I-SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) Yokuzihlola

I-SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) yokuzihlola ihloselwe ukutholwa kwekhwalithi ye-SARS-CoV-2 Antigen (i-Nucleocapsid protein) kumasampula amathe omuntu ku-vitro.

Ezisetshenziswa kulezi zimo ezilandelayo:

1. ukuhlolwa kwabantu abaningi, njengesibhedlela, isikhumulo sezindiza, isiteshi, umphakathi, njll.

2. ukugadwa okuqhubekayo kwesikhathi esifushane.

* Isifanekiso se-anterior nasal swab, asivaleli

* Kulula kakhulu ukusebenzisa

* Elula, akukho thuluzi elidingekayo

* Ngokushesha, imiphumela phakathi nemizuzu eyi-15 ~ 20

*Iyonga izindleko

I-SARS-CoV-2 virus particle yenziwe izingxenye ezinhlanu: uchungechunge lofuzo lwe-RNA namaprotheni amane. Ungqimba olungaphandle lwezinhlayiyana yi-Spike Protein (S), kanti Imvilophu yegciwane ngaphansi kwe-Spike yenziwe nge-Envelope Protein (E) kanye ne-Membrane Protein (M). Umnyombo oqukethwe ngaphakathi kwemvilophu yisakhiwo esigoqiwe se-helical esakhiwe ngamaketanga ofuzo we-RNA kanye namaprotheni e-Nucleocapsid (N). Kusetshenziswa umgomo wokubopha okuthile kwe-antigen kanye ne-antibody, ukuba khona kwe-SARS-CoV-2 antigen(iphrotheni ye-Nucleocapsid) kungatholwa yi-antibody.

Izinzuzo ngaphezu kuka-Elisa kanye ne-PCR

Ukusebenza kwe-SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) kwasungulwa nezifanekiso ezingaba ngu-859 okungenzeka ukuthi zaqoqwa ezigulini ezinezimpawu ezisolakala ukuthi zine-COVID-19. Izibonelo ze-swab zamakhala zangaphambili zaqoqwa futhi zahlolwa ngokuvumelana nezidingo zeMiyalelo Yokusetshenziswa. Ukugcinwa, ukuthuthwa nokutholwa kwamasampuli ngemva kokuqoqwa kuhlangabezane nezidingo ezifanele zeMiyalelo Yokusetshenziswa. Ngasikhathi sinye, i-SARS-CoV-2 itholwe yi-reagent yokutholwa kwe-nucleic acid ephuthumayo.

Isifinyezo sokusebenza komtholampilo se-WIZ'S SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

I-PPA: 95.91% (C.I. 93.25%~97.55%)

I-NPA: 100.00% (C.I. 99.26%~100.00%)

I-OPA: 98.37% (C.I. 97.28%~99.03%)

Thina, umkhiqizi, kulokhu, simemezela ukuthi umkhiqizo(imikhiqizo) njengoba icaciswe ngenhla ihlangabezana nezinhlinzeko ezisebenzayo ze-European Directive 98/79/EC ku-in vitro Diagnostic Medical Devices. Wonke amadokhumenti obuchwepheshe asekelayo abonisa ukuthobela agcinwa umkhiqizi futhi angenziwa atholakale Ngummeli Ogunyaziwe wase-Europe.

Isitifiketi Senkampani

Iphrofayela Yenkampani

Inkampani Exhibition

A:Kokubili.Sibe kulo mkhakha iminyaka engaphezu kuka-7. Ngemikhiqizo yekhwalithi ephezulu kanye nenani elincintisanayo, sithemba ngobuqotho ukuthuthukisa ibhizinisi elizuzisa kakhulu namakhasimende ethu emhlabeni wonke.

A: T/T,L/C,D/A,D/P nokunye.

A: EXW, FOB, CFR, CIF, DDU njalonjalo.

A: Ngokuvamile, kuzothatha izinsuku ezingu-15 kuya kwezingu-30 ngemva kokuthola idiphozi Isikhathi esithile sokulethwa sincike ezintweni kanye nenani le-oda lakho.

A: Yebo, singakhiqiza ngamasampula akho noma imidwebo yobuchwepheshe.

IMP: Uma inani lilincane, amasampula azoba mahhala, kodwa amakhasimende kufanele akhokhe izindleko ze-courier.

A: Yebo, sinesivivinyo esingu-100% ngaphambi kokulethwa.

A: Sigcina ikhwalithi enhle kanye nentengo yokuncintisana ukuze siqinisekise ukuthi amakhasimende ethu ayazuza; futhi sihlonipha wonke amakhasimende njengomngane wethu futhi senza ibhizinisi ngobuqotho futhi senze ubungane nawo.