I-Malaria PF Rapid Test Colloidal Gold ngemvume ye-CE

incazelo emfushane:

Umalaleveva PF Rapid Test Colloidal Gold

 


  • Isikhathi sokuhlola:10-15 imizuzu
  • Isikhathi esivumelekile:Izinyanga ezingama-24
  • Ukunemba:Ngaphezu kuka-99%
  • Ukucaciswa:1/25 ukuhlolwa/ibhokisi
  • Izinga lokushisa lesitoreji :2℃-30℃
  • Indlela yokwenza:Igolide le-Colloidal
  • Imininingwane Yomkhiqizo

    Omaka bomkhiqizo

    Umalaleveva PF Rapid Test Colloidal Gold

    Ulwazi lokukhiqiza

    Inombolo Yemodeli Umalaleveva PF Ukupakisha 25 Ukuhlolwa/ikhithi, 30kits/CTN
    Igama

    Umalaleveva PF Rapid Test Colloidal Gold

    Ukuhlukaniswa kwezinsimbi Ikilasi I
    Izici Ukuzwela okuphezulu, ukusebenza okulula Isitifiketi CE/ ISO13485
    Ukunemba > 99% Impilo yeshelufu Iminyaka Emibili
    Indlela yokwenza Igolide le-Colloidal Isevisi ye-OEM/ODM Iyatholakala

     

    Inqubo yokuhlola

    1 Buyisela isampula nekhithi kuthempelesha yegumbi, khipha idivayisi yokuhlola esikhwameni esivaliwe, bese uyilalisa ebhentshini elivundlile.
    2 I-Pipette 1 yehla (cishe ku-5μL) yesampula yegazi lonke emthonjeni wedivayisi yokuhlola ('S') ngokuma futhi kancane ngepayipi elahlwayo elinikeziwe.
    3 Guqula isampula uyibhekise phansi, ulahle amaconsi amabili okuqala e-diluent yesampula, engeza amaconsi angu-3-4 esampuli engenabhamuza ehlanjululwe ngokudonsa phansi emthonjeni wedivayisi yokuhlola ('D' kahle) uqonde futhi kancane, bese uqala ukubala isikhathi.
    4 Umphumela uzohunyushwa phakathi kwemizuzu eyi-15 ~ 20, futhi umphumela wokutholwa awuvumelekile ngemuva kwemizuzu engama-20.

    Qaphela:: isampula ngayinye izofakwa ngepayipi ngepayipi elahlwayo elihlanzekile ukuze kugwenywe ukungcoliswa okuphambanayo.

    Ihlose Ukusebenzisa

    Le khithi isebenza ekutholweni kwekhwalithi ye-in vitro ye-antigen ku-plasmodium falciparum histidine-rich proteins II (HRP II), futhi isetshenziselwa ukuxilonga okuwusizo kokutheleleka nge-plasmodium falciparum (pf).Le kit inikeza kuphela umphumela wokuthola ama-antigen amaprotheni e-histidine II (HRP II), futhi imiphumela etholiwe izosetshenziswa ngokuhambisana nolunye ulwazi lomtholampilo ukuze luhlaziywe.Kufanele isetshenziswe kuphela ochwepheshe bezempilo.

    I-HIV

    Isifinyezo

    Umalaleveva ubangelwa amagciwane anengqamuzana elilodwa eqembu le-plasmodium, ngokuvamile usakazwa ngokulunywa omiyane, futhi isifo esithathelwanayo esithinta izimpilo nokuphepha kwempilo yabantu nezinye izilwane.Iziguli ezitheleleke ngomalaleveva ngokuvamile zizoba nomkhuhlane, ukukhathala, ukuhlanza, ikhanda elibuhlungu nezinye izimpawu, futhi izimo ezinzima zingaholela ku-xanthoderma, isithuthwane, i-coma ngisho nokufa.Ukuhlola Okusheshayo Umalaleveva (PF) kungathola ngokushesha i-antigen kuya ku-plasmodium falciparum histidine-rich proteins II ephuma egazini lilonke, engasetshenziswa ekuxilongeni okusizayo kokutheleleka nge-plasmodium falciparum (pf).

     

    Isici:

    • Ukuzwela okuphezulu

    • umphumela wokufunda emizuzwini eyi-15

    • Ukusebenza okulula

    • Intengo eqondile yasefekthri

    • Awudingi umshini owengeziwe wokufunda imiphumela

     

    Ikhithi ye-HIV rapiddiagnosis
    umphumela wokuhlolwa

    Ukufundwa kwemiphumela

    Ukuhlolwa kwe-reagent ye-WIZ BIOTECH kuzoqhathaniswa ne-reagent yokulawula:

    Ireferensi Ukuzwela Ukucaciswa
    I-reagent eyaziwayo PF98.54%, iPan:99.2% 99.12%

     

    Ukuzwela:PF98.54%,Pan.:99.2%

    Ukucaciswa:99.12%

    Ungase futhi uthande:

    I-HCV

    Ikhithi Yokuhlola Okusheshayo ye-HCV Isinyathelo esisodwa se-Hepatitis C Virus Antibody Rapid Test Kit

     

    Hp-Ag

    Ikhithi Yokuxilonga Ye-Antigen Iya ku-Helicobacter Pylori (HP-AG) Nge-CE Evunyiwe

    VD

    Ikhithi Yokuxilonga 25-(OH)VD TEST Kit Quantitative Kit POCT Reagent


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