FIV Ab/FeLV Ag/Heartworm Ag Combo Rapid Test Kits (FIV-FeLV-HW)

TEST PROCEDURE

- Bvumira zvinhu zvese, zvinosanganisira sampuli uye bvunzo mudziyo, udzore ku15-25 ℃ usati wamhanyisa bvunzo.
-Bvisa mudziyo wekuyedza kubva mufoil pouch woiisa yakachinjika.-Kushandisa capillary dropper kuisa 10μL yemuenzaniso wakagadzirirwa mugomba remuenzaniso "S" remuchina wekuyedza.Wodonhedza madonhwe matatu (approx. 90μL) yeassay buffer mugomba remuenzaniso pakarepo.
- Dudzira mhedzisiro mu5-10 maminetsi.Mhedzisiro mushure memaminitsi gumi inoonekwa seisina basa.

ZVIRI KUSHANDISA

Iyo FIV Ab/FeLV Ag/Heartworm Ag Combo Rapid Test ikaseti yekuyedza kuona kuvepo kwemasoja ekudzivirira chirwere anorwisa Feline Immunodeficiency antibody,Feline Leukemia Virus antigen,Heartworm Antigen muropa rekatsi.

Nguva yekuedza: 5-10 maminitsi

Company Advantage

• Kambani yedu yave kuzivikanwa sebhizimusi repamusoro-soro muChina uye isu tine akawanda akatenderwa zvikumbiro zvematendi uye macopyright esoftware, ayo anoratidza hunyanzvi hwedu hwetekinoroji uye hunyanzvi.
• Semugadziri ane hunyanzvi, isu tiri bhizinesi repamusoro-soro tekinoroji "hofori" bhizinesi, rakazvipira kupa zvigadzirwa zvemhando yepamusoro uye masevhisi kune vatengi vedu.
• Isu tinopa masevhisi eOEM kune vatengi vedu, tichivabatsira kugadzirisa zvigadzirwa zvavo uye kugadzirisa chimiro chavo chemhando.
• Kambani yedu yakawana ISO13485, CE, uye GMP zvitupa, uye isu takazvipira kugadzirira akasiyana magwaro ekutumira kuti tive nechokwadi chekuendesa zvigadzirwa zvedu zvakanaka.
• Isu tinonzwisisa kukosha kwekutaurirana nenguva nevatengi vedu, uye isu tinova nechokwadi chekupindura kumibvunzo yese mukati meawa makumi maviri nemana, tichipa mhinduro dzehunyanzvi uye dzakakwana kune zvavanoda.