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I-2019-nCoV IgM/IgG Antibody Test Kit (indlela yegolide ye-colloidal)

I-2019-nCoV IgM/IgG Antibody Test Kit (indlela yegolide ye-colloidal)

Incazelo emfushane:

Isingeniso
Le kit isetshenziselwa kuphela ukutholwa kwekhwalithi ye-in vitro ye-2019-nCoV (COVID-19) IgM kanye ne-IgG yamasosha omzimba avela ku-serum yomuntu noma i-plasma.


Imininingwane Yomkhiqizo

IZITHOMBE

Landa

Omaka bomkhiqizo

Izimo zohlelo lokusebenza

Le khithi ifanele ukuhlonzwa okuwusizo kwe-2019-nCoV (COVID-19).
Ukuxilongwa nokwelashwa kweziguli kufanele kucatshangelwe kuhlanganiswe nezimpawu/izimpawu zazo, umlando wezokwelapha, okunye ukuhlolwa kwaselabhorethri kanye nezimpendulo zokwelashwa.

Izinzuzo

Inzuzo
I-IgM ne-IgG zazisekhadini elifanayo
Ukutholwa kwamasosha omzimba amabili ngesikhathi esisodwa, okungakhombisa ubukhona bokutheleleka noma ukutheleleka kwangaphambilini, kuthuthukisa ukunemba kokutholwa.

Ukucaciswa okuphezulu
inani le-OD elitholwe yi-ELISA lalicishe libe ngu-0.9~1.1.Kwakungekho ukusabela okuphambene phakathi kwekhithi kanye namagciwane angama-96.

Ukusebenza okulula
Ukusebenza kulula, akukho ukutholwa kwensimbi edingekayo, imiphumela ingatholakala kungakapheli imizuzu eyi-15.

Uhlelo olubalulekile lokuxilonga olusizayo
Njengohlelo olusizayo olubalulekile lokuxilonga lokutholwa kwe-2019-nCoV (COVID-19), ifanele ukutholwa ngemva kwezinsuku eziyi-7 zezimpawu.

Ukusebenza

IgG
Ukuzwela: 88.68% (76.97~95.73%)
Ukucaciswa: 100% (95%CI: 95.85~100%)
Ukungaguquguquki okuphelele: 95.71% (95%CI: 90.91~98.41%)

IgM
Ukuzwela: 88.17% (79.82~93.94%)
Ukucaciswa: 98.34% (95.81~99.55%)
Ukungaguquguquki okuphelele: 95.51% (95%CI: 92.70~97.46%)

Izingxenye

Izingxenye

Ilayisha ubuningi (Ukucaciswa)

1 Isivivinyo/Ikhithi

Izivivinyo/Ikhithi engama-20

50 Ukuhlolwa/Ikhithi

Ikhadi lokuhlola

1 pc

20 ama-pcs

50 ama-pcs

I-diluent yesampula

Ishubhu eli-1 (0.2mL)

Ibhodlela elingu-1 (2mL/ibhodlela)

Ibhodlela elingu-1 (6mL/ibhodlela)

Inqubo Yokuhlola

1.Iqoqo lesampula legazi.

2.Layisha i-10μL emthonjeni wesampula wekhadi lokuhlola nge-pipette.

3.Engeza amaconsi angu-2 (cishe ama-80 μL) esampula encibilikisiwe emthonjeni wesampula wekhadi lokuhlola.

4.funda imiphumela ye-chromogenic endaweni yokuthola phakathi kwemizuzu eyi-15 ~ 20 ukuze uqinisekise ukusebenza kahle kokuhlolwa.

Ukuhunyushwa komphumela

Ukuhunyushwa komphumela

Ukucaciswa kokuhlaziya

Le khithi yokuhlola ingasetshenziswa ukuthola i-2019-nCoV, igciwane loMkhuhlane A (2009 H1N1, H1N1,H3N2,H5N1, H7N9), igciwane Lomkhuhlane B (Yamagata, Victoria) ngokuqondile.

I-2019-nCoV-IAV-IBV Nucleic Acid Test Kit (PCR- fluorescence probe method) CE证_Page2
I-2019-nCoV-IAV-IBV Nucleic Acid Test Kit (PCR- fluorescence probe method) CE证_Page1
I-IVDD DOC 2019-nCoV IAV IBV Nucleic Acid

Ukucaciswa komkhiqizo

Ikhithi Yokuhlola I-IgM/IgG Antibody (Indlela Yegolide Ye-Colloidal)


  • Okwedlule:
  • Olandelayo:

  • 50T

    50t9 50T1 50T2 50T3 50T4 50T5 50T6 50t7 50T8

    Bhala umyalezo wakho lapha futhi usithumelele wona