Testsealabs Malaria Ag Pf/Pv/Pan Combo Test

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Uvavanyo lweMalaria Ag Pf/Pv/Pan Combo luvavanyo olukhawulezayo lwe-chromatographic immunoassay yokufunyaniswa komgangatho we-plasmodium falciparum histidine etyebileyo yeprotein-II (pf HRP-II) , plasmodium vivax (pv LDH) kunye neplasmodium lactate dehydrogenase (pLDH) kwigazi elipheleleyo.
gouIziphumo eziKhawulezayo: ILab-Chanekile kwiMizuzu gouUkuchaneka kweBanga leLebhu: ethembekileyo kwaye ethembekileyo
gouVavanya naphi na: Akukho tyelelo lwaseLab olufunekayo  gouUmgangatho oqinisekisiweyo: 13485, CE, iMdsap iyahambelana
gouIlula kwaye iSetyenzisiwe: Kulula ukuyisebenzisa, iZero Hassle  gouULulelo olugqibeleleyo: Vavanya ngokukhululeka ekhaya

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IMalaria Ag Pf/Pv/Pan Combo Test
UVavanyo lweMalaria Ag Pf/Pv/Pan Combo luvavanyo olukhawulezayo, olusemgangathweni, lwechromatographic immunoassay eyenzelwe ukubhaqwa kunye nokwahlula ngaxeshanye.I-Plasmodium falciparum(Pf),I-Plasmodium vivax(Pv), kunye ne-pan-malarial antigens kwigazi elipheleleyo lomntu, i-serum, okanye i-plasma. Olu vavanyo lusebenzisa iteknoloji ehamba phambili ye-lateral flow ukuchonga i-antigens ethile ye-malaria-kubandakanywaP. falciparum-i-HRP-II ethile,P. vivax-i-LDH ethile, kunye ne-pan-species antigens egciniweyo (i-aldolase okanye i-pLDH) -ukubonelela ngeprofayili yokuxilonga ebanzi ngaphakathi kwemizuzu eyi-15. Yenza ukuba abaqeqeshi bezempilo bakwazi ukwahlula ngokuchanekileyo phakathiP. falciparum,P. vivax, kunye nezinyeiPlasmodiumiintlobo (umz.,P. ovale,P. malariae, okanyeP. knowlesi) kwinkqubo yovavanyo olunye. Ngobuntununtunu obuphezulu kunye nokuchaneka, olu vavanyo lusebenza njengesixhobo esiphambili esiphambili sokuxilongwa kwangoko kosulelo lwemalariya ebukhali, ukukhokela iindlela zonyango ezikhethekileyo zeentlobo, uphononongo lwe-epidemiological, kunye nolawulo lwesigulane kwiindawo ezihlala zihleli kunye nezingapheleliyo.

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