Colloidal Gold Blood Typhoid IgG/IgM Diagnostic Kit
I-Diagnostic Kit yeTyphoid IgG/IgM
Igolide yeColloidal
Ulwazi lwemveliso
| Inombolo yoMzekelo | Typhoid IgG/IgM | Ukupakisha | Iimvavanyo ze-25 / ikiti, i-20kits / i-CTN |
| Igama | I-Diagnostic Kit yeTyphoid IgG/IgM | Ukuhlelwa kwesixhobo | Iklasi Ii |
| Iimbonakalo | Uvakalelo oluphezulu, ukusebenza ngokulula | Isatifikethi | CE/ ISO13485 |
| Ukuchaneka | > 99% | Beka ubomi kwishelufa | Iminyaka emibini |
| Indlela yokusebenza | Igolide yeColloidal | Inkonzo ye-OEM/ODM | Iyafumaneka |
Inkqubo yovavanyo
| 1 | Khupha isixhobo sovavanyo kwisingxobo sefoyile esitywiniweyo usibeke kwindawo eyomileyo, ecocekileyo nethe tyaba |
| 2 | Qinisekisa ukuba ufakele ifowuni ngenombolo yesazisi yomzekelo |
| 3 | Gcwalisa i-pipette dropper kunye nomzekelo. Bamba idropha ngokuthe nkqo kwaye udlulisele ithontsi eli-1 legazi elipheleleyo/serum/isampuli yeplasma (malunga ne-10 μL) kwiqula lomfuziselo (S) , kwaye uqinisekise ukuba akukho amaqamza omoya. Emva koko yongeza amathontsi ama-3 esampuli yokuxutywa (malunga ne-80-100 μL) kwidiluent.kakuhle (D) ngoko nangoko. Jonga umfanekiso ongezantsi. |
| 4 | Qala isibali-xesha. |
| 5 | Lindela ukuba umgca onemibala ibonakale. Funda iziphumo zovavanyo ngemizuzu eyi-15. Iziphumo ezincomekayo zinokubonakala ngomzuzu om-1. Iziphumo ezimbi mazingqinwe ekupheleni kwemizuzu eyi-20 kuphela. Musa ukutolika umphumo emva kwemizuzu engama-20. |
Injongo yokuSebenzisa
I-Diagnostic Kit ye-Typhoid IgG / IgM (i-Colloidal Gold) yinkqubo ekhawulezayo, ye-serological, i-lateral flow chromatographic immunoassay eyenzelwe ukufumanisa ngaxeshanye kunye nokwahlukana kwe-anti-Salmonella typhi (S.typhi) IgG kunye ne-IgM kwigazi elipheleleyo lomntu, i-serum okanye i-plasma isampuli. Yenzelwe ukusetyenziswa ngabasebenzi bezempilo njengovavanyo lokuhlola kunye noncedo ekuxilongeni ukosuleleka yi-S. typhi. Uvavanyo lubonelela ngeziphumo zohlalutyo lwangaphambili kwaye alusebenzi njengenqobo eqinisekileyo yokuxilongwa. Nakuphi na ukusetyenziswa okanye ukutolikwa kovavanyo kufuneka kuhlalutywe kwaye kuqinisekiswe ngenye indlela (ii) zovavanyo kunye neziphumo zeklinikhi ezisekelwe kwisigwebo sobuchule sababoneleli bezempilo.
Ukongama
Ixesha lokuvavanya: imizuzu eyi-15
Ugcino:2-30℃/36-86℉
Indlela yokusebenza:Igolide yeColloidal
Isatifikethi seCFDA
Uphawu:
• Uvakalelo oluphezulu
• iziphumo zokufunda kwimizuzu eli-15
• Ukusebenza ngokulula
• Ixabiso elithe ngqo kwifektri
• Awudingi umatshini owongezelelweyo wokufunda iziphumo
Ukufundwa kweziphumo
Uvavanyo oluKhawulezayo lweTyphoid IgG/IgM luye lwavavanywa ngereferensi yovavanyo lwe-ELISA yorhwebo kusetyenziswa iisampulu zeklinikhi. Iziphumo zovavanyo zinikwe kolu luhlu lungezantsi:
Ukusebenza kweklinikhi ye-anti-S. typhi IgM Test
| Iziphumo zeWIZ zeTyphoid IgG/IgM | S. typhi Uvavanyo lwe-IgM ELISA | Uvakalelo (IsiVumelwano sePesenti eNgcono): 93.93% = 31/33 (95% CI: 80.39% ~ 98.32%) Ukuchaneka (Negative Percent Agreement): 99.52% = 209/210 (95% CI: 93.75% ~ 99.92%) Ukuchaneka (IsiVumelwano Sepesenti Sisonke): 98.76% = (31+209)/243 (95% CI: 96.43% ~ 99.58%) | ||
| Okuhle | Ibi | Iyonke | ||
| Okuhle | 31 | 1 | 32 | |
| Ibi | 2 | 209 | 211 | |
| Iyonke | 33 | 210 | 243 | |
Ukusebenza kweklinikhi ye-anti-S. typhi Uvavanyo lwe-IgG
| Iziphumo zeWIZ zeTyphoid IgG/IgM | S. typhi IgG ELISA Uvavanyo | Uvakalelo (IsiVumelwano sePesenti eNgcono): 88.57% = 31/35 (95% CI: 74.05% ~ 95.46%) Ukuchaneka (Negative Percent Agreement): 99.54% = 219/220 (95% CI: 97.47% ~ 99.92%) Ukuchaneka (IsiVumelwano Sepesenti Sisonke): 98.03% = (31+219)/255 (95% CI: 95.49% ~ 99.16%) | ||
| Okuhle | Ibi | Iyonke | ||
| Okuhle | 31 | 1 | 32 | |
| Ibi | 4 | 219 | 223 | |
| Iyonke | 35 | 220 | 255 | |
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