Ikhasethi yoVavanyo oluKhawulezayo lweHCV (WB/S/P)
HCV Rapid Test Cassette/Strip/kit (WB/S/P)
[OKUHLOSIWEYO UKUSETYENZISWA]
I-HCV Rapid Test Cassette/Strip is a lateral flow chromatographic immunoassay for the qualitative monitor of antibodies to Hepatitis C Virus in Whole Blood/Serum/Plasma.Ibonelela ngoncedo ekuxilongeni usulelo nge-Hepatitis C Virus.
[USHWANKATHELO]
Intsholongwane ye-Hepatitis C (HCV) yintsholongwane ye-RNA enemitya enye yosapho lwe-Flaviviridae kwaye iyi-agent ebangela i-Hepatitis C. I-Hepatitis C sisifo esingapheliyo esichaphazela malunga ne-130-170 yezigidi zabantu kwihlabathi jikelele.Ngokutsho kwe-WHO, ngonyaka, abantu abangaphezu kwe-350,000 bafa ngenxa yezifo zesibindi ezinxulumene ne-hepatitis C kunye ne-3-4 yezigidi zabantu bosulelwa yi-HCV.Malunga ne-3% yabemi behlabathi kuqikelelwa ukuba bosulelwe yi-HCV.Ngaphezu kwe-80% yabantu abosulelwe yi-HCV bahlakulela izifo zesibindi ezingapheliyo, i-20-30% ikhula i-cirrhosis emva kwe-20-30 yr, kwaye i-1-4% ibulawa yi-cirrhosis okanye umhlaza wesibindi.Abantu abosulelwe yi-HCV bavelisa izilwa-buhlungu zentsholongwane kwaye ubukho bezi zithinteli-gazi egazini bubonisa usulelo lwangoku okanye lwangaphambili lweHCV.
[UHLELO](25sets/ 40sets/50sets/customized specifications zonke zivunyiwe)
Ikhasethi yovavanyo/istrip iqulethe i-membrane strip eqatywe nge-antigen ye-HCV edityanisiweyo kumgca wovavanyo, i-antibody yomvundla kumgca wolawulo, kunye nephedi yedayi equlethe igolide ye-colloidal edityaniswe ne-antigen ye-HCV ephinda ihlanganiswe.Ubungakanani beemvavanyo zaprintwa kwiileyibhile.
Izinto eziphathekayo Kubonelelwe
Uvavanyo lwekhasethi/umcu
Faka iphakheji
Isithinteli
Izinto Eziyimfuneko Kodwa Ezingabonelelwanga
Isingxobo sokuqokelelwa kwesampuli
Isibali-xesha
Iindlela eziqhelekileyo ziyasilela ukuyibeka yodwa intsholongwane kwinkcubeko yeeseli okanye ukuyibona nge-electron microscope.Ukudibanisa i-genome yentsholongwane kwenze ukuba kube lula ukuphuhlisa iimvavanyo ze-serologic ezisebenzisa i-antigens eziphinda ziphinde zibuyele.Xa kuthelekiswa nesizukulwana sokuqala se-HCV EIA sisebenzisa i-antigen enye ephinda iphinde yaphinda yaphinda yaphinda, ii-antigens ezininzi ezisebenzisa iprotein ephinda-phindayo kunye/okanye iipeptide zokwenziwa ziye zongezwa kuvavanyo olutsha lwe-serologic ukunqanda ukuphambana okungaqhelekanga kunye nokwandisa ubuntununtunu bovavanyo lwe-antibody ye-HCV.I-HCV Rapid Test Cassette/Strip ibhaqa izilwa-buhlungu kusulelo lwe-HCV kwi-Whole Blood/Serum/Plasma.Uvavanyo lusebenzisa indibanisela yeprotheyini A amasuntswana agqunyiweyo kunye neeproteni ze-HCV eziphinda-phindane nazo ukuze zibone ngokukhethiweyo izilwa-buhlungu ze-HCV.Iiprotheni ze-HCV ezihlaziyiweyo ezisetyenzisiweyo kuvavanyo zifakwe kwikhowudi yezofuzo zombini i-structural (nucleocapsid) kunye neeprotheni ezingezizo.
[UMGAQO]
I-HCV Rapid Test Cassette / Strip yi-immunoassay esekelwe kumgaqo we-double antigen-sandwich technique.Ngexesha lovavanyo, iGazi eliPheleleyo/iSerum/i-Plasma isampula ifudukela phezulu ngesenzo se-capillary.Izilwa-buhlungu kwi-HCV ukuba zikhona kwi-specimen ziya kubophelela kwi-HCV conjugates.I-immune complex iyabanjwa kwi-membrane yi-antigens ye-HCV efakwe ngaphambili, kwaye umgca ombala obonakalayo uya kubonakala kummandla wovavanyo obonisa umphumo omuhle.Ukuba ii-antibodies kwi-HCV azikho okanye zikhona ngaphantsi kwenqanaba elibonakalayo, umgca onemibala awuyi kubumba kwingingqi yovavanyo olubonisa umphumo ombi.
Ukuze usebenze njengolawulo lwenkqubo, umgca onemibala uya kuhlala ubonakala kwindawo yolawulo, ebonisa ukuba umthamo ofanelekileyo we-specimen wongeziwe kwaye i-membrane wicking yenzeke.
(Umfanekiso ngowereferensi kuphela, nceda ubhekisele kwinto ebonakalayo.) [YeCassette]
Susa ikhasethi yovavanyo kwisingxobo esivaliweyo.
Kwi-serum okanye i-plasma specimen: Bamba i-dropper ngokuthe nkqo kwaye udlulisele amathontsi ama-3 e-serum okanye iplasma (malunga ne-100μl) kumzekelo wequla (S) lesixhobo sovavanyo, emva koko uqalise isibali-xesha.Jonga umfanekiso ongezantsi.
Ngeesampuli zegazi elipheleleyo: Bamba idropha ngokuthe nkqo kwaye udlulisele ithontsi eli-1 legazi elipheleleyo (malunga ne-35μl) kumzekelo wequla (S) lesixhobo sovavanyo, emva koko wongeze amathontsi ama-2 e-buffer (malunga ne-70μl) kwaye uqalise isibali-xesha.Jonga umfanekiso ongezantsi.
Linda i(imi)layini enemibala ibonakale.Ukutolika iziphumo zovavanyo kwimizuzu eyi-15.Sukuzifunda iziphumo emva kwemizuzu engama-20.
[IZILUMKISO KUNYE NEMIGAQO]
Ukusetyenziswa kwe-in vitro diagnostic kuphela.
Kubasebenzi bezempilo kunye neengcali kwindawo yeendawo zokhathalelo.
Musa ukusebenzisa emva komhla wokuphelelwa.
Nceda ufunde lonke ulwazi olukweli phetshana phambi kokuba wenze uvavanyo.
Ikhasethi yovavanyo/umcu kufuneka uhlale kwisingxobo esitywiniweyo de usetyenziswe.
Yonke imizekelo kufuneka ithathwe njengeyingozi kwaye iphathwe ngendlela efanayo ne-arhente eyosulelayo.
Ikhasethi yovavanyo esetyenzisiweyo/istrip kufuneka ilahlwe ngokwe- federal, state and local rules.
[ULAWULO LWEMEKO]
Ulawulo lwenkqubo lufakiwe kuvavanyo.Umgca wombala ovela kummandla wolawulo (C) uthathwa njengolawulo lwangaphakathi lwenkqubo.Iqinisekisa umthamo owaneleyo we-specimen, i-membrane eyaneleyo ye-wicking kunye nobuchule obuchanekileyo benkqubo.
Imigangatho yolawulo ayibonelelwanga nale khithi.Nangona kunjalo, kucetyiswa ukuba ulawulo oluqinisekileyo kunye nolungalunganga luvavanywe njengenkqubo efanelekileyo yaselabhoratri ukuqinisekisa inkqubo yovavanyo kunye nokuqinisekisa ukusebenza ngokufanelekileyo kovavanyo.
[IMIDA]
I-HCV Rapid Test Cassette/Strip ilinganiselwe ukunika ubhaqo olusemgangathweni.Ubunzulu bomgca wovavanyo abudibanisi nokuxinana kwe-antibody egazini.
Iziphumo ezifunyenwe kolu vavanyo zenzelwe ukuba zibe luncedo ekuxilongeni kuphela.Ugqirha ngamnye kufuneka atolike iziphumo ngokubambisana nembali yesigulane, ukufunyaniswa komzimba, kunye nezinye iinkqubo zokuxilonga.
Iziphumo zovavanyo olubi zibonisa ukuba amajoni omzimba kwi-HCV mhlawumbi abekho okanye akumanqanaba angabonwa luvavanyo.
[IIMPAWU ZOKUSEBENZA]
Ukuchaneka
Isivumelwano noVavanyo oluKhawulezayo lwe-HCV yoRhwebo
Uthelekiso olusecaleni lwenziwe kusetyenziswa uVavanyo oluKhawulezileyo lwe-HCV kunye novavanyo olukhawulezileyo lwe-HCV olufumaneka ngokurhweba.Iisampuli zeklinikhi ezili-1035 ezivela kwizibhedlele ezithathu zavavanywa ngoVavanyo oluKhawulezayo lwe-HCV kunye nekiti yorhwebo.Iisampulu zajongwa nge-RIBA ukuqinisekisa ubukho be-antibody ye-HCV kwisampulu.Ezi ziphumo zilandelayo zidweliswe kolu phando lwezonyango:
| UVavanyo oluKhawulezayo lweHCV yoRhwebo | Iyonke | |||
| Okuhle | Ibi | |||
| I-HEO TECH® | Okuhle | 314 | 0 | 314 |
| Ibi | 0 | 721 | 721 | |
| Iyonke | 314 | 721 | 1035 | |
Isivumelwano phakathi kwezi zixhobo zimbini yi-100% yeesampulu ezilungileyo, kunye ne-100% yeempawu ezimbi.Olu phononongo lubonise ukuba i-HCV Rapid Test ilingana kakhulu nesixhobo sorhwebo.
Isivumelwano neRIBA
Iisampuli zekliniki ezingama-300 zavavanywa ngoVavanyo oluKhawulezayo lwe-HCV kunye nekhithi ye-HCV RIBA.Ezi ziphumo zilandelayo zidweliswe kolu phando lwezonyango:
| I-RIBA | Iyonke | |||
| Okuhle | Ibi | |||
| I-HEO TECH® | Okuhle | 98 | 0 | 98 |
| Ibi | 2 | 200 | 202 | |
| Iyonke | 100 | 200 | 300 | |
