Uvavanyo lweAntigen ye-Avian Virus H9

I-Avian Influenza Virus H9 Antigen Test Featured Image

Inkcazelo emfutshane:

Igama lemveliso	Uvavanyo lweAntigen ye-Avian Virus H9
Igama lebrand	Testsealabs
Place of Origin	IHangzhou Zhejiang, eTshayina
Ubungakanani	3.0mm/4.0mm
Ifomathi	Ikhasethi
Umzekelo	Iimfihlo zeCloacal Iimfihlo
Ukuchaneka	Ngaphezulu kwe-99%
Isatifikethi	CE/ISO
Ixesha lokufunda	10min
Iwaranti	Ubushushu begumbi iinyanga ezingama-24
OEM	Iyafumaneka

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Intshayelelo

I-Avian Influenza Virus H9 Antigen Test is a lateral flow immunochromatographic assay yokufumanisa umgangatho wentsholongwane ye-avian influenza H9 (AIV H9) kwi-avian larynx okanye kwi-cloaca secretions.

108916 AIV H9 Ag (7)

Izinto eziphathekayo

• IiMathiriyeli ezibonelelweyo

1.Ikhasethi yoVavanyo 2.Swab 3.Buffer 4.Package Faka 5.Indawo yokusebenzela

Inzuzo

IZIPHUMO EZICACILEYO	Ibhodi yokukhangela ihlulwe ibe yimigca emibini, kwaye umphumo ucacile kwaye kulula ukuyifunda.
KULULA	Funda ukusebenza ngomzuzu we-1 kwaye akukho sixhobo sifunekayo.
KHAWUZIBONA	Imizuzu eyi-10 ngaphandle kweziphumo, akukho mfuneko yokulinda ixesha elide.

INKQUBO YOVAVANYO:

微信图片_20240607142236

Imikhomba-ndlela yokusetyenziswa

IUKUTOLIKWA KWEZIPHUMO

-Okuhle (+):Imigca emibini enemibala ibonakala.Umgca omnye kufuneka uhlale ubonakala kumgca wolawulo (C), kwaye omnye umgca ocacileyo onemibala kufuneka uvele kwindawo yovavanyo (T).

-Engalunganga (-):Umgca wombala omnye kuphela uvela kummandla wolawulo (C), kwaye akukho mgca wembala ovela kwindawo yovavanyo (T).

-Ayisebenzi:Akukho mgca wombala uvela kummandla wolawulo (C), obonisa ukuba umphumo wokuvavanya awusebenzi.Umthamo ongonelanga wesampulu okanye ubuchule benkqubo obungachanekanga zezona zizathu zinokwenzeka zokungaphumeleli komgca wolawulo.Kule meko, funda iphakheji yokufaka ngokucophelela kwaye uvavanye kwakhona ngesixhobo esitsha sovavanyo.

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Isatifikethi sembeko

Iprofayile yekhampani

Thina, i-Hangzhou Testsea Biotechnology Co., Ltd yinkampani ekhula ngokukhawuleza yobuchwephesha bebhayoloji ekhethekileyo ekuphandeni, ekuphuhliseni, ekuveliseni nasekusasazeni iikhithi zovavanyo lwe-in-vitro diagnostic (IVD) kunye nezixhobo zonyango.
Indawo yethu yi-GMP, ISO9001, kunye ne-ISO13458 eqinisekisiweyo kwaye sinemvume ye-CE FDA.Ngoku sijonge phambili ekusebenzisaneni neenkampani zaphesheya kwezilwandle ngophuhliso olufanayo.
Sivelisa uvavanyo lokuchuma, uvavanyo lwezifo ezosulelayo, uvavanyo lokusetyenziswa kakubi kweziyobisi, uvavanyo lwentliziyo, uvavanyo lokumakisha ithumba, uvavanyo lokutya kunye nokhuseleko kunye novavanyo lwezifo zezilwanyana, ukongezelela, uphawu lwethu lwe-TESTSEALABS luye lwaziwa kakhulu kwiimarike zasekhaya naphesheya.Umgangatho ogqwesileyo kunye namaxabiso ancomekayo asenza sikwazi ukuthatha ngaphezulu kwe-50% yezabelo zasekhaya.