Semi-quantitative Covid 19 Neutraliazing antibody Rapid Test
Iimpawu zeekhithi zoVavanyo lwe-COVID Antibody Neutraliazing AB Rapid Test
A. Uvavanyo lwegazi, igazi elipheleleyo lomnwe linokwenzeka.
B. Ukufunyaniswa koMda: Ukucuthwa:100ng/ml, Uluhlu lokuFumana:50~5000ng/ml
C. Iisampulu ezincinci ziyafuneka. I-Serum, i-plasma 10ul okanye igazi elipheleleyo i-20ul yanele.
Iimpawu zetekhnoloji yokufumanisa ngokukhawuleza kwigolide ye-colloidal
1. Ukusebenza ngokufanelekileyo: amanyathelo okusebenza ayisampuli, akukho zixhobo zikhethekileyo ezifunekayo, isampuli ayifuni inkqubo ekhethekileyo, iziphumo zovavanyo zinokutolikwa ngokuthe ngqo ngeso lenyama, kwaye akukho mfuneko yezakhono ezizodwa kumqhubi.
2. Ngokukhawuleza kwaye ngokukhawuleza: kuphela i-10-15 mins iya kuvelisa iziphumo. Ngelixa ezinye iindlela ezifana ne-ELISA zifuna iiyure ezi-1-2, i-PCR ithatha ixesha elide.
3. Ukuchaneka okunamandla: ngenxa yokuba iteknoloji ibhalwe ubukhulu becala nge-monoclonal anyibodies, inqume ukuba ifumanisa kuphela i-antigenic determinant ethile, ngoko ineenkcukacha ezilungileyo kakhulu.
4. Uvakalelo luchanekile
5. Ilungele ukuthwala: ekubeni iprotheni yegolide ye-colloidal yokubhala yinkqubo yokubopha ngokomzimba, ukubopha kuqinile kwaye kunqabile ukuba kubangele utshintsho kwiprotheni. Ke ngoko, i-reagent izinzile kwaye ayichatshazelwa zizinto zangaphandle ezifana nobushushu. Inokuthwalwa kunye nawe ukuze ibekwe iliso nangaliphi na ixesha.
6. Ukhuseleko kunye nokukhuselwa kwendalo: Xa kuthelekiswa nezinye iindlela zokubona, iteknoloji ye-immune colloidal gold iwenza lula umsebenzi. Akukho zinto ezinobungozi ezifana ne-radioisotopes kunye ne-o-phenylenediamine ezibandakanyekayo kuvavanyo, ngoko ke akuyi kulimaza impilo yomsebenzi okanye kungcolise indalo. , Inokhuseleko olungenakuthelekiswa neendlela zokufumanisa ezifana ne-radioisotope okanye ileyibhile ye-enzyme.
Iziqinisekiso ezigunyazisiweyo zovavanyo olukhawulezayo lwe-Antibodies ze-AB ze-Neutralizing
CE Ivunyiwe
Uluhlu olumhlophe lwaseTshayina luvunyiwe kwi-Neutralizing Antibody Rapid Test
Inkqubo yoVavanyo
Umfundi wesiphumo
Ulawulo lwemeko
Ulawulo lweprogram yangaphakathi lufakiwe kuvavanyo. Imigca enemibala ebonakala kwindawo yolawulo (C) lulawulo lweprogram yangaphakathi. Iqinisekisa umthamo owaneleyo wesampuli kunye nobuchule benkqubo obuchanekileyo.
Le khithi ayiboneleli ngemigangatho yolawulo; nangona kunjalo, kucetyiswa ukuba ulawulo olulungileyo kunye nolungalunganga luvavanywe njengenkqubo efanelekileyo zelabhoratri yokuqinisekisa inkqubo yovavanyo kunye nokuqinisekisa ukusebenza kovavanyo olufanelekileyo.
Iimpawu zokusebenza
Uvakalelo olunxulumeneyo, Ukuchaneka nokuChaneka
UVavanyo oluKhawulezayo lwe-SARS-CoV-2 Neutralizing Antibody Rapid (COVID-19 Ab) luvavanyiwe kunye nemizekelo efunyenwe kuluntu lwesampulu eqinisekileyo nengalunganga. Iziphumo zaqinisekiswa yi-SARS-CoV-2 Neutralization Antibody Detection Kit (ELISA kit, cutoff 30% signal inhibition).
Indlela | Ikhithi yentengiso ye-SARS-CoV-2 ye-Neutralization Antibody Detection (ikhithi ye-ELISA) | Zizonke iziphumo | ||
Uvavanyo oluKhawulezayo lwe-SARS-CoV-2 lwe-Antibody oluKhawulezayo (COVID-19 Ab) | Iziphumo | Okuhle | Ibi | |
Okuhle | 32 | 0 | 32 | |
Ibi | 1 | 167 | 168 | |
Isiphumo sisonke | 33 | 167 | 200 |
Uvakalelo olunxulumeneyo: 96.97%(95%CI:83.35%~99.99%)
Iinkcukacha Ngokuhambelana: 100.00%(95%CI:97.29%~100.00%)
Ukuchaneka: 99.50%(95%CI:96.94%~99.99%)
Uvavanyo oluKhawulezayo lwe-IMMUNOBIO Neutraliazing antibody semi-quantitative Rapid luvavanyo olukhawulezayo lokuchongwa kwee-antibodies ezingathathi hlangothi kwi-SARS-CoV-2 okanye izitofu zayo zokugonya egazini, kwiserum, okanye kwiplasma.
Iziphumo ukuba uphethe ugonyo lwe-COVID-19 kulindeleke ukuba zibenje ngasezantsi.
- Phambi kwedosi yokuqala: Unegative ngovavanyo olukhawulezayo
- Iiveki ezi-3 emva kwedosi yokuqala: buthathaka okanye phakathi kakuhle
- Iveki e-1 emva kwedosi yesibini: phakathi okanye ephezulu ine-positive
- iiveki ezi-2 emva kwedosi yesibini: phakathi okanye ephezulu ine-positive