Ikhithi yokuxilonga yekhithi yovavanyo lweCardiac Troponin T Rapid
Ikhithi yokuxilonga yeCardiac Troponin T
Indlela yokusebenza: Uvavanyo lwe-Fluorescence Immunochromatographic
Ulwazi lwemveliso
| Inombolo yoMzekelo | i-cTnT | Ukupakisha | Iimvavanyo ezingama-25/ikhithi, iikhithi ezingama-30/i-CTN |
| Igama | Ikhithi yokuxilonga yeCardiac Troponin T | Ukuhlelwa kwezixhobo | Iklasi yesiBini |
| Iimbonakalo | Uvakalelo oluphezulu, Ukusebenza lula | Isatifikethi | I-CE/ ISO13485 |
| Ukuchaneka | > 99% | Beka ubomi kwishelufa | Iminyaka emibini |
| Indlela yokusebenza | Uvavanyo lwe-Fluorescence Immunochromatographic | Inkonzo ye-OEM/ODM | Iyafumaneka |
UKUSETYENZISWA OKUJOLISWEYO
Le khithi yenzelwe ukufumanisa ubungakanani be-in vitro kumxholo we-cardiac troponin T (cTnT) kwi-serum/plasma/isampulu yegazi elipheleleyo lomntu kwaye yenzelwe ukuxilongwa okuncedisayo kwe-acute myocardial infarction. Le khithi inika kuphela iziphumo zovavanyo lwe-cardiac troponin T (cTnT), kwaye iziphumo ezifunyenweyo ziya kuhlaziywa kunye nolunye ulwazi lweklinikhi.
Inkqubo yovavanyo
| 1 | Ngaphambi kokusebenzisa i-reagent, funda ngononophelo iphakheji kwaye uqhelane neenkqubo zokusebenza. |
| 2 | Khetha imo yovavanyo oluqhelekileyo lwe-WIZ-A101 portable immune analyzer |
| 3 | Vula iphakheji ye-reagent yebhegi yefoyile ye-aluminiyam uze ukhuphe isixhobo sovavanyo. |
| 4 | Faka isixhobo sovavanyo ngokuthe tye kwindawo yokuhlaziya umzimba. |
| 5 | Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-“Standard” ukuze ufake i-interface yovavanyo. |
| 6 | Cofa u-“QC Scan” ukuze uskene ikhowudi ye-QR ngaphakathi kwekhithi; faka iiparameter ezinxulumene nekhithi kwisixhobo kwaye ukhethe uhlobo lwesampulu. Qaphela: Inani ngalinye lebhetshi yekhithi kufuneka liskeniwe kube kanye. Ukuba inani lebhetshi liskeniwe, yitsibe le nyathelo. |
| 7 | Jonga ukuhambelana kwe "Igama leMveliso", "Inombolo yeBatch" njl. njl. kwi-interface yovavanyo kunye nolwazi olukwileyibhile yekhithi. |
| 8 | Thatha isampuli ye-diluent xa ufumene ulwazi olufanayo, yongeza i-80μL serum/plasma/isampuli yegazi elipheleleyo, uze uyixube kakuhle; |
| 9 | Yongeza isisombululo esixutywe kakuhle esingama-80µL emthonjeni wesixhobo sovavanyo; |
| 10 | Emva kokongeza isampuli epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liza kuboniswa ngokuzenzekelayo kwi-interface. |
| 11 | I-immune analyzer izakugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lovavanyo lifikile. |
| 12 | Emva kokuba uvavanyo lwe-immune analyzer lugqityiwe, iziphumo zovavanyo ziya kuboniswa kwi-interface yovavanyo okanye zinokujongwa "kwiMbali" kwiphepha lasekhaya le-interface yokusebenza. |
Qaphela: isampulu nganye mayifakwe ngepayipi ecocekileyo elahlwayo ukuze kuthintelwe ungcoliseko oluhambelanayo.
Ukubaluleka
Ixesha lovavanyo: 10-15mins
Indawo yokugcina: 2-30℃/36-86℉
Indlela yokusebenza: Uvavanyo lwe-Fluorescence Immunochromatographic
Uphawu:
• Uvakalelo oluphezulu
• ukufundwa kweziphumo kwimizuzu eli-15
• Ukusebenza okulula
• Uvavanyo olu-3 ngexesha elinye, okonga amaxesha.
• Ukuchaneka Okuphezulu
Ukusebenza kweKlinikhi
Uvavanyo lweklinikhi lokusebenza kwemveliso luvavanywa ngokuqokelela150iisampulu zeklinikhi. Sebenzisa ikhithi ye-ECLIA ethengiswayo ehambelanayo njenge-reagent yokulawula kwaye uthelekise iziphumo zovavanyo. Sebenzisa ukuhlehla okuthe ngqo ukuphanda ukuthelekiswa kwazo. Ii-coefficients zokunxibelelana kwezi vavanyo zimbini yi-Y=101X-20.585kunye ne-R=0.9844, ngokulandelelana.
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