Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus
Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus
(Uvavanyo lwe-Fluorescence Immunochromatomatographic)
Ulwazi lwemveliso
| Inombolo yoMzekelo | P24 | Ukupakisha | Iimvavanyo ezingama-25/ikhithi, iikhithi ezingama-30/i-CTN |
| Igama | Ikhithi yokuxilonga ye-P24 Antigen ukuya kwi-Human Immunodeficiency Virus | Iisixhobo somculoudidi lwe-t | Iklasi yesi-3 |
| Iimbonakalo | Uvakalelo oluphezulu, Ukusebenza lula | Isatifikethi | I-CE/I-ISO13485 |
| Ukuchaneka | > 99% | Beka ubomi kwishelufa | Iminyaka emibini |
| Indlela yokusebenza | (Uvavanyo lwe-Fluorescence Immunochromatomatographic) | Inkonzo ye-OEM/ODM | Iyafumaneka |
Inkqubo yovavanyo
| 1 | Vula iphakheji ye-reagent yebhegi yefoyile ye-aluminiyam, uze ukhuphe isixhobo sovavanyo; |
| 2 | Faka isixhobo sovavanyo ngokuthe tye kwindawo yokuhlaziya umzimba; |
| 3 | Kwiphepha lasekhaya le-interface yokusebenza ye-immune analyzer, cofa u-“Standard” ukuze ufake i-interface yovavanyo; |
| 4 | Cofa u-“QC Scan” ukuze uskene ikhowudi ye-QR kwicala langaphakathi lekhithi; iiparameter ezinxulumene nekhithi yokufaka kwisixhobo, kwaye ukhethe uhlobo lwesampulu; |
| 5 | Jonga ukuhambelana kwe-“Product Name”, “Batch Number” njl. njl. kwi-interface yovavanyo ngolwazi olukwileyibhile yekhithi; |
| 6 | Emva kokuba ulwazi luqinisekisiwe, khupha izinto zokucoca isampuli, yongeza i-80µL yesampuli yeserum, uze uyixube ngokwaneleyo; |
| 7 | Yongeza i-80µL yesisombululo esixutyiweyo esingentla kumngxuma wesampulu yesixhobo sovavanyo; |
| 8 | Emva kokongeza isampuli epheleleyo, cofa u-“Timing” kwaye ixesha eliseleyo lovavanyo liza kuboniswa ngokuzenzekelayo kwi-interface. |
| 9 | I-immune analyzer iza kugqiba uvavanyo kunye nohlalutyo ngokuzenzekelayo xa ixesha lovavanyo lifikile. |
Injongo Yokusebenzisa
Le khithi ifanelekile kwi-in vitroubungakananiukufunyanwa kwe-antigen ye-human immunodeficiency virus (p24) kwisampuli ye-serum yomntu njengoncedo ekuxilongweni kosulelo lwe-human immunodeficiency virus. Le khithi inika iziphumo zokufunyanwa kwe-human immunodeficiency virus antigen (p24) kuphela kwaye iziphumo ezifunyenweyo ziya kuhlaziywa kunye nolunye ulwazi lweklinikhi.
Isishwankathelo
I-Human Immunodeficiency Virus (HIV) ikwi-genus Lentivirus kusapho lweRetroviridae kwaye yimbangela ye-Acquired Immunodeficiency Syndrome (AIDS), ehlulwe ngohlobo 1 kunye nohlobo 2 kuxhomekeke kwimvelaphi yemfuza yentsholongwane. Uhlobo 1 kunye nohlobo 2 zihlulwe ngokwemvelaphi yemfuza yentsholongwane. Iindlela eziphambili zokudlulisela intsholongwane yi-HIV kukudlulisela ngesondo, ukudluliselwa kwegazi kunye nokudluliselwa komntwana ngumama. Kwiiveki ezi-1-2 emva kosulelo lwe-HIV, uphawu lokuqala lwentsholongwane egazini yiproteni ephambili ye-p24.
Uphawu:
• Uvakalelo oluphezulu
• ukufundwa kweziphumo kwimizuzu eli-15
• Ukusebenza okulula
• Ixabiso elithe ngqo lefektri
• Andidingi matshini wongezelelweyo ukuze ndifunde iziphumo
Ukusebenza kweklinikhi
Uvavanyo lweklinikhi lokusebenza kwemveliso luvavanywa ngokuqokelela330 iisampulu zeklinikhi. Ikhithi ehambelanayo yendlela ye-electrochemiluminescence edwelisiweyo isetyenziswa njenge-reagent yokulawula. Iziphumo zovavanyo ziyathelekiswa, kwaye ukuthelekiswa kwazo kufundwa nge-linearity regression. Ii-coefficients zokunxibelelana kwezi vavanyo zimbini zeziY=0998X+0.380 kunye ne-R=0.9889, ngokulandelelana.
Ungathanda kwakhona:
I-HCV
Ikhithi yoVavanyo oluKhawulezayo lwe-HCV yeNyathelo elinye Ikhithi yoVavanyo oluKhawulezayo lwe-Hepatitis C Virus Antibody














