I-Diagnostic Kit (LATEX) ye-Rotavirus Group A kunye ne-adenovirus
Diagnostic Kit(LATEX)yeRotavirus IQela A kunye ne-adenovirus
Ukusetyenziswa kwe-in vitro diagnostic kuphela
Nceda ufunde le phakheji ifake ngononophelo phambi kokuba uyisebenzise kwaye ulandele ngokungqongqo imiyalelo. Ukuthembeka kweziphumo zovavanyo akunakuqinisekiswa ukuba kukho nakuphi na ukutenxa kwimiyalelo ekweli phakheji.
UKUSETYENZISWA OKUHLOSIWEYO
I-Diagnostic Kit (i-LATEX) ye-Rotavirus yeQela A kunye ne-adenovirus ifanelekile ukubhaqwa kwekhwalithi ye-Rotavirus yeQela A kunye ne-adenovirus antigen kwiisampuli ze-fecal yabantu. Olu vavanyo lujoliswe ekusetyenzisweni kwiingcali zempilo kuphela.Ngeli xesha, olu vavanyo lusetyenziselwa ukuxilongwa kwekliniki yorhudo olusanda kuzalwa kwizigulane ezine-Rotavirus Group Agroup A.i-rotaviruskunye nosulelo lwe-adenovirus.
UBUKHULU BOKUPACKAGE
Ikhithi eyi-1 / ibhokisi, iikiti ezili-10 / ibhokisi, iikiti ezingama-25,/ibhokisi, iikiti ezingama-50 / ibhokisi
USHWANKATHELO
I-Rotavirus ihlelwa njengei-rotavirusuhlobo lwentsholongwane ye-exenteral, enemilo engqukuva enobubanzi obumalunga ne-70nm. I-Rotavirus iqulethe i-11 yamacandelo e-RNA ephindwe kabini. I-rotavirus ingaba ngamaqela asixhenxe (ag) ngokusekelwe kwiiyantlukwano ze-antigenic kunye neempawu zofuzo. Usulelo lwabantu lweqela A, iqela B kunye neqela le-rotavirus lixeliwe I-Rotavirus Iqela A ngunobangela obalulekileyo we-gastroenteritis enzima ebantwaneni kwihlabathi jikelele.[1-2]. I-adenoviruses yabantu (HAdVs) ine-51 serotypes, enokuthi ibe yi-6 subtypes (A~F) ngokusekelwe kwi-immunology kunye ne-biochemistry.[3]. I-Adenoviruses inokosulela ukuphefumla, amathumbu, iliso, isinyi, kunye nesibindi, kwaye ibangele ukusasazeka kwesifo. Abantu abane-immunity eqhelekileyo bahlala bevelisa izilwa-buhlungu kwaye baziphilise ngokwabo. Kwizigulane okanye kubantwana abakhuselekanga kuthintelo, usulelo lwe-adenovirus lunokubulala.
INKQUBO YOVAVANYO
1.Thatha intonga yesampulu, uyifake kwisampulu yelindle, emva koko ubeke intonga yesampulu ngasemva, jija uqinise kakuhle, phinda intshukumo ka-3. Okanye usebenzisa intonga yesampulu ichola malunga ne-50mg yesampuli yelindle, kwaye ufake kwityhubhu yesampulu yelindle equlethe isampulu yedilution, kwaye ujije ngokuqinileyo.
2.Sebenzisa isampulu yepipette elahlwayo thatha isampuli yelindle elibhityileyo kwisigulana sorhudo, emva koko wongeze amathontsi ama-3 (malunga ne-100uL) kwityhubhu yesampulu ye-fecal kwaye uvuthulule kakuhle, ubeke ecaleni.
3.Khupha ikhadi lovavanyo kwibhegi yefoyile, uyibeke kwitafile yenqanaba kwaye uyiphawule.
4.Susa i-cap kwi-tube yesampuli kwaye ulahle i-drops yokuqala ye-diluted samples, yongeza i-3 yehla (malunga ne-100uL) akukho bubble diluted isampuli ngokuthe nkqo kwaye ngokukhawuleza kwisampuli kakuhle yekhadi kunye ne-dispette enikeziweyo, qalisa ixesha.
5.Isiphumo kufuneka sifundwe kwimizuzu eyi-10-15, kwaye ayisebenzi emva kwemizuzu eyi-15.