Rapid SARS-CoV-2 Antigen Test Card

Tsanangudzo Pfupi

  1. Mhedzisiro mumaminitsi gumi
  2. Huro/Nasal swabs inogona kushandiswa
  3. Yakanyanya kujeka, zvinoreva kuti yakanaka antigen bvunzo mhedzisiro inogona kunzi ndeyechokwadi
  4. Inokurumidza uye isingadhuri pane bvunzo dzema molecular

Product Detail

Product Tags

Rapid 2019-nCoV IqG/IqM Combo Tost Cnrd ts nn •mmunoenromatOQraphy yakavakirwa nhanho imwe in vitro tost It «d<>siQfi©d for tho fuptd Qualitative delmmlnMion of IflG nr>d IflM antitxxJios to 20201RS novel coronavirus -2) mumunhu somm mmA. oc yakazara btood Rapid 2019-nCoV IgG/IgM Combo Tost Cnrd ndeye supplomont yekuona yeCCIDID-19 BKpoctod infectod patents bosidot nudoic nod tost iyo inogona kushungurudza iko kurongeka kweiyo cieloction (kana COVID19

SUMMARY

Kana ”W coronnvirusos tx> lonq to Tbo P genus COVID-19 H nn acute breathing infoctoous disease Poop«o om Oonocnlly suscoptiWo Parizvino, kune varwere vakatapukirwa nenovel coronavirus uye kubva kune main source kubva kumfoebon. n^ywplomatic mfoefod poog cah Ivawo mfoebous sosi pane yazvino ©p

PRINCIPLE

Rnpxl 2019-nCoV Combo Test Card inoshandisa pnnoplo ye immuno^nromotoflrap^y. Mqum ant>-igM yemunhu uye mbeva miti yemunhu igG Aniitxxlies nro immoeniizod pane tho ntfroceHutose meentxane zvichiteerana, sematanho maviri ega ega (igM mutsara am IgG bno) muhwindo rekuyedza remuchina wekuyedza Iyo IgM mutsara tn bvunzo wndew * ctoier iyo yakasarudzika yakashongedzwa neIgG itnc Seimwe diki sampuli ftown kuburikidza ne membrane mukati meIM bvunzo mudziyo iyo ine mavara 2019-nCoV recomt> nant 90M conjugate mafomu macompexes ane chaiwo.

nntibodios (IgM an

Kusavapo kwe tg cokxed band pahwindo rebvunzo kunoratidza kuti ne^at/vo test result A bwn-

ZVINHU ZVINOPIWA

1 Raprt 2019-nCoV IgG-lgM Combo Test Card

2 Sample buffer

2 pL capillary pipet 4 Mirayiridzo Yekushandisa

ZVINHU ZVINODIWA ASI HAZVIPIWE

Wachi kana timer, chengetedzo lancets, doro prep

STORAGE

Chengetedza mudziyo wetost pa4 kusvika 30°C muhomwe yeonflinnl soalod Usa Froozo.
The expirabon date if>dicaie
Iyo ingangoita mudziyo unofanirwa kuramba uri muhomwe yepakutanga yakavharwa kusvika yagadzirira kushandiswa. Mushure mekuvhura, tho bvunzo mudziyo unofanirwa kushandiswa nekukurumidza. Usashandise zvakare mudziyo.

ZVEKUNGWARIRIRA

1 Yehunyanzvi in ​​vitro diagnostic uso chete

2 Chigadzirwa •$ stncUy for medical professional u$e only tod 曲 mwoded for personal use

3 Usashandise chigadzirwa kupfuura zuva reexprsbon

4 Usaite chigadzirwa kana homwe, $ darnaged kana tM $«ai yakazununguka

5 Bata zvienzaniso zvese zvinogona kutapukira

6 Tevedzera zvakajairwa Lat> maitiro aM tMOsafety fluxMhnet yekurasa potemiaii/ utachiona

zvinhu Kana iyo assay proceduro yapera, bvisa & e sampuli mushure me autoclaving pa121P kx ingangoita 20 min yekurapa ne0 5% Sodium HypochJonte f

SPECIMEN COLLECTION ANO GADZIRIRA

1 Iyo serum, plasma kana sampuli yeropa rose inofanirwa kuve coliedod uruSer standard iatxxatory conditions.

2 Kupisa kunacbvatKX) kwezvienzaniso, izvo zvinogona kukonzera hemolyse uye proton denaturation, zvinofanirwa kudzivirirwa.

3 Muedzo unoshanda zvakanyanya pamasampuli eropa rakazara / serum i plasma Kana kuyedzwa kusingagone kuitwa nekukurumidza, serum I plasma inogona kuchengetwa pa 2-8 ° C kusvika kumazuva matatu kana (Nzira yekuyedza Yekuchengetedza kwenguva refu, Serum / plasma speamens inogona kuomeswa nechando pa ・ 20*C lor 3 months kana ・ 70°C tef refu penod Dzivisa kudzokororwa kwefreezjng/thavwng cycles.

4 Sodium az>de inogona kuwedzerwa sekuchengetedza kusvika 0.1% pasina kukanganisa mhinduro dzebvunzo.

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