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

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

Inkcazelo emfutshane:

Intshayelelo
Le khithi isetyenziselwa kuphela ukufunyaniswa komgangatho we-in vitro ka-2019-nCoV (COVID-19) izilwa-buhlungu ze-IgM kunye ne-IgG ezivela kwiserum okanye kwiplasma yabantu.


Iinkcukacha zeMveliso

IMIFANEKISO

Khuphela

Iithegi zeMveliso

Iimeko zesicelo

Le khithi ifanelekile kuxilongo oluncedisayo luka-2019-nCoV (COVID-19).
Ukuxilongwa kweklinikhi kunye nokunyangwa kwezigulane kufuneka kuthathelwe ingqalelo kunye neempawu zabo / iimpawu, imbali yonyango, ezinye iimvavanyo zebhubhoratri kunye neempendulo zonyango.

Iingenelo

Inzuzo
I-IgM kunye ne-IgG zazikwikhadi elinye
Ukufunyanwa kwama-antibodies amabini ngexesha elinye, elingabonisa ubukho bosulelo okanye usulelo lwangaphambili, phucula ukuchaneka kokufumanisa.

Ukucaciswa okuphezulu
ixabiso le-OD elifunyenwe ngu-ELISA lalimalunga ne-0.9 ~ 1.1.Kwakungekho ukuphendula okunqamlezayo phakathi kwekiti kunye ne-96 pathogens.

Kulula ukusebenza
Umsebenzi ulula, akukho sixhobo sokukhangela esifunekayo, iziphumo zingafumaneka kwimizuzu eyi-15.

Iskimu esibalulekileyo sokuxilongwa
Njengesikimu esincedisayo soxilongo esibalulekileyo sika-2019-nCoV (COVID-19) ukufunyaniswa, ifanelekile ukuba ibonwe emva kweentsuku ezisi-7 zeempawu.

Ukusebenza

IgG
Uvakalelo: 88.68% (76.97 ~ 95.73%)
Ucalulo: 100% (95% CI: 95.85 ~ 100%)
Iyonke iyahambelana: 95.71% (95% CI: 90.91 ~ 98.41%)

IgM
Uvakalelo: 88.17% (79.82 ~ 93.94%)
Ukukhankanya: 98.34% (95.81~99.55%)
Ukuhambelana ngokupheleleyo: 95.51% (95% CI: 92.70 ~ 97.46%)

Amacandelo

Amacandelo

Ilayisha ubungakanani (Inkcazo)

1 Uvavanyo / Ikhithi

Iimvavanyo ezingama-20/Ikhithi

Iimvavanyo ezingama-50 / iKit

Ikhadi lovavanyo

1 pc

20 iipcs

50 iipcs

Isampulu yokuxutywa

ityhubhu e-1 (0.2mL)

Ibhotile e-1 (2mL/ibhotile)

1 ibhotile (6mL / ibhotile)

Inkqubo yoVavanyo

1.Ingqokelela yeesampuli zegazi.

2.Layisha i-10μL kwisampulu yequla lekhadi lovavanyo ngepipette.

3.Yongeza amathontsi ama-2 (malunga ne-80 μL) yesampulu exutyiweyo kwisampulu yequla lekhadi lovavanyo.

4.funda iziphumo ze-chromogenic kwindawo yokufumanisa phakathi kwe-15 ~ 20 imizuzu ukuqinisekisa ukusebenza kakuhle kovavanyo.

Ukutolikwa kwesiphumo

Ukutolikwa kwesiphumo

Ukuchaneka kohlalutyo

Le khithi yovavanyo ingasetyenziselwa ukubona i-2019-nCoV, intsholongwane ye-Influenza A (2009 H1N1, H1N1, H3N2, H5N1, H7N9), intsholongwane ye-Influenza B (Yamagata, Victoria) ngokukodwa.

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

Ukuchazwa kwemveliso

IKit yoVavanyo lwe-IgM/IgG Antibody (Indlela yeGolide yeColloidal)


  • Ngaphambili:
  • Okulandelayo:

  • 50T

    50T9 50T1 50T2 50T3 50T4 50T5 50T6 50T7 50T8

    Bhala umyalezo wakho apha kwaye uwuthumele kuthi