Kari Whakamatau Antigen SARS-CoV-2 Tere

Rapid 2019-nCoV IqG/IqM Combo Tost Cnrd ts nn •mmunoenromatOQraphy based one step in vitro tost It «d<>siQfi©d for tho fuptd Qualitative delmmlnMion of IflG nr>d IflM antitxxJios to 2019 SARSVCo coronavirus -2) i roto i te tangata somm mmA.oc whole btood Rapid 2019-nCoV IgG/IgM Combo Tost Cnrd he whakakitenga mo te COVID-19 BKpoctod infected patents bosidot nudoic nod tost e taea te whakapouri i te tika o to cieloction (ko COVID19 ranei.

KAUPAPA

Tho ”W coronnvirusos tx>lonq to tbo P puninga COVID-19 H nn acute respiratory infoctous disease Poop«o om Oonocnlly suscoptiWo I tenei wa, ko nga turoro e pangia ana e te pukapuka coronavirus i roto i te puna matua o te mfoebon.n^ywplomatic mfoefod poog cah Me noho ano he puna mfoebous i te ©p o naianei

MĀTĀPONO

Rnpxl 2019-nCoV Combo Test Card e whakamahi ana i te pnnoplo o immuno^nromotoflrap^y.Mqum ant>-human igM and kiore miti human igG Aniitxxlies nro immoeniizod on tho ntfroceHutose meentxane respectively, as two individual tost tines (igM line aM IgG bno) in the test window of the test device Te raina IgM tn the test wndew * ctoier to Ko te umple i tino whaaia e IgG itnc I te mea ko te tauira iti rawa o te taone i roto i te kiriuhi i roto i te taputapu whakamatautau IM, ko te whakahokinga 2019-nCoV tae>nant 90M conjugate ka hanga i nga huinga me nga mea motuhake.

nntibodios (IgM an

Ko te kore o te roopu tg cokxed i te matapihi whakamatautau ka tohu he hua whakamatautau ne^at/vo A bwn-

NGA MAUTANGA I TUKUA

1 Raprt 2019-nCoV IgG-lgM Kaari Whakamātautau Paheko

2 Tauira parepare

2 pL pipet capillary 4 Tohutohu mo te Whakamahi

NGĀ MAUTANGA ENGARI KAHORe i te tuku

Te karaka, te taima ranei, te tohi haumaru, te whakarite waipiro

PUTANGA

Whakaorangia te taputapu tost i te 4 ki te 30°C i roto i te putea onflinnl soalod Kaua e Froozo.
Ko te ra paunga if>dicaie
Me noho tonu te taputapu ki roto i nga putea hiri taketake kia rite ra ano mo te whakamahi.I muri i te whakatuwheratanga, me whakamahi tonu te taputapu whakamatautau.Kaua e whakamahia ano te taputapu.

WHAKAMAHI

1 Mo te ngaio in vitro diagnostic uso anake

2 Ko te hua •$ stncUy mo te tohunga hauora u$e anake tod 曲 mwooded mo te whakamahi whaiaro

3 Kaua e whakamahi i te hua i tua atu i te ra exprsbon

4 Kaua e mahia te hua ki te he te putea，$ darnaged ranei tM $«ai is txoken

5 Kia mau ki nga tauira katoa he mate hopuhopu

6 A pee i te tikanga Lat> tikanga aM tMOHaumarutanga rerengaMhnet mo te tukunga o te potemiaii/ hopuhopu.

rauemi Kia oti te mahi whakamatautau, tukuna nga tauira i muri i te werohanga i te 121P kx neke atu i te 20 min.

TE KOHI TANGATA HEI WHAKARANGA

1 Ko te serum, te plasma, te tauira toto katoa ranei me uru ki nga tikanga paerewa iatxxatory.

2 Te wera inacbvatKX) o nga tauira, ka puta pea te hemolyse me te paheketanga o te proton, me karo.

3 He pai ake te mahi o te whakamatautau ki nga tauira toto hou / serum i plasma Ki te kore e taea te whakamatautau i nga wa tonu, ka taea te rongoa serum I plasma ki te 2-8°C tae atu ki te 3 ra ki te (Wae m te whakamatautau Mo te rokiroki mo te wa roa, Ka taea te whakatio i te serum / plasma speamens i te ・20*C i roto i te 3 marama, ・70°C ranei mo te roa atu te peera A ape i nga huringa tio/whakarere.

4 Ko te konutai az>de ka taea te taapiri hei rongoa tae noa ki te 0.1% me te kore e pa ki nga hua whakamatautau.