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 elilahlwayo 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 okuyisizayo 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 aneseli elilodwa eqembu le-plasmodium, ngokuvamile usakazwa ukulunywa 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. Ukuhlolwa 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 yokuhlola i-HIV ngokushesha
    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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