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Imiba yeRheumatoid (RF)

Ukwazisa i-Aehealth RF Rapid Test Kit kunye ne-Aehealth FIA Meter, isisombululo sokusika esivela kwi-AEHEALTH LIMITED yokulinganisa ubungakanani be-RF (i-Rheumatoid Factor) kwigazi elipheleleyo lomntu, i-serum, okanye i-plasma. Le fluorescence immunoassay ibonelela ngeziphumo ezichanekileyo nezithembekileyo zokubhaqwa kweRF, umakisha ophambili ekuxilongeni nasekubekeni iliso kwizifo ezizimela ngokwazo ezifana ne-rheumatoid arthritis. Ikhithi yovavanyo olukhawulezayo kunye nemitha ye-FIA yenzelwe ukunikezela ngovavanyo olukhawulezayo nolusebenzayo, iyenza ilungele iilabhoratri zeklinikhi, izibhedlele kunye nezibonelelo zempilo. Ngojongano lwayo olusebenziseka lula kunye nobuchule obuchanekileyo bokulinganisa, i-Aehealth RF Rapid Test Kit ibonelela ngesisombululo esiluncedo nesisebenzayo kubasebenzi bezempilo ukuvavanya amanqanaba eRF ngokuzithemba. Thembela i-AEHEALTH LIMITED kwizisombululo ezitsha kuxilongo kunye neteknoloji yezempilo
  • Ixesha lokugcina 1. Gcina i-detector buffer ku-2~30°C. Isithinteli sizinzile ukuya kwiinyanga ezingama-24. 2. Gcina i-Aehealth RF Ikhasethi yovavanyo olukhawulezayo kwi-2 ~ 30 ° C, ubomi beshelufu bufikelela kwiinyanga ezingama-24.
  • IIMPAWU ZOKUSEBENZA Umda wokufumanisa: 10IU/mL; Uluhlu lomgca: 10-160IU / mL; I-coefficient yokulungelelanisa yomgca R ≥ 0.990; Ukuchaneka: ngaphakathi kwe-batch CV ngu ≤ 15%; phakathi kweebhetshi iCV yi ≤ 20%; Ukuchaneka: ukutenxa okunxulumene neziphumo zomlinganiselo akusayi kudlula ± 15% xa isilinganisi sokuchaneka esilungiswe ngumgangatho wesizwe weRF okanye isilinganisi sokuchaneka esisemgangathweni sivavanywa.