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umkhiqizo

I-KaiBiLi COVID-19 IgG / IgM

Isitifiketi se-CE

IKaiBiLiTM I-COVID-19 IgG / IgM Rapid Test Device i-lateral flow chromatographic immunoassay yokutholwa kwekhwalithi ye-IgG ne-IgM antibodies kuya ku-2019-Novel Coronavirus egazini eliphelele lomuntu, le-serum noma le-plasma.


Imininingwane yomkhiqizo

Amathegi womkhiqizo

Isingeniso

IKaiBiLiTM I-COVID-19 IgG / IgM Rapid Test Device i-lateral flow chromatographic immunoassay yokutholwa kwekhwalithi ye-IgG ne-IgM antibodies kuya ku-2019- Novel Coronavirus egazini lonke lomuntu, i-serum noma i-plasma specimen. Isetshenziswa kuphela njengenkomba yokuthola eyengeziwe yamacala amasha asolwayo wokutholwa okungalungile kwe-coronavirus nucleic acid noma ngokuhlangana nokutholwa kwe-nucleic acid ekutholeni amacala asolwayo. Ayikwazi ukusetshenziswa njengesisekelo sokuxilongwa nokukhishwa kwe-pneumonitis etheleleke nge-2019-nCoV ukutheleleka. Akufanelekile ukuhlolwa kwabantu abaningi.

Noma yisiphi isifanekiso esisebenza nge-COVID-19 IgG / IgM Rapid Test Device kufanele siqinisekiswe ngezinye izindlela zokuhlola kanye nokutholakele komtholampilo. Umphumela omuhle wokuhlolwa udinga ukuqinisekiswa okwengeziwe. Imiphumela emibi ayikuvimbeli ukutheleleka okunamandla kwe-2019-nCoV. Uma kusolwa ukutheleleka okunamandla, ukuhlolwa okuqondile kwe-antigen ye-COVID-19 kuyadingeka. Imiphumela emihle yamanga ye-COVID-19 IgG / IgM Test Rapid ingenzeka ngenxa yokuphinda-kusebenze kusuka kuma-antibodies asekhona noma ezinye izimbangela. Ngenxa yobungozi bemiphumela emihle engamanga, ukuqinisekiswa kwemiphumela emihle kufanele kubhekwe kusetshenziswa ukuhlolwa kwesibili, okuhlukile kwe-IgG noma kwe-IgM.

Ukutholwa

Idivayisi Yokuhlola Esheshayo ye-COVID-19 IgG / IgM (Igazi Lonke/I-Serum/I-Plasma) i-qualitative lateral flow immune test ye-immunechromatographic yokuthola i- IAma-antibodies e-gG ne-IgM kuya ku-2019-nCoV egazini eliphelele, le-serum noma le-plasma. 

Isifanekiso

Isivivinyo sisebenzisa i-anti-human IgM antibody (umugqa wokuhlola i-IgM), i-anti-human IgG (umugqa wokuhlola i-IgG) kanye ne-anti-rabbit IgG (umugqa wokulawula C) okhubazeke emgqeni we-nitrocellulose. 

Ukunemba

Umphumela we-IgG:

Ukuzwela Okuhlobene: 98.28%   

Imininingwane Ehlobene: 97.01%  

Ukunemba: 97.40%

Umphumela we-IgM:

Ukuzwela Okuhlobene: 82.76%  

Imininingwane Ehlobene: 98.51% 

Ukunemba: 93.75%  

Isikhathi Semiphumela

Funda imiphumela ngemizuzu engu-15 futhi ungadluli imizuzu engama-30. 

Izimo zokugcina izinto

2 ~ 30 ° C. 

Okuqukethwe

Incazelo

Inani

Amadivayisi wokuhlola we-COVID-19 antigen

Ukuhlolwa okungama-40

Isampula buffer

1 isitsha

Isilayidi sepulasitiki

40Pcs

Uku-oda Ulwazi

Umkhiqizo

Ikati Cha.

Okuqukethwe

KaiBiLiTM I-COVID-19 IgG / IgM

P231133

40 Ukuhlolwa


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