Ulawulo lwesifo seswekile Ikhithi yokuDinga i-insulin
Ikhithi yokuxilonga kwi-insulin
Indlela yokusebenza:Fluorescence Immunochromatographic Assay
Ulwazi lwemveliso
| Inombolo yoMfanekiso | INS | Ukupakisha | Iimvavanyo ze-25 / ikiti, i-30kits / i-CTN |
| Igama | Ikhithi yokuxilonga kwi-insulin | Ukuhlelwa kwesixhobo | Iklasi Ii |
| Iimbonakalo | Uvakalelo oluphezulu, ukusebenza ngokulula | Isatifikethi | CE/ ISO13485 |
| Ukuchaneka | > 99% | Beka ubomi kwishelufa | Iminyaka emibini |
| Indlela yokusebenza | Fluorescence Immunochromatographic Assay | Inkonzo ye-OEM/ODM | Iyafumaneka |
Ukongama
Ixesha lokuvavanya: 10-15mins
Ugcino:2-30℃/36-86℉
Indlela yokusebenza:Fluorescence Immunochromatographic Assay
Uphawu:
• Uvakalelo oluphezulu
• iziphumo zokufunda kwimizuzu eli-15
• Ukusebenza ngokulula
• Ukuchaneka okuphezulu
UKUSETYENZISWA OKUHLOSIWEYO
Le kit ifanelekile kwi-in vitro quantitative determination of insulin (INS) amanqanaba kwi-serum yabantu / i-plasma / iisampulu zegazi elipheleleyo ukuze kuhlolwe umsebenzi we-pancreatic-islet β-cell. Le khithi ibonelela kuphela iziphumo zovavanyo lwe-insulin (INS), kwaye umphumo ofunyenweyo uya kuhlalutywa ngokudibeneyo kunye nolunye ulwazi lweklinikhi. Isiphumo siya kuhlalutywa ngokudityaniswa nolunye ulwazi lweklinikhi.
Inkqubo yovavanyo
| 1 | Ngaphambi kokusebenzisa i-reagent, funda iphakheji efakwe ngononophelo kwaye uziqhelanise neenkqubo zokusebenza. |
| 2 | Khetha imo yovavanyo oluqhelekileyo lwe-WIZ-A101 ye-immune analyzer ephathekayo |
| 3 | Vula i-aluminium foil bag package ye-reagent kwaye ukhuphe isixhobo sovavanyo. |
| 4 | Faka ngokuthe tye isixhobo sovavanyo kwi-slot ye-immune analyzer. |
| 5 | Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-"Standard" ukufaka ujongano lovavanyo. |
| 6 | Cofa "QC Scan" ukuskena ikhowudi ye-QR kwicala langaphakathi lekhithi; igalelo kit ezinxulumene parameters kwisixhobo kwaye ukhethe uhlobo isampuli. Qaphela: Inani lebhetshi nganye yekhithi iya kuskenwa ngexesha elinye. Ukuba inombolo yebhetshi iskeniwe, uze utsibe eli nyathelo. |
| 7 | Khangela ukuhambelana "kweGama leMveliso", "Inombolo yeBatch" njl. |
| 8 | Thatha isampulu yediluent kulwazi olungaguqukiyo, yongeza i-10μL serum/plasma/isampulu yegazi elipheleleyo, kwaye uzixube kakuhle; |
| 9 | Yongeza i-80µL echazwe ngasentla isisombululo esixutywe kakuhle kwiqula lesixhobo sovavanyo; |
| 10 | Emva kokudibanisa isampulu epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liya kuboniswa ngokuzenzekelayo kujongano. |
| 11 | Umhlalutyi we-Immune uya kugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lokuvavanya lifikelelwe. |
| 12 | Emva kokuba uvavanyo lwe-immune analyser lugqityiwe, iziphumo zovavanyo ziya kuboniswa kujongano lovavanyo okanye zinokujongwa “ngeMbali” kwiphepha lasekhaya lojongano lokusebenza. |
Qaphela: isampuli nganye iya kubhobhozwa ngepayipi ecocekileyo elahlwayo ukuphepha ukungcoliseka komnqamlezo.
Ukusebenza kweklinikhi
Ukusebenza kovavanyo lweklinikhi kule mveliso kwavavanywa ngokuqokelela iisampulu zeklinikhi ezili-173. Iziphumo zeemvavanyo zifaniswa kusetyenziswa iikiti ezihambelanayo zendlela yokuthengisa i-electrochemiluminescence njenge-reagents yereferensi, kwaye ukuthelekiswa kwabo kwaphandwa ngokuguqulwa komgca, kwaye i-coefficients yokulungelelaniswa kweemvavanyo ezimbini y = 0.987x + 4.401 kunye ne-R = 0.9874, ngokulandelanayo. .
