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Uvakalelo oluphezulu lweCardiac troponin I(Hs-cTnI)

Ukwazisa nge-hs-cTnI Rapid Quantitative Test, ngokubambisana ne-Aehealth FIA Meter, yi-AEHEALTH LIMITED. Le mveliso entsha yenzelwe ukuzimisela okuchanekileyo kunye nokukhawuleza kweCardiac troponin I (cTnI) kwigazi elipheleleyo lomntu, i-serum, okanye i-plasma. I-high-sensitivity yolu vavanyo yenza ukuba ibe sisixhobo esixabisekileyo sokuxilongwa kwe-myocardial infarction, ukunceda abaqeqeshi bezempilo ekwenzeni izigqibo ezibalulekileyo zokunyamekela isigulane. Uvavanyo lubonelela ngeziphumo zobungakanani obuchanekileyo, luvumela uhlolo olukhawulezayo nolusebenzayo lwamanqanaba e-cTnI. Nge-Aehealth FIA Meter, i-hs-cTnI Rapid Quantitative Test inikezela ngesisombululo esisebenzisekayo nesithembekileyo kwizibonelelo zempilo. Ukuthembela kwi-AEHEALTH LIMITED malunga neemveliso zokuxilonga ezikumgangatho ophezulu ukuxhasa iziphumo eziphuculweyo zesigulana.

  • Ixesha lokugcina 1. Gcina i-detector buffer ku-2~30°C. Isithinteli sizinzile ukuya kwiinyanga ezingama-24. 2. Gcina i-Aehealth hs-cTnI Ikhasethi yovavanyo olukhawulezayo kwi-2 ~ 30 ° C, ubomi beshelufu bufikelela kwiinyanga ezingama-24.
  • IIMPAWU ZOKUSEBENZA Umda wokufumanisa: 0.01ng / mL; Uluhlu lomgca: 0.01 ~ 20.00 ng / 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 isikali sokuchaneka esilungiswe ngumgangatho wesizwe we-cTnI okanye isilinganisi sokuchaneka esisemgangathweni sivavanywa.