Pepsinogen I Pepsinogen II uye Gastrin-17 Combo yekukurumidza test kit
Diagnostic Kit yePepsinogen I/Pepsinogen II /Gastrin-17
Nzira: fluorescence immunochromatographic assay
Ruzivo rwekugadzira
| Model Number | G17/PGI/PGII | Packing | 25 Miedzo / kit, 30kits / CTN |
| Zita | Diagnostic Kit yePepsinogen I/Pepsinogen II /Gastrin-17 | Instrument classification | Kirasi II |
| Features | High senitivity, Easy operation | Chitupa | CE/ ISO13485 |
| Kururama | > 99% | Sherufu hupenyu | Makore maviri |
| Methodology | fluorescence immunochromatographic assay | OEM / ODM sevhisi | Avaliable |
ZVIRI KUSHANDISA
Iyi kit inoshanda kune in vitro quantitative yekuona kusungwa kwePepsinogen I (PGI), Pepsinogen II.
(PGII) uye Gastrin 17 mu serum yevanhu / plasma / yese yeropa samples, kuongorora gastric oxyntic gland cell.
basa, gastric fundus mucosa lesion uye atrophic gastritis. Iyo kit inopa chete bvunzo mhinduro yePepsinogen I
(PGI), Pepsinogen II (PGII) uye Gastrin 17. Chigumisiro chakawanikwa chichaongororwa pamwe chete nemamwe kliniki.
ruzivo. Inofanirwa kushandiswa chete nevashandi vehutano.
Test maitiro
| 1 | Usati washandisa reagent, verenga pasuru yacho nokungwarira uye uzvizivise nemafambisirwo ekushanda. |
| 2 | Sarudza yakajairika test mode yeWIZ-A101 inotakurika immune analyzer. |
| 3 | Vhura iyo aluminium foil bag package ye reagent uye tora bvunzo mudziyo. |
| 4 | Yakachinjika isa mudziyo wekuyedza mune slot ye immune analyzer. |
| 5 | Papeji rekutanga rekushandisa interface yeimmune analyzer, tinya "Standard" kuti upinde muyedzo interface |
| 6 | Dzvanya "QC Scan" kuti utarise kodhi yeQR padivi remukati rekiti; yekupinza kit inoenderana paramita mune chiridzwa uye sarudza rudzi rwemuenzaniso. Cherechedza: Nhamba yega yega yekiti yekiti ichaongororwa kwenguva imwe chete. Kana iyo batch nhamba yakaongororwa, saka svetuka danho iri. |
| 7 | Tarisa kuenderana kwe "Zita reChigadzirwa", "Batch Nhamba" nezvimwe. Pa test interface ine ruzivo rwekiti label. |
| 8 | Mushure mekunge kuenderana kweruzivo kwasimbiswa, tora sampuli diluent, wedzera 80µL ye serum / plasma / ropa rose. sampuli, uye zvakakwana sanganisa. |
| 9 | Wedzera 80µL yepamusoro yakasanganiswa mhinduro mune yemuenzaniso gomba rebvunzo mudziyo. |
| 10 | Mushure mekuwedzera sampuli yekuwedzera, tinya "Nguva" uye yasara nguva yekuyedza inozoratidzwa otomatiki pairi interface. |
| 11 | Immune analyzer inozopedzisa kuyedza uye kuongorora kana nguva yekuyedza yasvika. |
| 12 | Mhedzisiro kuverenga uye kuratidza Mushure mekunge bvunzo neimmune analyzer yapera, mhedzisiro yebvunzo inozoratidzwa pane test interface kana inogona kutariswa kuburikidza ne "Nhoroondo" pane peji reimba yekushanda interface. |
| Superiority Iyo kit ndeyechokwadi, inokurumidza uye inogona kutakurwa nekamuri tembiricha. Zviri nyore kushanda, nharembozha app inogona kubatsira mukududzira kwemhedzisiro uye kuichengeta kuti iite nyore kutevera. Muenzaniso wemhando: serum / plasma / sampuli dzeropa rose Nguva yekuedza: 10-15mins Kuchengetedza:2-30℃/36-86℉ Methodology:Solid Phase |
| Feature: • High sensitive • mhedzisiro kuverenga mumaminitsi gumi nemashanu • Easy operation • 2 miedzo munguva imwe chete |  |
Iyo Clinical Performance
Clinical evaluation performance yechigadzirwa inoongororwa nekuunganidza mazana maviri emakiriniki samples. Shandisa iyo yakashambadzirwa kititi ye enzyme yakabatana immunosorbent assay seye control reagent. Enzanisa iyo PGI bvunzo mhinduro. Shandisa mutsara regression kuongorora kuenzaniswa kwavo. Correlation coefficients yebvunzo mbiri ndeye y = 0.964X + 10.382 uye R=0.9763 zvakateerana. Enzanisa mhinduro dzePGII dzebvunzo. Shandisa mutsara regression kuongorora kuenzaniswa kwavo. Correlation coefficients yebvunzo mbiri ndeye y = 1.002X + 0.025 uye R=0.9848 zvakateerana. Enzanisa mhinduro dzebvunzo dzeG-17. Shandisa mutsara regression kuongorora kuenzaniswa kwavo. Correlation coefficients yebvunzo mbiri ndeye y = 0.983X + 0.079 uye R=0.9864 zvakateerana.
Unogonawo kuda:
