Iimpawu zoMsebenzi
Umda wokufumanisa: 1.0 ng / mL;
Uluhlu lomgca: 1.0 ~ 1000.0 ng / mL;
I-coefficient yokulungelelanisa yomgca R ≥ 0.990;
Ukuchaneka: ngaphakathi kwe-batch CV ngu ≤ 15%;phakathi kweebhetshi iCV yi ≤ 20%;
Ukuchaneka: ukutenxa okunxulumene neziphumo zomlinganiselo akusayi kudlula ± 15% xa isilinganisi sokuchaneka esilungiswe ngumgangatho wesizwe weDengue okanye isilinganisi sokuchaneka esisemgangathweni sivavanywa.
1. Gcina i-detector buffer ku-2～30℃.Isithinteli sizinzile ukuya kwiinyanga ezili-18.
2. Gcina i-Aehealth Ferritin Rapid Quantitative test cassette kwi-2～30℃, ubomi beshelufu bufikelela kwiinyanga ezili-18.
3. Ikhasethi yovavanyo kufuneka isetyenziswe kwiyure enye emva kokuvula ipakethi.
Intsholongwane yeDengue feverintsholongwane emthubi, isasazwe ikakhulu kwimimandla yetropikhi kunye ne-subtropical.Idengue yeyona ibalulekileyoI-arthropod ethwele isifo sentsholongwane kwihlabathi jikelele malunga nokugula kunye nokufa kwaye kubangelwa nayiphi naye-serotypes ezine ze-virus ye-dengue (DENV- 1 ukuya kwi-4).I-DENV inokosulela iintlobo ezininzi zeeseli kunye nonobangelaiziphumo ezahlukeneyo zeklinikhi kunye ne-pathological.
I-Aehealth Dengue NS1 Ag Rapid Test isekwe kubuchwepheshe be-fluorescence immunoassay.II-Aehealth Dengue NS1 Ag Rapid Test isebenzisa isandwich immunodetection method, xa isampuluyongezwa kwisampulu yequla leCassette yovavanyo, i-fluorescence-ilebhele i-detector Dengue NS1I-antibody ye-Ag ibophelela kwiDengue NS1 Ag antigen kumzekelo wegazi.Njengoko umxube wesampulu ufudukakwi-nitrocellulose matrix yovavanyo lomtya ngesenzo se-capillary, iicomplexes ze-detector antibodykunye neDengue NS1 Ag zifakwe kwi-antibody yeDengue NS1 Ag engakwaziyo ukuhamba.uvavanyo strip.Ngoko ke okukhona i-antigen yeDengue NS1 Ag ikwisampulu yegazi, kokukhona iicomplexes zininziziqokelelwe kumcu wovavanyo.Ubunzulu bomqondiso we-fluorescence ye-antibody ye-detector ibonisa inaniIDengue NS1 Ag ibanjiwe kunye neAehealth FIA Meter ibonisa iziphumo zovavanyo lweDengue NS1 Agisampuli yegazi.