Isivivinyo se-Rapid 2019-ncov coronavirus Antigen

Incazelo emfushane:

Isetshenziselwe i- Ukuhlolwa kwe-coronavirus ka-2019
Isibonelo I-Nasal Swab noma i-Swava Swab
Isitifiketi I-CE / ISO13485 / Uhlu Olumhlophe / Bhalisa ku-DE
MOQ Amakhithi wokuhlola ayi-10000
Isikhathi sokuthumela Isonto eli-1 ngemuva kokuthola inkokhelo
Ukupakisha 1 ikhithi yokuhlola / ibhokisi lokupakisha
Idatha Yokuhlola Ukuzwela nokucaciswa okungaphezu kwama-95%
I-Shelf Life iminyaka engu-2
Amandla Wokukhiqiza 1 Million / Isonto
Inkokhelo I-T / T, i-Western Union, i-Paypal

Imininingwane yomkhiqizo

Amathegi womkhiqizo

Ikhithi yokuhlola ye-IMMUNOBIO Rapid coronavirus Antigen iyindlela yokuthola esheshayo ye-antigen ye-COVID-19. I-anti-2019-ncov monoclonal antibody ibifakwe emgqeni wokuhlola futhi yahlanganiswa negolide le-colloidal. Ngesikhathi sokuhlolwa, isampula liphendule nge-anti-2019-ncov antibody conjugate emgqeni wokuhlola. Ingxube yabe isikhuphula ulwelwesi ngesenzo se-capillary futhi yasabela ngenye i-anti-2019-ncov monoclonal antibody evela endaweni yokuhlola.

Ikhithi yokuhlola ye-IMMUNOBIO Antigen isivivinyo esisheshayo sokutholakala kwekhwalithi yama-antigen ku-coronavirus yenoveli i-SARS-CoV-2 emphinjeni womuntu nasezimpumulweni zamakhala. Ukusetshenziswa kokuxilonga kwe-in vitro kochwepheshe kuphela

IZIMPAWU ZOKUSEBENZA

1. Ukuzwela, Ukucaciswa kanye nokunemba I-SARS-CoV-2 Antigen Rapid Test (i-COVID-19 Ag) iqhathaniswe ne-reagent standard standard yegolide (PCR). Umphumela ukhombise ukuzwela okuhlobene nokucaciswa

Indlela Igolide ejwayelekile reagent (PCR) Imiphumela Yonke
Ukuhlolwa kwe-SARS-CoV-2 Antigen Rapid (COVID-19 Ag) Imiphumela Oqondile Okubi
Oqondile 87 0 87
Okubi 4 300 304
Umphumela Ophelele 60 300 391

 

Ukuzwela Okuhlobene: 95.60% (95% CI: 88.89% ~ 98.63%)

Okucacile Okuhlobene: 100% (95% CI: 98.78% ~ 100.00%)

Ukunemba: 98.98% (95% CI: 97.30% ~ 99.70%)

2. Umkhawulo Wokuthola (LOD)

Umkhawulo wokutholwa kwe-SARS-CoV-2 Antigen Rapid Test (COVID-19 Ag) usufundisiwe. I-LOD yokuhlolwa kweprotheni le-SARS-CoV-2 N icishe ibe ngu-0.2-0.5ng / mL. I-LOD yesivivinyo kwigciwane le-SARS-CoV-2 (engasebenzi) icishe ibe ngu-2-5X102 TCID50/ ml

Ukuhlushwa Okuhle / Umphumela Isilinganiso Sesivumelwano
0.5ng / mL N amaprotheni 100/100 100%
5X102 TCID50/ ml 100/100 100%

3. Ukusebenza okuphambene nalokho:

I-SARS-CoV-2 Antigen Rapid Test (i-COVID-19 Ag) ihlotshaniswa nephaneli lamaprotheni amanye ama-antigen angama-coronavirus recombinant antigen nezinye izimpawu zokuphefumula igciwane elihlobene. Imiphumela ikhonjiswe eshidini elingezansi:

Into Ukuhlushwa Umphumela
Amaprotheni e-SARS-CoV-2 N 0.001μg / ml okuhle
Amaprotheni e-SARS-CoV N 1μg / ml okungekuhle
Amaprotheni e-MERS-CoV N 1μg / ml okungekuhle
HCoV-NL63 N amaprotheni 1μg / ml okungekuhle
HCoV-229E N amaprotheni 1μg / ml okungekuhle
HCoV-HKU1 N amaprotheni 1μg / ml okungekuhle
Igciwane le-Parainfluenza 1X105TCID50/ ml okungekuhle
Umkhuhlane Igciwane 1X105TCID50/ ml okungekuhle
Igciwane lomkhuhlane B 1X105TCID50/ ml okungekuhle
I-Chlamydia pneumoniae 1X105TCID50/ ml okungekuhle
I-Adenovirus 1X105TCID50/ ml okungekuhle
I-Mycoplasma pneumoniae 1X105TCID50/ ml okungekuhle
i-Respiratory syncytial virus 1X105TCID50/ ml okungekuhle

Izinto Eziphazamisayo:

Lezi zinhlanganisela ezilandelayo zihlolwe kusetshenziswa i-SARS-CoV-2 Antigen Rapid Test (COVID-19 Ag) futhi akukho ukuphazamiseka okubonwe.

Into

Ukuhlushwa

Umphumela

I-Alpha-interferon

3millionIU

Akukho ukuphazamiseka

Umucu ohlanziwe

1000ng / Ml

Akukho ukuphazamiseka

Kugunyaziwe izitifiketi

1. CE / ISO13485 / Uhlu Olumhlophe

2. Ibhaliswe eJalimane Ministry of Health

Rapid-2019-ncov-coronavirus-Antigen-test

INQUBO YOKUHLOLA

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