, imiphumela izoba engavumelekile kungakhathaliseki ukuthi umugqa wokuhlola uyabonisa, futhi ukuhlola kufanele kuphindwe.
Oda Ulwazi
| Igama Lomkhiqizo | Ikati.Cha | Usayizi | Isifanekiso | I-Shelf Life | Trans.& Sto.Temp. |
| (COVID-19) Ikhithi yokuhlola ye-IgM/IgG Antibody Rapid (Latex Chromatography) | B001C-01 | 1 test/kit | ISerum/Plasma/Igazi Eliphelele | Izinyanga ezingu-18 | 2-30℃ / 36-86℉ |
| B001C-01 | Izivivinyo ezingama-25/ikhithi |
