COVID Neutralizing Antibody Rapid Test Kit
COVID Antibody Test Neutralizing Antibody Rapid Test Kit
COVID-19 Antibody Test Neutralizing Ab Rapid Test ndeyekushandisa Lateral flow immunochromatographic assays yekuona SARS-COV-2 neutralizing antibody (NAb), iyo inogona kushandiswa kuona mamiriro edziviriro mushure mekutapukirwa kana kubaiwa.
PRINCIPLE
Iyo SARS-CoV-2 Neutralizing Antibody Rapid Test (COVID-19 Ab) ndeyekuona masoja ekudzivirira chirwere kuSARS-CoV-2 kana majekiseni ayo. Iyo cell surface receptor angiotensin inoshandura enzyme-2 (ACE2) yakaputirwa munharaunda yekuyedza uye iyo recombinant receptor-binding domain (RBD) yakasanganiswa neanoratidza zvidimbu. Munguva yekuyedzwa, kana paine SARS-CoV-2 neutralizing masoja ekudzivirira chirwere mumuenzaniso, yaizoita neprotein RBD-particle conjugate uye isingaite nepre-coated protein ACE2. Musanganiswa wacho unobva wasimuka uchienda kumusoro pa membrane chromatographically ne capillary action uye yaisazobatwa ne pre-coated antigen.
Iyo SARS-CoV-2 Neutralizing Antibody Rapid Test (COVID-19 Ab) ine mapuroteni RBD-akavharwa zvimedu. Iprotein ACE2 yakavharwa munharaunda yebvunzo
Feature
A. Kuongororwa ropa: serum, plasma , ropa rose uye ropa remunwe zvese zviripo.
B. Zvienzaniso zviduku zvinodiwa. Serum, plasma 10ul kana ropa rose 20ul yakakwana.
C. Rapid immunity evaluation ne 10 mins.
Zvitupa zvakatenderwa zveNeutralizing AB Antibodies nekukurumidza bvunzo
CE Yakabvumidzwa
Rondedzero chena yeChina yakatenderwa Neutralizing Antibody Rapid Tes
Test Procedure
Muverengi weZvabuda
ZVIKATAURWA
1. Iyo SARS-CoV-2 Neutralizing Antibody Rapid Test (COVID-19 Ab) ndeyekushandisa in vitro diagnostic chete. Muedzo uyu unofanirwa kushandiswa pakuona kwekutangisa masoja ekudzivirira chirwere kuSARS-CoV-2 kana majekiseni ayo muropa rakazara, serum, kana plasma.
2. Iyo SARS-CoV-2 Neutralizing Antibody Rapid Test (COVID-19 Ab) inongoratidza kuvepo kwekusarereka masoja ekudzivirira chirwere eSARS-CoV-2 mumuenzaniso uye haifanirwe kushandiswa senzira yega yenzira yekuona antibody titer.
3. Muvarwere vakapora, iyo titer yeSARS-CoV-2 isina tsigiro yemasoja ekudzivirira chirwere inogona kunge iri pamusoro pezviyero zvinoonekwa. Izvo zvakanaka zvekuongorora uku hazvigone kutorwa sechirongwa chakabudirira chekudzivirira.
4. Kuramba kuripo kana kusavapo kwemasoja ekudzivirira chirwere hakugone kushandiswa kuona kubudirira kana kukundikana kwekurapa.
5. Migumisiro inobva kuvarwere vane immunosuppressed inofanira kududzirwa nekuchenjerera.
6. Sezviyedzo zvose zvekuongorora, zvigumisiro zvose zvinofanira kududzirwa pamwe chete nedzimwe ruzivo rwekliniki runowanikwa kuna chiremba.
PRECISION
Intra-Assay
Mukati-yekumhanya chaiko kwakatemwa nekushandisa gumi neshanu replicates ezvienzaniso zviviri: isina kunaka, uye spiked RBD antibody positive (5ug/mL). Zvienzaniso zvakaonekwa zvakanaka> 99% yenguva.
Inter-Assay
Pakati pe-run precision yakatemerwa ne15 yakazvimirira assays pamienzaniso miviri yakafanana: yakaipa, uye yakanaka. Matatu matatu akasiyana eSARS-CoV-2 Neutralizing Antibody Rapid Test (COVID-19 Ab) akaedzwa achishandisa zvienzaniso izvi. Zvienzaniso zvakaonekwa zvakanaka> 99% yenguva.
CHENJERERO
1.Kushandisa in-vitro diagnostic chete.
2.Haufanire kushandisa kit kupfuura zuva rekupera.
3.Usasanganise zvikamu kubva kumakiti ane nhamba yakasiyana-siyana.
4.Dzivisa kusvibiswa kwehutachiona hwema reagents.
5.Shandisa muedzo nokukurumidza sezvinobvira mushure mekuvhura kuti udzivirire kubva kune unyoro.