Multiplex-waqtiga dhabta ah PCR |Farsamada qalooca dhalaalaysa |Sax ah |Nidaamka UNG |Dareere & lyophilized reagent
Xirmadan waxa loo istcimaalaa ogaanshaha tayada ee vitro ee Plasmodium nucleic acid ee muunadaha dhiiga ee durugsan ee bukaanada looga shakisan yahay caabuqa Plasmodium.
Qalabkani wuxuu ku habboon yahay in lagu ogaado tayada Ureaplasma urealyticum (UU) ee kaadi mareenka ragga iyo shaybaarada dheecaanka xubinta taranka haweenka ee vitro.
Qalabkan waxa loo isticmaalaa ogaanshaha hidde-sideyaasha fayraska cagaarshow C (HCV) nooc-hoosaadka 1b, 2a, 3a, 3b iyo 6a ee muunadaha serum/balaasmaha ee fayraska cagaarshow C (HCV).Waxay caawisaa ogaanshaha iyo daawaynta bukaanka HCV.
Qalabkan waxaa loo isticmaalaa in lagu ogaado tayada adenovirus nucleic acid ee saxarada saxarada ee vitro.
Xirmadan waxa loo isticmaalaa in lagu ogaado teeb-tayada tayada leh ee denguevirus (DENV) nucleic acid ee laga shakisan yahay muunadda serum ee bukaanka si ay u caawiso ogaanshaha bukaanka qaba qandhada Dengue.
Qalabkan waxaa loo isticmaalaa in vitro lagu ogaado tayada helicobacter pylori nucleic acid ee muunado unug biopsy xuubka gastric xuubka ama muunado candhuufta bukaanada looga shakisan yahay in uu ku dhacay helicobacter pylori, oo waxay bixisaa hab kaaliyaha ogaanshaha bukaanka qaba cudurka helicobacter pylori.
Xirmada waxaa loo isticmaalaa in lagu ogaado tayada in vitro ee 28 nooc oo papillomaviruses ah (HPV6, 11, 16, 18, 26, 31, 33, 35, 39, 40, 42, 43, 44, 45, 51, 52,53) .
Qalabkan waxaa loogu talagalay in lagu ogaado tayada cudurada guud ee caabuqa kaadi mareenka, oo ay ku jiraan Neisseria gonorrhoeae (NG), Chlamydia trachomatis (CT), Ureaplasma urealyticum (UU), Herpes Simplex Virus Type 1 (HSV1), Herpes Simplex Virus Type 2 (HSV2) , Mycoplasma hominis (Mh), Mycoplasma genitalium (Mg) ee kaadi mareenka ragga iyo muunadaha dheecaanka xubinta taranka haweenka.
Qalabka HCV Quantitative Real-Time PCR Kit waa In vitro Nucleic Acid Test (NAT) si loo ogaado oo loo qiyaaso Hepatitis C Virus (HCV) asiidhyada nucleic ee ku jira balaasmaha dhiiga dadka ama muunadaha serum iyadoo la kaashanayo falcelinta silsilada tirooyinka dhabta ah ee wakhtiga dhabta ah (qPCR) ) habka.
Qalabkan waxa loo isticmaalaa in lagu ogaado teeb tayada leh nooca B, nooca C iyo nooca D ee muunadaha serum/balaasmaha ee fayraska cagaarshow B (HBV)
Qalabkan waxa loo isticmaalaa in vitro lagu ogaado tirada fayraska cagaarshowga B nucleic acid ee shaybaarada serum ee dadka.
Qalabkani wuxuu ku habboon yahay in lagu ogaado tayada cudur-sidaha caadiga ah ee caabuqyada urogenital ee ku jira vitro, oo ay ku jiraan Chlamydia trachomatis (CT), Ureaplasma urealyticum (UU), iyo Neisseria gonorrhoeae (NG).