SARS-CoV-2 Virus Antigen-Uvavanyo lwasekhaya

Inkcazelo emfutshane:

Le khithi yokuFumana yeyokufumana umgangatho we-in vitro we-antigen ye-SARS-CoV-2 kwiisampulu ze-swab yeempumlo.Olu vavanyo lujolise ekuzivavanyeni ngaphandle komyalelo wasekhaya ngokuziqokelela ngokwazo iisampulu zempumlo zangaphambili (iinares) ezivela kubantu abaneminyaka eli-15 ubudala nangaphezulu abarhanelwa ukuba bane-COVID-19 okanye abantu abadala baqokelele iisampulu zempumlo kubantu abangaphantsi kweminyaka eli-15 ubudala. abarhanelwa ukuba bane-COVID-19.

Thumela i-imeyile kuthi

Iinkcukacha zeMveliso

Iithegi zeMveliso

Igama lemveliso

HWTS-RT062IA/B/C-SARS-CoV-2 Virus Antigen Detection Kit (indlela yegolide ye-colloidal)-Nasal

Isatifikethi

CE1434

I-Epidemiology

Isifo seCoronavirus sika-2019 (COVID-19), yinyumoniya ebangelwa kukosuleleka yinoveli coronavirus ebizwa ngokuba yiSevere Acute Respiratory Syndrome Corona-Virus 2 (SARS-CoV-2).I-SARS-CoV-2 yi-coronavirus yenoveli kwi-β genus, amasuntswana agqunyiweyo angqukuva okanye ombhoxo, anobubanzi obusuka kuma-60 nm ukuya kwi-140 nm.Umntu ngokuqhelekileyo usesichengeni se-SARS-CoV-2.Eyona mithombo yosulelo zizigulana eziqinisekisiweyo ze-COVID-19 kunye nomthwali we-SARSCoV-2 ongenazimpawu.

Uphononongo lweklinikhi

Ukusebenza kwe-Antigen Detection Kit kwavavanywa kwizigulana ezingama-554 zempumlo yokucolwa kweempumlo eziqokelelwe kubarhanelwa abaneempawu ze-COVID-19 phakathi kweentsuku ezisi-7 zokuvela kweempawu xa kuthelekiswa novavanyo lwe-RT-PCR.Ukusebenza kweKhithi yoVavanyo ye-SARS-CoV-2 Ag imi ngolu hlobo lulandelayo:

SARS-CoV-2 Virus Antigen (isixhobo sophando)	RT-PCR reagent		Iyonke
SARS-CoV-2 Virus Antigen (isixhobo sophando)	Okuhle	Ibi	Iyonke
Okuhle	97	0	97
Ibi	7	450	457
Iyonke	104	450	554

Uvakalelo	93.27%	95.0% CI	86.62% - 97.25%
Ukuchaza ngokuthe ngqo	100.00%	95.0% CI	99.18% - 100.00%
Iyonke	98.74%	95.0% CI	97.41% - 99.49%

IiParameters zobuGcisa

Ubushushu bokugcina	4℃-30℃
Uhlobo lwesampuli	iisampuli swab ngeempumlo
Beka ubomi kwishelufa	Iinyanga ezingama-24
Izixhobo ezincedisayo	Ayifuneki
Izinto ezisetyenziswayo ezongezelelweyo	Ayifuneki
Ixesha lokubona	15-20 imiz
Ukuchaza ngokuthe ngqo	Akukho cross-reactivity ne pathogens ezifana Coronavirus yomntu (HCoV-OC43, HCoV-229E, HCoV-HKU1, HCoV-NL63), Novel influenza A H1N1 (2009), umkhuhlane wonyaka A (H1N1, H3N2, H5N1, H7N9) , Umkhuhlane B (Yamagata, Victoria), Intsholongwane yokuphefumla ye-syncytial virus A/B, i-Parainfluenza virus (1, 2 kunye ne-3), Rhinovirus (A, B, C), Adenovirus (1, 2, 3, 4,5, 7, 55) ).

Ukuhamba komsebenzi

1. Isampuli
●Faka ngobunono yonke incam ethambileyo yeswab (ngokuqhelekileyo i-1/2 ukuya kwi-3/4 ye-intshi) kwi-intshi enye, Ukusebenzisa uxinzelelo oluphakathi, hlikihla i-swab kuzo zonke iindonga zangaphakathi zempumlo yakho.Yenza ubuncinane izangqa ezi-5 ezikhulu.Kwaye impumlo nganye kufuneka ihlanjwe imizuzwana eyi-15. Usebenzisa iswab efanayo, phinda okufanayo kwenye impumlo yakho.

●Ukunyibilika kwesampulu.Gxuma i-swab ngokupheleleyo kwisisombululo sokutsalwa kwesampulu;Yaphula intonga ye-swab kwindawo yokuphuka, ushiye isiphelo esithambileyo kwi-tube.Screw kwi-cap, guqula amaxesha angama-10 kwaye ubeke ityhubhu kwindawo ezinzileyo.